Name:Propitocaine hcl
CAS:1786-81-8
Assay:>99%
Appearance:white powder
Name
Propitocaine hcl
Synonyms
2-(Propylamino)-o-propionotoluidide hydrochloride; N-(2-Methylphenyl)-2-(propylamino)-propanamide hcl
Molecular Formula
C
13
H
20
N
2
O
.
HCl
Molecular Weight
256.77
CAS Registry Number
1786-81-8
EINECS
217-244-0
Tuesday, September 6, 2011
Terbinafine Hydrochioride
As a manufacture, we can offer you our lowest price but competitive quality.
Terbinafine Hydrochloride
Antifungal, allylamine -one of the first antifungals of the allylamine class, discovered in 1974. It was approved for systemic use in the UK in 1991, and for topical use in the USA in 1992.
Terbinafine is an antifungal effective against
Dermatophytes, Aspergillus
sp., and
Candida and Pityrosporum yeasts
. Terbinafine is only fungistatic against Candida, however cure is possible after 2-4 weeks of treatment (-).
It is available in systemic and topical formulations. Systemic treatment is usually reserved for infections of the nails, extensive cutaneous infections or those, which have not responded to topical therapy.
Trade Name:
Lamisil* Novartis
Lamisil DermGel* Novartis
Lamisil AT* Novartis
Do sage Types;
Topical: Cream:
Terbinafine hydrochloride 1% *
Lamisil* and Lamisil AT
Solution:
Terbinafine hydrochloride Lamisil
Oral: Tablets:
Terbinafine hydrochloride tablets 250 mg Lamisil*
Therapeutic Regimen
Adult
Pediatric
Oral
Onychomycosis
Lamisil 250 mg po daily x6 weeks for the fingernails, and x12 weeks for the toenails.
Tinea cruris, corporis and pedis
Lamisil 250 mg po daily x2-6 weeks
Topical
Tinea corporis and cruris
Lamisil 1% 1-2x/d x1 week until significant improvement shows.
Treatment should not be continued after 4 weeks.
Tinea pedis
Lamisil 1% 2x/d x2 weeks until significant improvement shows.
Treatment should not be continued after 4 weeks.
Tinea versicolor.
Lamisil 1% 1-2x/d x2 weeks until significant improvement shows.
Treatment should not be continued after 4 weeks.
Cutaneous candidiasis
Lamisil 1% 1-2x/d x1-2 weeks until significant improve ment shows.
Treatment should not be continued after 4 weeks.
Oral
Safety and efficacy have not been established
Topical
Safety and efficacy have not been established in children < 12 years of age
Patient Monitoring
Liver function tests are recommended before treatment and periodically during therapy, in patients with hepatic impairment, alcoholism, and those taking hepatotoxic drugs.
Adverse Effects
Local cutaneous effects may include mild burning, irritation, and erythema.
Cutaneous effects may include hypersensitivity reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis.
Gastrointestinal effects may include nausea, dyspepsia, stomach pain, reversible loss of taste and hepatitis.
Hematologic effects may include neutropenia and pancytopenia.
FDA Pregnancy Category B
Human tests have not been completed, but animal testing has not shown any adverse fetal effects. Terbinafine is distribu ted in the breast milk. Treatment during pregnancy and lactation is not recommended.
Major Drug Interactions
Concurrent use of terbinafine with caffeine, theophylline and naphtylline may increase their toxicity; alcohol and hepatotoxic medications may increase the risk of liver damage; drugs that induce the cytochrome P-450 system may increase the clearance of terbinafine; drugs that inhibit the cytochrome P-450 system may decrease the clearance of terbinafine.
Mechanism of Action / Pharmacokinetics
Terbinafine interferes with fungal ergosterol synthesis by inhibiting the enzyme squalene epoxide in the fungal cell membrane.
This leads to fungal cell death by disruption of fungal membrane function and cell wall synthesis. The oral dose is well absorbed from the gastrointestinal tract, and is extensively distributed to the hair follicle, nail plate and sebum-rich skin.
It can be detected in nail clippings three weeks after the initiation of therapy.
Ter binafine undergoes first pass metabolism, involving a small percentage of the total hepatic P450 capacity. Its elimination is primarily renal.
Topical terbinafine is minimally absorbed, less than 5% is detected systemically. Topical terbinafine concentrates in the lipophilic stratum corneum
General References
Elewski BE: Tinea capitis: A current perspective. Jour. Am. Acad. Derm. 2000: 42: 1-20
Gupta AK, Shear NH: Terbinafine: An Update. Jour. Am. Acad. Derm. 1997: 37: 979-988
Caceres-Rios H, Rueda M, Ballona R, et al: Comparison of terbinafine and Griseofulvin in the treatment of tinea capitis. Jour. Am. Acad. Derm. 2000: 42: 80-84
Evans EGV, Sigurgeirsson B, LIONS Study Group: Double blind randomised study of continuous terbinafine compared with intermittent Itraconazole in treatment of toenail onychomycosis. Br. Med. Jour. 1999: 318: 1031-1035
Krafchik B: The Clinical Efficacy of Terbinafine in the treatment of Tinea Capitis. Rev. Contemp. Pharma cother. 1997 ; 8 ; 313-324
Zaias N, Serrano L: the successful treatment of finger trichophytum rubrum onychomycosis with oral terbinafine. Clin. Exp. Derm. 1989: 14: 120-123 Gupta AK, Shear NH: A risk-benefit assessment of newer oral antifungal agents used to treat onychomycosis. Drug Safety: 2000: 22: 33-52
Gupta AK, Lynde CW, Lauzon GJ, et al: Cutaneous adverse effects associated with terbinafine therapy: 10 case reports and a review of the literature. Br. Jour. Derm. 1998: 138: 529-532
Ornstein DL, Ely P: Reversible agranulocytosis associated with oral terbinafine for onychomycosis. Jour. Am. Acad. Derm. 1998: 39 (6): 1023-1024
Shapiro M, Li L-J, Miller J: Terbinafine-induced neutropenia. Br. Jour. Derm. 1999: 140: 1169-1199
Terbinafine Hydrochloride
Antifungal, allylamine -one of the first antifungals of the allylamine class, discovered in 1974. It was approved for systemic use in the UK in 1991, and for topical use in the USA in 1992.
