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SMAART PHARMACEUTTICALS was founded by a Young Technocrat Mr. Nitten Gavande, a Chemical Engineer & Business Management Graduate, with a steadfast belief that research-based pharmaceutical industry would be the driving force behind innovations in modern healthcare. SMAART PHARMACEUTTICALS manufacturing facility is located at Jalgaon, 400km north of Mumbai, the Economic capital of INDIA & is situated 50km away from the ancient Buddhist cave temples of Ajanta. which were excavated between the 2d century BC and the 5th century AD. This state-of-the-art facility specializes in the manufacture of API's (Active Pharmaceutical Ingredients) ranging from Disinfectants to Cardiovasculars. This facility has Glass Lined Reactors, S.S Reactors, S.S centrifuges, Dryers and varied production equipment. The facilities are versatile and are capable of carrying out varied reactions ranging from -20°c to +150°c. SMAART has the capability to handle highly complex and hazardous reactions with utmost safety and productivity. SMAART’s operations are backed by a full spectrum of utilities, sophisticated quality control equipment and a 'zero discharge' environment-friendly effluent treatment plant. SMAART PHARMACEUTTICALS has established a Trading division to source world class API’s at competitive rates, directly from leading manufacturers in India and providing consistent quality and time bound shipment schedules. This has given us an additional advantage in terms of better understanding of the overseas API market & has offered more exposure in the world market
SMAART PHARMACEUTTICALS
 

CHLORHEXIDINE ACETATE BP / EP
Post date:2008-04-24

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CHLORHEXIDINE ACETATE BP / EP Tests Specifications 1 Appearance A White or almost White Crystalline Powder. Sparingly soluble in water Soluble in Alcohol, very slightly souble in glycerol and in propylene glycol. 2 Solubility Sparingly soluble in water and in propylene glycol, very slightly soluble in alcohol. 3 Identification First Identification : A, B Second Identification : B, C, D 4 Related substances Complies with B.P / E.P. test 5 Loss on drying Not More Than 3.5 % Detemined on 1.0 g by drying in an oven at 100 C TO 105 C 6 Assay on Dry Basis Chlorhexidine Acetate contains not less than 98% and not more than 101.0% of 1,1’ Hexamethylenenbis [5-(4-Chlorophenyl)-Biguanide] Diacetate, Calcculated with reference to the dired substance. 7 Sulphated Ash Not more than0.15%, determined on 1.0 g 8 4-Chloro Aniline Complies with B.P / E.P. test

Place of origin:N/A
Brand Name:N/A
Price information:N/A
Minimum order:N/A
Certification:fda approud cgmp certified
Packing information:50 kg fiber dram

 
Member since: 2005-09-06
Country: India
 Contact details:
Tel: 91 257 3296354
Fax: 91 257 2270141
Website: http://www.smaartpharma.com
Address: B-23, M.I.D.C., AJANTHA ROAD,, JALGAON, MAHARASHTRA - India
425003
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CETRIMIDE POWDER I. P . / B. P Tests Specifications 1 DESCRIPTION A White or almost white, voluminous, free-flowing powder, freely soluble in water & in alcohol. 2 IDENTIFICATION {A,B,C,D,E } TO COMPLY THE TEST 3 SOLUBILITY FREELY SOLUBLE IN WATER, IN ETHANOL {95%}, & IN CHLOROFORM. PRACTICALLY INSOLUBLE IN ETHER 4 ACIDITY OR ALKALINITY NMT. 0.1ML SOLUTION REQUIRED. 5 CLARITY & COLOUR OF SOLUTION 2.0% W/V SOLUTION IS CLEAR & COLOURLESS 6 AMINE SALTS TO COMPLY THE TEST 7 SULPHATED ASH NMT 0.5% 8 LOSS ON DRYING NMT 2% 9 ASSAY{ON D.B} BETWEEN 96% TO 101%
CETRIMIDE POWDER I. P . / B. P		 BENZALKONIUM CHLORIDE 50% SOLUTION Tests Specifications 1 DESCRIPTION A Clear,colorless liquid or slightly yellowish liquid miscible with water & with alcohol. 2 pH (10% aqueous solution) 6.5 – 7.5 3 Free Amines Nil 4 Assay 49 – 51% w/v 5 Solubility As Per BP 6 Identification As Per I P / B P 7 Acidity Or Alkalinity NMT 0.1 ml of 0.1m hydrochloric acid or 0.1m sodium hydroxide is required. 8 Appearance Of Solution As Per IP / BP. 9 Amine & Amine Salts As Per BP 10 Sulphated Ash NMT 0.1%
BENZALKONIUM CHLORIDE 50% SOLUTION		 CHLORHEXIDINE GLUCONATE 20% SOLN. IP / BP / EP / USP Tests Specifications 1 Physical Appearance Almost colorless or pale yellow liquid, miscible with water, soluble in acetone & in alcohol 2 Identification First Identification : A, B Second Identification : B, C, D. 3 pH Dilute 5.0 ml to 100.0 ml with carbon dioxide free water R. The pH of the solution is 5.5 to 7.0 4 Assay Chlorhexidine Digluconate Solution is an aqueous solution which contains not less than 190 G/L and not more than 210 G/L of 1,1’Hexamethylenenebis[5-(4-Chlorophenyl)-Biguanide]di(D Digluconate).(19-21 % w/v ) 5 Chloroaniline To comply with EP 5 / BP Test 2004 / USP 28 6 Related Substances To comply with EP 5 / BP Test 2004 / USP 28 7 Relative density 1.06 – 1.07
CHLORHEXIDINE GLUCONATE 20% SOLN. IP / BP / EP / USP		 CHLORHEXIDINE ACETATE BP / EP Tests Specifications 1 Appearance A White or almost White Crystalline Powder. Sparingly soluble in water Soluble in Alcohol, very slightly souble in glycerol and in propylene glycol. 2 Solubility Sparingly soluble in water and in propylene glycol, very slightly soluble in alcohol. 3 Identification First Identification : A, B Second Identification : B, C, D 4 Related substances Complies with B.P / E.P. test 5 Loss on drying Not More Than 3.5 % Detemined on 1.0 g by drying in an oven at 100 C TO 105 C 6 Assay on Dry Basis Chlorhexidine Acetate contains not less than 98% and not more than 101.0% of 1,1’ Hexamethylenenbis [5-(4-Chlorophenyl)-Biguanide] Diacetate, Calcculated with reference to the dired substance. 7 Sulphated Ash Not more than0.15%, determined on 1.0 g 8 4-Chloro Aniline Complies with B.P / E.P. test
CHLORHEXIDINE ACETATE BP / EP
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  CHLORHEXIDINE ACETATE BP / EP Tests Specifications 1 Appearance A White or almost White Crystalline Powder. Sparingly soluble in water Soluble in Alcohol, very slightly souble in glycerol and in propylene glycol. 2 Solubility Sparingly soluble in water and in propylene glycol, very slightly soluble in alcohol. 3 Identification First Identification : A, B Second Identification : B, C, D 4 Related substances Complies with B.P / E.P. test 5 Loss on drying Not More Than 3.5 % Detemined on 1.0 g by drying in an oven at 100 C TO 105 C 6 Assay on Dry Basis Chlorhexidine Acetate contains not less than 98% and not more than 101.0% of 1,1’ Hexamethylenenbis [5-(4-Chlorophenyl)-Biguanide] Diacetate, Calcculated with reference to the dired substance. 7 Sulphated Ash Not more than0.15%, determined on 1.0 g 8 4-Chloro Aniline Complies with B.P / E.P. test  
     
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