Muby Chemicals and a few more manufacturing units are owned by Kamdar Family. Mubychem Group is the pioneer manufacturer of Gentian Violet or Methylrosanilinium Chloride etc. in India. Established in 1976, we have led a quality revolution across our product range. Mubychem group has several manufacturing facilities spread across Western India. Our associated facility is Food & Drug Administration (FDA) GMP approved to manufacture a wide range of pharmaceutical excipients and food chemicals. We have ISO-9001-2008 Certification ISO-22000-2005 HACCP Certification, Kosher and Halal Certification. We have European "Reach" Registration for exports.
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Gentian Violet USP, Gentian Violet Methylrosanilinium Chloride Manufacturers
MSDS of Gentian Violet USP & Pure Methylrosanilinium Chloride Manufacturers
Gentian Violet USP
C. I. Basic violet 3.
[4-[Bis[p-(dimethylamino)phenyl]methylene]-2,5-cyclohexadien-1-ylidene]dimethylammonium chloride [548-62-9].
Gentian Violet USP contains not less than 96.0 percent and not more than 100.5 percent of gentian violet (C25H30ClN3), calculated on the anhydrous basis.
Residue on ignition: not more than 1.5%.
Alcohol-insoluble substances— Boil 1.0 g, accurately weighed, with 50 mL of alcohol under a reflux condenser for 15 minutes, filter through a tarred filtering crucible, wash the residue on the filter with hot alcohol until the last washing is not colored violet, and dry the crucible at 105 for 1 hour: not more than 1.0% of insoluble residue remains.
Arsenic— The limit is 0.001%.
Lead— The limit is 0.003%.
Zinc standard stock solution— Transfer about 1 g of zinc, accurately weighed, to a 1000-mL volumetric flask, add 50 mL of nitric acid, and mix to dissolve. Dilute with water to volume, and mix.
Standard preparation— Dilute the Zinc standard stock solution with water to obtain a Standard preparation containing 0.50 Ag of zinc per mL.
Test preparation— Weigh accurately 0.50 g of material in a suitable tarred crucible. Place in a low-temperature plasma ashing apparatus, and ash until a constant weight is attained. Pipette 10 mL of 6 N nitric acid into the crucible, and heat to dissolve the ash. Transfer the solution to a 500-mL volumetric flask, dilute with water to volume, and mix. Prepare a reagent blank.
Procedure— Concomitantly determine the absorbance of the Standard preparation, the Test preparation, and the reagent blank at the zinc emission line at 213.9 nm, with a suitable atomic absorption spectrophotometer (see Spectrophotometry and Light-Scattering 851 ) equipped with a zinc lamp and an air–acetylene flame, using water as the blank. The absorbance of the Test preparation, corrected for that of the reagent blank, is not greater than the absorbance of the Standard preparation, similarly corrected (0.05%).
Chromatographic purity— Dissolve 10 mg in 10 mL of methanol to obtain the Test solution. Transfer 1.0 mL of Test solution to a 100-mL volumetric flask, dilute with methanol to volume, and mix (Diluted test solution). Apply 5 AL each of the Test solution and the Diluted test solution to a suitable thin-layer chromatographic plate (see Chromatography 621 ) coated with a 0.25-mm layer of octadecylsilanized chromatographic silica gel. Allow the spots to dry, and develop the chromatogram in a suitable chromatographic chamber with a solvent system consisting of the upper layer separated from a well-shaken mixture of water, butyl alcohol, and glacial acetic acid (100:80:20), until the solvent front has moved about three-fourths of the length of the plate. Remove the plate from the chamber, allow the solvent to evaporate, and visually locate the spots on the plate: the Test solution exhibits a principal spot and not more than one secondary spot which, if present in the chromatogram from the Test solution, is not more intense than the principal spot obtained from the Diluted test solution (1.0%).
Assay— Transfer about 400 mg of material, accurately weighed, to a 300-mL conical flask, add 25 mL of water and 10 mL of hydrochloric acid, displace the air in the flask with carbon dioxide, and pass a stream of carbon dioxide through the flask during the assay. Add 50.0 mL of 0.1 N titanium trichloride VS, heat to boiling, and boil gently for 10 minutes, swirling the liquid occasionally. Cool the solution, add 5 mL of ammonium thiocyanate solution (1 in 10), and titrate with 0.1 N ferric ammonium sulfate VS until a faint red color is produced. Perform a blank determination (see Residual Titrations 541 ). Each mL of 0.1 N titanium trichloride is equivalent to 20.40 mg of C25H30ClN3.
Gentian Violet is also called Crystal Violet or Basic Violet #3, Methylrosanilinium Chloride that’s the name in BP, Ph. Eur. and Hexamethyl-p-Rosaniline Chloride. IUPAC Name is 4-[(4-dimethylaminophenyl)-phenyl-methyl]-N,N-dimethyl-aniline
Gentian Violet USP from
Methylrosanilinium Chloride, Gentian Violet Manufacturers:
S-8, SARIFA MANSION, 2ND FLANK ROAD, CHINCHBUNDER, MUMBAI 400009, INDIA
TEL: (OFFICE) 91-22-23770100, 23774610, 23726950, 23723564. FAX: 91-22-23728264
USA & Canadian Customers may e-mail: firstname.lastname@example.org
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Last updated: 03 June, 2014.
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