Terbinafine is an antifungal effective against
Dermatophytes, Aspergillus
sp., and
Candida and Pityrosporum yeasts
. Terbinafine is only fungistatic against Candida, however cure is possible after 2-4 weeks of treatment (-).
It is available in systemic and topical formulations. Systemic treatment is usually reserved for infections of the nails, extensive cutaneous infections or those, which have not responded to topical therapy.
Trade Name:
Lamisil* Novartis
Lamisil DermGel* Novartis
Lamisil AT* Novartis
Do sage Types;
Topical: Cream:
Terbinafine hydrochloride 1% *
Lamisil* and Lamisil AT
Solution:
Terbinafine hydrochloride Lamisil
Oral: Tablets:
Terbinafine hydrochloride tablets 250 mg Lamisil*
Therapeutic Regimen
Adult
Pediatric
Oral
Onychomycosis
Lamisil 250 mg po daily x6 weeks for the fingernails, and x12 weeks for the toenails.
Tinea cruris, corporis and pedis
Lamisil 250 mg po daily x2-6 weeks
Topical
Tinea corporis and cruris
Lamisil 1% 1-2x/d x1 week until significant improvement shows.
Treatment should not be continued after 4 weeks.
Tinea pedis
Lamisil 1% 2x/d x2 weeks until significant improvement shows.
Treatment should not be continued after 4 weeks.
Tinea versicolor.
Lamisil 1% 1-2x/d x2 weeks until significant improvement shows.
Treatment should not be continued after 4 weeks.
Cutaneous candidiasis
Lamisil 1% 1-2x/d x1-2 weeks until significant improve ment shows.
Treatment should not be continued after 4 weeks.
Oral
Safety and efficacy have not been established
Topical
Safety and efficacy have not been established in children < 12 years of age
Patient Monitoring
Liver function tests are recommended before treatment and periodically during therapy, in patients with hepatic impairment, alcoholism, and those taking hepatotoxic drugs.
Adverse Effects
Local cutaneous effects may include mild burning, irritation, and erythema.
Cutaneous effects may include hypersensitivity reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis.
Gastrointestinal effects may include nausea, dyspepsia, stomach pain, reversible loss of taste and hepatitis.
Hematologic effects may include neutropenia and pancytopenia.
FDA Pregnancy Category B
Human tests have not been completed, but animal testing has not shown any adverse fetal effects. Terbinafine is distribu ted in the breast milk. Treatment during pregnancy and lactation is not recommended.
Major Drug Interactions
Concurrent use of terbinafine with caffeine, theophylline and naphtylline may increase their toxicity; alcohol and hepatotoxic medications may increase the risk of liver damage; drugs that induce the cytochrome P-450 system may increase the clearance of terbinafine; drugs that inhibit the cytochrome P-450 system may decrease the clearance of terbinafine.
Mechanism of Action / Pharmacokinetics
Terbinafine interferes with fungal ergosterol synthesis by inhibiting the enzyme squalene epoxide in the fungal cell membrane.
This leads to fungal cell death by disruption of fungal membrane function and cell wall synthesis. The oral dose is well absorbed from the gastrointestinal tract, and is extensively distributed to the hair follicle, nail plate and sebum-rich skin.
It can be detected in nail clippings three weeks after the initiation of therapy.
Ter binafine undergoes first pass metabolism, involving a small percentage of the total hepatic P450 capacity. Its elimination is primarily renal.
Topical terbinafine is minimally absorbed, less than 5% is detected systemically. Topical terbinafine concentrates in the lipophilic stratum corneum
General References
Elewski BE: Tinea capitis: A current perspective. Jour. Am. Acad. Derm. 2000: 42: 1-20
Gupta AK, Shear NH: Terbinafine: An Update. Jour. Am. Acad. Derm. 1997: 37: 979-988
Caceres-Rios H, Rueda M, Ballona R, et al: Comparison of terbinafine and Griseofulvin in the treatment of tinea capitis. Jour. Am. Acad. Derm. 2000: 42: 80-84
Evans EGV, Sigurgeirsson B, LIONS Study Group: Double blind randomised study of continuous terbinafine compared with intermittent Itraconazole in treatment of toenail onychomycosis. Br. Med. Jour. 1999: 318: 1031-1035
Krafchik B: The Clinical Efficacy of Terbinafine in the treatment of Tinea Capitis. Rev. Contemp. Pharma cother. 1997 ; 8 ; 313-324
Zaias N, Serrano L: the successful treatment of finger trichophytum rubrum onychomycosis with oral terbinafine. Clin. Exp. Derm. 1989: 14: 120-123 Gupta AK, Shear NH: A risk-benefit assessment of newer oral antifungal agents used to treat onychomycosis. Drug Safety: 2000: 22: 33-52
Gupta AK, Lynde CW, Lauzon GJ, et al: Cutaneous adverse effects associated with terbinafine therapy: 10 case reports and a review of the literature. Br. Jour. Derm. 1998: 138: 529-532
Ornstein DL, Ely P: Reversible agranulocytosis associated with oral terbinafine for onychomycosis. Jour. Am. Acad. Derm. 1998: 39 (6): 1023-1024
Shapiro M, Li L-J, Miller J: Terbinafine-induced neutropenia. Br. Jour. Derm. 1999: 140: 1169-1199
Clarithromycin / CAS NO.: 81103-11-9
Clarithromycin
CAS NO.: 81103-11-9
Strong supplier of Clarithromycin from China
Product: Clarithromycin
CAS NO.: 81103-11-9
M.F.: C38H69NO13
M.W.: 747.9534
Appearance: white crystalline powder
Package: 25kg/fibre drum
Spec.: CP2005 USP26
Usage: it is a macrolide antibiotic for the treatment of upper and lower respiratory tract infections, skin and soft tissue infections
CAS NO.: 81103-11-9
Strong supplier of Clarithromycin from China
Product: Clarithromycin
CAS NO.: 81103-11-9
M.F.: C38H69NO13
M.W.: 747.9534
Appearance: white crystalline powder
Package: 25kg/fibre drum
Spec.: CP2005 USP26
Usage: it is a macrolide antibiotic for the treatment of upper and lower respiratory tract infections, skin and soft tissue infections
Menthol Crystal (Korsher & Halal certificate)
Chinese Leading Manufacturer of Menthol Crystal, 3000MT/year output, latest tech, top quality, GMP standard.
