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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 HYDROCHLORIDE. B. P
Post date:2008-04-24
Expiry date:2008-10-09

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

Price information:N/A
Packing information:50 kg fiber dram
Quantity:N/A

 
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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BENZALKONIUM CHLORIDE 80% SOLUTION Tests Specifications 1 Description Clear transparent viscous liquid with characteristic aromatic odor 2 Solubility Soluble in water & alcohol. 3 PH(10% solution) 6.5 - 7.5 4 Free Amine Nil 5 Assay 79.0 – 81.0 w/v 6 Acidity Or Alkalinity Neutral 7 Clarity & Color Of Solution Trnsparent, Colorless 8 Sulphated Ash NMT 0.1%
BENZALKONIUM CHLORIDE 80% SOLUTION		 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		 FOSINOPRIL SODIUM U.S.P Tests Specifications 1 Description A white to off white crystalline powder. 2 Solubility Soluble in water & in methanol. 3 Identification Complies {IR,Sodium} 4 Loss on Drying 0.1% w/w { NMT 0.5 %} 5 Specific Optical Rotation {0.1% sol. In Chloroform} 4.90 { -4.50 to -6.00 on anhydrous basis} 6 Related substance { TLC } Complies { NMT 0.15 % } 7 Related substance { GC } Complies { NMT 0.15 % } 8 Related substance {HPLC} 0.10% {Fosinoprilat NMT 0.5%} 0.05% {Any Unidentified Impurity NMT 0.10%} 0.24% {Total Impurities NMT 1.0%} 9 Heavy metals Complies {NMT 20 ppm} 10 Assay { on dry basis } 100.2% { Sd be between 98.5 to 101.50% w/w } * No potential for the class-1 solvents as specified by ICH or < 467 > USP to be present in Fosinopril sodium as they are not used in the manufacturing process. The material if tested for these solvents, will comply with the established standards.
FOSINOPRIL SODIUM U.S.P		 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
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