Assay(GC): >99.70
The material is widely used in pharmaceutical, food, cigarettes, toothpastes, and cosmetics.
Color and Appearance: Colorless, transparent hexagonal or needlelike crystals.
Odor: Having Characteristic odor of natural menthol obtained from mentha arvensis oil.
Standard:
Specifications
BP
USP
JP
FCC-III
GLG
Melting Point (°C)
41 to 44
41 to 44
42 to 44
42 to 44
42 to 44
Optical Rotation
-49 to -50
-49 to -50
-49 to -50
-49 to -50
-49 to -50
Non-volatile Matter
0.05%
0.05%
0.05%
0.05%
0.05%
Menthol (NLT)
Not Specified
97.00%
98.00%
Not Specified
99.70%
GLG - Green Leaf Group Menthol Crystals
USP - United States Pharmacopoeia
JP - Japanese Pharma
BP - British Pharmacopoeia
FCC-III Food Codex (American Food Grade)
Certification : ISO 9001-2008, HALAL and KOSHER
Packing solutions:
i) Menthol Crystals in Fibre Drums with Lining of Thermocol and food grade polythene bag of 25 Kgs. net.
ii) Menthol Crystals in galvanized Iron Tins with Lining of Thermocol and food grade polythene bag of 2.5 Kgs. net. 12 tins in one carton, 30kgs net each carton.
Assay(GC): >99.70
The material is widely used in pharmaceutical, food, cigarettes, toothpastes, and cosmetics.
Color and Appearance: Colorless, transparent hexagonal or needlelike crystals.
Odor: Having Characteristic odor of natural menthol obtained from mentha arvensis oil.
Standard:
Specifications
BP
USP
JP
FCC-III
GLG
Melting Point (°C)
41 to 44
41 to 44
42 to 44
42 to 44
42 to 44
Optical Rotation
-49 to -50
-49 to -50
-49 to -50
-49 to -50
-49 to -50
Non-volatile Matter
0.05%
0.05%
0.05%
0.05%
0.05%
Menthol (NLT)
Not Specified
97.00%
98.00%
Not Specified
99.70%
GLG - Green Leaf Group Menthol Crystals
USP - United States Pharmacopoeia
JP - Japanese Pharma
BP - British Pharmacopoeia
FCC-III Food Codex (American Food Grade)
Certification : ISO 9001-2008, HALAL and KOSHER
Packing solutions:
i) Menthol Crystals in Fibre Drums with Lining of Thermocol and food grade polythene bag of 25 Kgs. net.
ii) Menthol Crystals in galvanized Iron Tins with Lining of Thermocol and food grade polythene bag of 2.5 Kgs. net. 12 tins in one carton, 30kgs net each carton.
best selling piroctone olamine/Octopirox, OCTO, OCT
best selling piroctone olamine/Octopirox, OCTO, OCT
1 professional and leading manufacturer
2 Assay:min 99%
3 C14H23NO2 C2H7
best selling piroctone olamine/Octopirox, OCTO, OCT
1 professional and leading manufacturer
2 Assay:min 99%
3 C14H23NO2 C2H7
General description
Piroctone olamine
[27503-81-7]
Synonyms:
1-Hydroxy-4-methyl-6-(2,4,4-trimethypentyl)-2-pyridon and its monoethanolamine salt; P.O.
Structure:
Molecular Formula:
C14H23NO2 C2H7NO
Molecular Weight:
298.48
Appearance:
White crystal powder
Purity:
≥99.0%
Melting Point:
Package:
Cartoon Drum, 25KG Net
Should any interest in it or any other pending enquiry, pls contact me freely.And looking forward to having yo ur reply then.
Best regards
(Ms.)Joy Zhang
Xiamen Forever Green Source Biochem Tech. Co., Ltd.
Tel: 0086-592-5812532 Fax: 0086-592-5639276/5185053
ISO9001:2008
1 professional and leading manufacturer
2 Assay:min 99%
3 C14H23NO2 C2H7
best selling piroctone olamine/Octopirox, OCTO, OCT
1 professional and leading manufacturer
2 Assay:min 99%
3 C14H23NO2 C2H7
General description
Piroctone olamine
[27503-81-7]
Synonyms:
1-Hydroxy-4-methyl-6-(2,4,4-trimethypentyl)-2-pyridon and its monoethanolamine salt; P.O.
Structure:
Molecular Formula:
C14H23NO2 C2H7NO
Molecular Weight:
298.48
Appearance:
White crystal powder
Purity:
≥99.0%
Melting Point:
Package:
Cartoon Drum, 25KG Net
Should any interest in it or any other pending enquiry, pls contact me freely.And looking forward to having yo ur reply then.
Best regards
(Ms.)Joy Zhang
Xiamen Forever Green Source Biochem Tech. Co., Ltd.
Tel: 0086-592-5812532 Fax: 0086-592-5639276/5185053
ISO9001:2008
Pharmaceutical for Zoledronic acid
Product Name: Zoledronic Acid
1.Assay:99%
2.Molecular weight:290.11
3.Appearance:White crystalline powder
Classification:Pharmaceutical intermediates
Product name:Zoledronic acid
CAS No.:118072-93-8
Apperance:White or off-white crystalline powder
Indications: Treatment of bone pain
1.Assay:99%
2.Molecular weight:290.11
3.Appearance:White crystalline powder
Classification:Pharmaceutical intermediates
Product name:Zoledronic acid
CAS No.:118072-93-8
Apperance:White or off-white crystalline powder
Indications: Treatment of bone pain
Capsaicin
Capsaicin is a unique antiphlogistic long-term analgesia substances.
1, capsaicin is a Solanaceae plant pepper (Capicum frutescens L.) were spicy fruit in the main material is a very spicy vanilla amide alkaloids, with a variety of complex physiological and pharmacological activity, some containing substance P feel nervous system, cardiovascular, pulmonary function, body temperature regulation, gastrointestinal function have a significant effect, with anti-inflammatory analgesic, promote fat metabolism, such as the role of tear, the more prominent of which is its unique long-acting analgesic effect ,
2, capsaicin has been contained in a USP 24 version, widely used to treat arthritis, muscle pain, back pain, sports sprains and postherpetic neuralgia, etc. left over. By the American Medical Association (AMA) editor of "Drug Evaluasion& quot; will also be made to pay for the treatment of postherpetic neuralgia, diabetic neuropathic pain, the drug of choice. Now mainly used as topical analgesics, drug analgesic, antipruritic, Jianweixiaoshi agent, prevent heart disease drugs, diet pills, pesticides and other military applications ,
3, capsaicin, is contained in a pepper and spicy vanilla amide alkaloids. Is a high-quality dry red chili as the raw material, using modified solvent, by crushing, extraction, separation, concentration, refining, purification and get flaky or needle-like crystals. Pure capsaicin has a number of physiological activity can be anti-inflammatory analgesic, blood circulation ,
4, capsaicin is currently used topical creams to relieve such as shingles caused by post-herpetic neuralgia of peripheral neuropathy pain. It can be used between the concentration of 0.025% and 0.075%. It is used as a temporary relief from muscle pain and arthritis, back pain, sprain pain. As a local an esthetic is usually clinical, but also as a post-operative pain ,
1,
capsaicin is a Solanaceae plant pepper (Capicum frutescens L.) were spicy fruit in the main material is a very spicy vanilla amide alkaloids, with a variety of complex physiological and pharmacological activity, some containing substance P feel nervous system, cardiovascular, pulmonary function, body temperature regulation, gastrointestinal function have a significant effect, with anti-inflammatory analgesic, promote fat metabolism, such as the role of tear, the more prominent of which is its unique long-acting analgesic effect
,
2, capsaicin has been contained in a USP 24 version, widely used to treat arthritis, muscle pain, back pain, sports sprains and postherpetic neuralgia, etc. left over. By the American Medical Association (AMA) editor of "Drug Evaluasion" will also be made to pay for the treatment of postherpetic neuralgia, diabetic neuropathic pain, the drug of choice. Now mainly used as topical analgesics, drug analgesic, antipruritic, Jianweixiaoshi agent, prevent heart disease drugs, diet pills, pesticides and other military applications
,
3, capsaicin, is contained in a pepper and spicy vanilla amide alkaloids. Is a high-quality dry red chili as the raw material, using modified solvent, by crushing, extraction, separation, concentration, refining, purification and get flaky or needle-like crystals. Pure capsaicin has a number of physiological activity can be anti-inflammatory analgesic, blood circulation
,
4, capsaicin is currently used topical creams to relieve such as shingles caused by post-herpetic neuralgia of peripheral neuropathy pain. It can be used between the concentration of 0.025% and 0.075%. It is used as a temporary relief from muscle pain and arthritis, back pain, sprain pain. As a local anesthetic is usually clinical, but also as a post-operative pain
,
1, capsaicin is a Solanaceae plant pepper (Capicum frutescens L.) were spicy fruit in the main material is a very spicy vanilla amide alkaloids, with a variety of complex physiological and pharmacological activity, some containing substance P feel nervous system, cardiovascular, pulmonary function, body temperature regulation, gastrointestinal function have a significant effect, with anti-inflammatory analgesic, promote fat metabolism, such as the role of tear, the more prominent of which is its unique long-acting analgesic effect ,
2, capsaicin has been contained in a USP 24 version, widely used to treat arthritis, muscle pain, back pain, sports sprains and postherpetic neuralgia, etc. left over. By the American Medical Association (AMA) editor of "Drug Evaluasion& quot; will also be made to pay for the treatment of postherpetic neuralgia, diabetic neuropathic pain, the drug of choice. Now mainly used as topical analgesics, drug analgesic, antipruritic, Jianweixiaoshi agent, prevent heart disease drugs, diet pills, pesticides and other military applications ,
3, capsaicin, is contained in a pepper and spicy vanilla amide alkaloids. Is a high-quality dry red chili as the raw material, using modified solvent, by crushing, extraction, separation, concentration, refining, purification and get flaky or needle-like crystals. Pure capsaicin has a number of physiological activity can be anti-inflammatory analgesic, blood circulation ,
4, capsaicin is currently used topical creams to relieve such as shingles caused by post-herpetic neuralgia of peripheral neuropathy pain. It can be used between the concentration of 0.025% and 0.075%. It is used as a temporary relief from muscle pain and arthritis, back pain, sprain pain. As a local an esthetic is usually clinical, but also as a post-operative pain ,
1,
capsaicin is a Solanaceae plant pepper (Capicum frutescens L.) were spicy fruit in the main material is a very spicy vanilla amide alkaloids, with a variety of complex physiological and pharmacological activity, some containing substance P feel nervous system, cardiovascular, pulmonary function, body temperature regulation, gastrointestinal function have a significant effect, with anti-inflammatory analgesic, promote fat metabolism, such as the role of tear, the more prominent of which is its unique long-acting analgesic effect
,
2, capsaicin has been contained in a USP 24 version, widely used to treat arthritis, muscle pain, back pain, sports sprains and postherpetic neuralgia, etc. left over. By the American Medical Association (AMA) editor of "Drug Evaluasion" will also be made to pay for the treatment of postherpetic neuralgia, diabetic neuropathic pain, the drug of choice. Now mainly used as topical analgesics, drug analgesic, antipruritic, Jianweixiaoshi agent, prevent heart disease drugs, diet pills, pesticides and other military applications
,
3, capsaicin, is contained in a pepper and spicy vanilla amide alkaloids. Is a high-quality dry red chili as the raw material, using modified solvent, by crushing, extraction, separation, concentration, refining, purification and get flaky or needle-like crystals. Pure capsaicin has a number of physiological activity can be anti-inflammatory analgesic, blood circulation
,
4, capsaicin is currently used topical creams to relieve such as shingles caused by post-herpetic neuralgia of peripheral neuropathy pain. It can be used between the concentration of 0.025% and 0.075%. It is used as a temporary relief from muscle pain and arthritis, back pain, sprain pain. As a local anesthetic is usually clinical, but also as a post-operative pain
,
Peramivir
Peramivir 98%min
CAS No.229614-55-5
Best price
free sample
Chemical Name: Peramivir
CAS RN: 229614-55-5
Synonym:
3(R)-[1(S)-Acetamido-2-ethylbutyl]-4(R)-guanidino-2(S)-hydroxycyclopentane-1(S)-carboxylic acid;
Molecular Formula: C15-H28-N4-O4
Molecular Weight: 328.4102
Peramivir is a novel cyclopentane resistance of the influenza virus, is the firm and the Zanamivir wei wei Oseltamivir r&d department meters and in 1999 successfully listed after another new flu virus making inhibitors. This drug in 2000 by the Australian national university school of leadership in Babu professor developed successfully. For foreign body inside and outside of the arv wei lamy experiment and clinical trials showed that the drugs can effectively restrain the strains of influenza virus replication and propagation process, with superior tolerability, small toxicity, etc
ANTIINFECTIVE THERAPY, Anti-Influenza Virus Drugs, Antiviral Drugs, Neuraminidase (Sialidase) Inhibitors
CAS No.229614-55-5
Best price
free sample
Chemical Name: Peramivir
CAS RN: 229614-55-5
Synonym:
3(R)-[1(S)-Acetamido-2-ethylbutyl]-4(R)-guanidino-2(S)-hydroxycyclopentane-1(S)-carboxylic acid;
Molecular Formula: C15-H28-N4-O4
Molecular Weight: 328.4102
Peramivir is a novel cyclopentane resistance of the influenza virus, is the firm and the Zanamivir wei wei Oseltamivir r&d department meters and in 1999 successfully listed after another new flu virus making inhibitors. This drug in 2000 by the Australian national university school of leadership in Babu professor developed successfully. For foreign body inside and outside of the arv wei lamy experiment and clinical trials showed that the drugs can effectively restrain the strains of influenza virus replication and propagation process, with superior tolerability, small toxicity, etc
ANTIINFECTIVE THERAPY, Anti-Influenza Virus Drugs, Antiviral Drugs, Neuraminidase (Sialidase) Inhibitors
low molecular hyaluronic acid gel injection ( Source: Fermented)
cross linked hyaluronic acid gel injection
made of High purity Hyaluronic acid
molecular>1,600,000
high flexib
Filling For Cosmetic Surgery
(
Injecting Gel
)
terms of payment L/C,T/T, Western Union
Delivery 5-10 days
Product Description
Products structure
Hyaluronic acid(HA for short)is a kind of Acidic mucopolysaccharide macromolecules, it is wildly contained in the anmials and human organism, which molecule is cross bonding by the N-acetylglucosamine and D-D-glucuronic acid disaccharide unit. It shows Naturally curly linear-shaped, its Sodium salt crystals is White amorphous solid, Colorless and tasteless,it has a strong absorptionand Moisture Retention.Molecular Structure as below
Molecular formula (C
14
H
20
NO
11
Na)
n
This product is made of H igh purity Hyaluronic acid, It’s an ideal soft tissue filling agent in non-surgical plastic surgery, the everage molecular weight ≥1.6 x10
6
,and inject it into the subcutaneous by very fine needles. to fill depressions of the skin, to make the Wrinkles and creases maximum flattening. It can be used to fill cheek and build the lip shape.
This product has already got the approbationby the customers both at home and abroad, it’s a high flexible, sterile, pyrogen-freematerial, which has good rheological properties of polymeric biomaterials Polysaccharides.it is filled with the injectable agents,simple for the opearation.
Product Attribute
The high biocompatibility in the skin, subcutaneous and intramuscular; Anti-degradation; Anti-migration;Difficult to absorb;Long half-life; No inflammation after implantation; Mmune response or Foreign body reaction;it has a relative stability and biocompatibility in the soft tissue,No skin test,Fa st, safe and effective; good Moisture.
Serviceable Range
Shaping Facial Contours
Correcting Hollow Cheeks
Improving Chin
Treating Wrinkles
Treating Forehead Wrinkles
Treating Glabellar Lines
Treating Periorbital Lines
Treating Oral Commissures
Treating Nasolabial Folds
Treating Philtrum Ridges
Treating Lips
Treating Neck Lines
Specification
1.0ml/piece (2.0%HA-Na)
Advantage of
Rhytidectomy
-It can keep 10-14 months’ effects.
-It can not go into lion face.
-It’s easy to get the smooth effects after use to fill the recess on your face.
-Fast and safe treatment,scars can’t be left.
-High safety and there will be no allergic reaction.
Use Restriction
-The women who are in lactation can not be injected.
-The people who is allergic with the Pharmaceutical components.
-The people who is using the pharmaceutical of Muscle relaxant disease.
-The people who has Allergic reaction to Grant's positive bacterial proteins.
-It can not injected into blood vessel.
Side Effect
after injection, it may appear the tumidness, rubeosis, ache, ecchymoma and having a soft and loose touch in the injection site, All of the symptom above will get better in one week after injection.
Notes Before Injection
-Please do not do face-painting and drinking on the day you injected.
-If you are using Aspirin or other Anticoagulant drug, please stop using it for days before you injected, be aware that these may increase the bruising and bleeding at the injection site.
-If the package damaged,the preparation product should be discarded.
Notes After Injection
-It will a little pain in your head after several hours when you injected.
-Please don’t do face-painting and drinking on the same day after you injected.
-Please do remember that you should not knead of your face, to avoid of hyaluronic acid has not stereotyping yet.
-Strongly require that please do not touch the injected site on your face in 6hours.
-Please do not get Sunbathing, or go into the warm place, steam room, or freezing place, To avoid the damage of the filler before Combined with the skin, after injected within one week.
-Please do not use Aspirin or other Anti-inflammatory painkillers, and do not eat gingko, garlic, vitamin A, vitamin E, Essential Fatty Acid.
-Injceted after 23 weeks, if there still feel a slight lump, please don’t worry,it will get soft soon.
made of High purity Hyaluronic acid
molecular>1,600,000
high flexib
Filling For Cosmetic Surgery
(
Injecting Gel
)
terms of payment L/C,T/T, Western Union
Delivery 5-10 days
Product Description
Products structure
Hyaluronic acid(HA for short)is a kind of Acidic mucopolysaccharide macromolecules, it is wildly contained in the anmials and human organism, which molecule is cross bonding by the N-acetylglucosamine and D-D-glucuronic acid disaccharide unit. It shows Naturally curly linear-shaped, its Sodium salt crystals is White amorphous solid, Colorless and tasteless,it has a strong absorptionand Moisture Retention.Molecular Structure as below
Molecular formula (C
14
H
20
NO
11
Na)
n
This product is made of H igh purity Hyaluronic acid, It’s an ideal soft tissue filling agent in non-surgical plastic surgery, the everage molecular weight ≥1.6 x10
6
,and inject it into the subcutaneous by very fine needles. to fill depressions of the skin, to make the Wrinkles and creases maximum flattening. It can be used to fill cheek and build the lip shape.
This product has already got the approbationby the customers both at home and abroad, it’s a high flexible, sterile, pyrogen-freematerial, which has good rheological properties of polymeric biomaterials Polysaccharides.it is filled with the injectable agents,simple for the opearation.
Product Attribute
The high biocompatibility in the skin, subcutaneous and intramuscular; Anti-degradation; Anti-migration;Difficult to absorb;Long half-life; No inflammation after implantation; Mmune response or Foreign body reaction;it has a relative stability and biocompatibility in the soft tissue,No skin test,Fa st, safe and effective; good Moisture.
Serviceable Range
Shaping Facial Contours
Correcting Hollow Cheeks
Improving Chin
Treating Wrinkles
Treating Forehead Wrinkles
Treating Glabellar Lines
Treating Periorbital Lines
Treating Oral Commissures
Treating Nasolabial Folds
Treating Philtrum Ridges
Treating Lips
Treating Neck Lines
Specification
1.0ml/piece (2.0%HA-Na)
Advantage of
Rhytidectomy
-It can keep 10-14 months’ effects.
-It can not go into lion face.
-It’s easy to get the smooth effects after use to fill the recess on your face.
-Fast and safe treatment,scars can’t be left.
-High safety and there will be no allergic reaction.
Use Restriction
-The women who are in lactation can not be injected.
-The people who is allergic with the Pharmaceutical components.
-The people who is using the pharmaceutical of Muscle relaxant disease.
-The people who has Allergic reaction to Grant's positive bacterial proteins.
-It can not injected into blood vessel.
Side Effect
after injection, it may appear the tumidness, rubeosis, ache, ecchymoma and having a soft and loose touch in the injection site, All of the symptom above will get better in one week after injection.
Notes Before Injection
-Please do not do face-painting and drinking on the day you injected.
-If you are using Aspirin or other Anticoagulant drug, please stop using it for days before you injected, be aware that these may increase the bruising and bleeding at the injection site.
-If the package damaged,the preparation product should be discarded.
Notes After Injection
-It will a little pain in your head after several hours when you injected.
-Please don’t do face-painting and drinking on the same day after you injected.
-Please do remember that you should not knead of your face, to avoid of hyaluronic acid has not stereotyping yet.
-Strongly require that please do not touch the injected site on your face in 6hours.
-Please do not get Sunbathing, or go into the warm place, steam room, or freezing place, To avoid the damage of the filler before Combined with the skin, after injected within one week.
-Please do not use Aspirin or other Anti-inflammatory painkillers, and do not eat gingko, garlic, vitamin A, vitamin E, Essential Fatty Acid.
-Injceted after 23 weeks, if there still feel a slight lump, please don’t worry,it will get soft soon.
Sunday, September 4, 2011
Rifampicin
BP/USP/EP
Packaging & Delivery
Packaging Detail:
5kgs/drum; 25kgs/drum; 25kgs/carton
Delivery Detail
within 7 to 15 days
Specifications
Rifampicin (Rifampin):
1.Antibiotics for the treatment of tuberculosis
2.BP/USP/EP
Rifampicin (Rifampin):
Product name:
Rifampicin (Rifampin)
CAS No.
13292-46-1
Chemical name:
3-{[(4-Methyl-1-piperazinyl)imino]-methyl}rifamycin
Molecular formula:
C
43
H
58
N
4
O
12
Molecular weight:
822.9508
Applications:
Antibiotics for the treatment of tuberculosis.
Appearance:
A Reddish Brown to Brownish Red Crystalline powder.
Specification:
BP/USP/EP.
Bulk Density:
0.3g/ml; 0.5g/ml; 0.7g/ml; 0.8g/ml
Standard Packaging:
5kgs/drum; 25kgs/drum; 25kgs/carton
VET APIs
Antibacterials
Amoxiciline Trihydrate
Azithromycin
Antipyrine
Cefquinome Sulphate
Ceftiofur
Colistin Sulphate
Carbadox
Chlortetracycline HCL
Clindamycine HCL
Clindamycin Sulfate
Cloxacillin Sodium
Cloxacillin Benzathine
Doxycyline HCL
Danofloxacin Mesylate
Diaveridine HCL
Enrofloxacin Base
Erythromycin Thiocyanate
Florfenicol
Gentamycin Sulfate
Penicillin V Potassium
Pirlimycin
Oxytetracyline HCL
OTC Base
Linomycin HCL
Mequindox
Nifuroxazide
Neomycin Sulfate
Norfloxacin Base
Rifampicin
Roxarsone
Salinomycin
Sulfadiazine
Sulfadiazine Base
Sulfadimethoxine Sodium
Sulfadimethoxine Base
Sulfadimidine
Sulfathiazole
Sulfaguanidine
Streptomycin
Thiamphenicol
Tilmicosin base
Tilmicosin Phosphate
Trimebutine Maleate
TMP
Tylosin Tartrate
Super Tylosin
Valnemulin
Zinc Bacitracin
Metronidazole
Antiparasitics
Amprolium HCL
Buparvaquone
ClorsulonDiclazuril
Dimetridazole
Ethopabate
Maduramycin
Imidocarb dipropionate
Nicarbazine
Niclosamide
Nitroxinil
Praziquantel
Monohydrate
Sulfaquinoxaline
Totrazuril
Monesin Sodium
Vermifuges
Albendazole
Avermectin
Doramectin
Eprinomectin
Febantel
Fenbendazole
Flubendazole
Diminazene Diacenrurate
Pyrantel Pamoate
Praziquantel
Levamisole HCL
Milbemycin Oxime
Moxidectin
Oxibendazole
Oxyclozanide
Ivermectin
Rafoxanide
Fipronil
Other Medicine
Taurine
Iron Dextran Solution 10%
Amiodarone HCL
Cholesteral
Flunixin Meglumine
Ranitidine HCL
Arsanilic Acid
Bambermycin
Packaging & Delivery
Packaging Detail:
5kgs/drum; 25kgs/drum; 25kgs/carton
Delivery Detail
within 7 to 15 days
Specifications
Rifampicin (Rifampin):
1.Antibiotics for the treatment of tuberculosis
2.BP/USP/EP
Rifampicin (Rifampin):
Product name:
Rifampicin (Rifampin)
CAS No.
13292-46-1
Chemical name:
3-{[(4-Methyl-1-piperazinyl)imino]-methyl}rifamycin
Molecular formula:
C
43
H
58
N
4
O
12
Molecular weight:
822.9508
Applications:
Antibiotics for the treatment of tuberculosis.
Appearance:
A Reddish Brown to Brownish Red Crystalline powder.
Specification:
BP/USP/EP.
Bulk Density:
0.3g/ml; 0.5g/ml; 0.7g/ml; 0.8g/ml
Standard Packaging:
5kgs/drum; 25kgs/drum; 25kgs/carton
VET APIs
Antibacterials
Amoxiciline Trihydrate
Azithromycin
Antipyrine
Cefquinome Sulphate
Ceftiofur
Colistin Sulphate
Carbadox
Chlortetracycline HCL
Clindamycine HCL
Clindamycin Sulfate
Cloxacillin Sodium
Cloxacillin Benzathine
Doxycyline HCL
Danofloxacin Mesylate
Diaveridine HCL
Enrofloxacin Base
Erythromycin Thiocyanate
Florfenicol
Gentamycin Sulfate
Penicillin V Potassium
Pirlimycin
Oxytetracyline HCL
OTC Base
Linomycin HCL
Mequindox
Nifuroxazide
Neomycin Sulfate
Norfloxacin Base
Rifampicin
Roxarsone
Salinomycin
Sulfadiazine
Sulfadiazine Base
Sulfadimethoxine Sodium
Sulfadimethoxine Base
Sulfadimidine
Sulfathiazole
Sulfaguanidine
Streptomycin
Thiamphenicol
Tilmicosin base
Tilmicosin Phosphate
Trimebutine Maleate
TMP
Tylosin Tartrate
Super Tylosin
Valnemulin
Zinc Bacitracin
Metronidazole
Antiparasitics
Amprolium HCL
Buparvaquone
ClorsulonDiclazuril
Dimetridazole
Ethopabate
Maduramycin
Imidocarb dipropionate
Nicarbazine
Niclosamide
Nitroxinil
Praziquantel
Monohydrate
Sulfaquinoxaline
Totrazuril
Monesin Sodium
Vermifuges
Albendazole
Avermectin
Doramectin
Eprinomectin
Febantel
Fenbendazole
Flubendazole
Diminazene Diacenrurate
Pyrantel Pamoate
Praziquantel
Levamisole HCL
Milbemycin Oxime
Moxidectin
Oxibendazole
Oxyclozanide
Ivermectin
Rafoxanide
Fipronil
Other Medicine
Taurine
Iron Dextran Solution 10%
Amiodarone HCL
Cholesteral
Flunixin Meglumine
Ranitidine HCL
Arsanilic Acid
Bambermycin
Cefuroxime sodium
assay: detailed pls see COA or as per your required
package:1kg,5kg,10kg or per your requirement
assay: detailed pls see COA or as per your required
package:1kg,5kg,10kg or per your requirement
package:1kg,5kg,10kg or per your requirement
assay: detailed pls see COA or as per your required
package:1kg,5kg,10kg or per your requirement
enoxaparin sodium
Supplying HA
medicine, cosmetic and food grade , filler,
Source: Fermented
molecular weight(Dal): (0.3-2.8)x1,000,000
Hyaluronic acid
supply ability:20 Metric Ton per year
terms of payment: L/C,T/T, Western Union
Delivery: Promptly
Detailed product information
Product name: sodium Hyaluronate powder
CAS NO: 9067-32-7
Other name: Hyaluronic acid sodium salt; Chlamyhyaluronic acid sodium salt
Molecular: (C14H20NO11Na)n
Characters: White or almost white powder. without odor, soluble in water, unsoluble in ethabol,acetone
and aether
Package: 1kg/bag,5,10kg/drum
Cosmetic Grade:
Appearance: white powder
glucuronic acid:44% min
molecular weight(Dal): (1.0-1.5)x1,000,000
assay: 95.0% min
protein:<0.1%
residue on lgnition:20% min
pH(0.1% water solution):6.0-7.5
heavy metal(as Pb): <10ug/g
Arsenic:<2ug/g
haemolysis:Negative
Haemolytic streptococcus: negative
total bacterica:<10 CFU/g
medicine, cosmetic and food grade , filler,
Source: Fermented
molecular weight(Dal): (0.3-2.8)x1,000,000
Hyaluronic acid
supply ability:20 Metric Ton per year
terms of payment: L/C,T/T, Western Union
Delivery: Promptly
Detailed product information
Product name: sodium Hyaluronate powder
CAS NO: 9067-32-7
Other name: Hyaluronic acid sodium salt; Chlamyhyaluronic acid sodium salt
Molecular: (C14H20NO11Na)n
Characters: White or almost white powder. without odor, soluble in water, unsoluble in ethabol,acetone
and aether
Package: 1kg/bag,5,10kg/drum
Cosmetic Grade:
Appearance: white powder
glucuronic acid:44% min
molecular weight(Dal): (1.0-1.5)x1,000,000
assay: 95.0% min
protein:<0.1%
residue on lgnition:20% min
pH(0.1% water solution):6.0-7.5
heavy metal(as Pb): <10ug/g
Arsenic:<2ug/g
haemolysis:Negative
Haemolytic streptococcus: negative
total bacterica:<10 CFU/g
Methyl Salicylate BP93
BP98/USP24/26
Appearance:Colourless liquid
Content: 99.0-100.5%
CAS NO.
119-36-8
Chemical formula
Molecular Formula
C
8
H
8
O
3
Chemical Name
methyl o-Hydroxybenzoate
Other Name
Winter Green Oil
Description
Colourless or light yellow oily liquid, Melting Point-8.6°C,boiling point 223.6°C, relative density 1.1738, refractive index 1.5369, easily soluble in alcohol, acetic acid, soluble in ether, chloroform, slightly soluble in water.
Standard
BP98/USP24/26
Appearance:Colourless liquid
Content: 99.0-100.5%
Acidity:ml[0.1mol/LNaOH]/5.0g≤0.4
Relative Density:1.180-1.186
Refractive index:1.535-1.538
Heavy metals:≤0.002%(20PPm)
Solubility:2ml product can entirely dissolve in 10ml alcohol (96%)
Uses
Intermediates of medicine. Also can b e used as solvent and intermediate, widly used to manufacture insecticide, perfume, coating, cosmetics, printing ink, etc.
Packing
in 25kg grey polyethylene plastic drum or in 200kgs, 220kgs, 230kgs iron drum with plastic liner.
Storage
Stored at the place where is dry and cool. Kept in a wellclosed container. Keep away from sunlight.
Appearance:Colourless liquid
Content: 99.0-100.5%
CAS NO.
119-36-8
Chemical formula
Molecular Formula
C
8
H
8
O
3
Chemical Name
methyl o-Hydroxybenzoate
Other Name
Winter Green Oil
Description
Colourless or light yellow oily liquid, Melting Point-8.6°C,boiling point 223.6°C, relative density 1.1738, refractive index 1.5369, easily soluble in alcohol, acetic acid, soluble in ether, chloroform, slightly soluble in water.
Standard
BP98/USP24/26
Appearance:Colourless liquid
Content: 99.0-100.5%
Acidity:ml[0.1mol/LNaOH]/5.0g≤0.4
Relative Density:1.180-1.186
Refractive index:1.535-1.538
Heavy metals:≤0.002%(20PPm)
Solubility:2ml product can entirely dissolve in 10ml alcohol (96%)
Uses
Intermediates of medicine. Also can b e used as solvent and intermediate, widly used to manufacture insecticide, perfume, coating, cosmetics, printing ink, etc.
Packing
in 25kg grey polyethylene plastic drum or in 200kgs, 220kgs, 230kgs iron drum with plastic liner.
Storage
Stored at the place where is dry and cool. Kept in a wellclosed container. Keep away from sunlight.
6-Fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride
CAS:58113-30-7
NAME:4-(3-chloropropoxy)-3-methoxyacetophenone
Assay:98% white powder
use:the intermediate of Iloperidone
CAS:58113-30-7
NAME:4-(3-chloropropoxy)-3-methoxyacetophenone
Assay:98% white powder
use:the intermediate of Iloperidone
NAME:4-(3-chloropropoxy)-3-methoxyacetophenone
Assay:98% white powder
use:the intermediate of Iloperidone
CAS:58113-30-7
NAME:4-(3-chloropropoxy)-3-methoxyacetophenone
Assay:98% white powder
use:the intermediate of Iloperidone
Pharmaceutical Intermediates for Risperidone
Product Name: Risperidone
1.Assay:99%
2.Molecular weight:410.49
3.Appearance:White crystalline powder
Classification:Pharmaceutical intermediates
Product name:Risperidone
CAS No.:106266-06-2
Apperance:White or off-white crystalline powder
Mp:170°c
Indications: Anti-psychiatric disorders
1.Assay:99%
2.Molecular weight:410.49
3.Appearance:White crystalline powder
Classification:Pharmaceutical intermediates
Product name:Risperidone
CAS No.:106266-06-2
Apperance:White or off-white crystalline powder
Mp:170°c
Indications: Anti-psychiatric disorders
Terbinafine Hydrochloride
Product: Terbinafine Hydrochloride
CAS No: 78628-80-5
Molecular Formula: C21H25N
Molecular Weight: 291.4299
CAS No: 78628-80-5
Molecular Formula: C21H25N
Molecular Weight: 291.4299
restylane
Hyaluronic acid 1.0ml and 0.5ml injections contain 20 mg/ml stabilized hyaluronic acid
Hyaluronic acid 1.0ml and 0.5ml injections contain 20 mg/ml stabilized hyaluronic acid. There are approximately 100,000 gel particles per ml, and this product is to be injected in the middle part of the dermis with the enclosed 30 gauge needle. This product is recommended for glabellar wrinkles and oral commissures. It can also be used for the lips to enhance fullness, pouting and vermilion border. Hyaluronic acid 0.5ml injections contain 20 mg/ml stabilized hyaluronic acid. There are approximately 500,000 gel particles per ml, and this product is to be injected in the upper part of the dermis with the enclosed 30 gauge needle. This product is recommended for worry lines, and other thin superficial lines.
Hyaluronic acid 1.0ml and 0.5ml injections contain 20 mg/ml stabilized hyaluronic acid. There are approximately 100,000 gel particles per ml, and this product is to be injected in the middle part of the dermis with the enclosed 30 gauge needle. This product is recommended for glabellar wrinkles and oral commissures. It can also be used for the lips to enhance fullness, pouting and vermilion border. Hyaluronic acid 0.5ml injections contain 20 mg/ml stabilized hyaluronic acid. There are approximately 500,000 gel particles per ml, and this product is to be injected in the upper part of the dermis with the enclosed 30 gauge needle. This product is recommended for worry lines, and other thin superficial lines.
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