Chromium Chloride Pure & Chromic Chloride Hexahydrate USP Manufacturers CrCl2.6H2O |
Muby chemicals, is the flagship company in Mubychem Group, established in 1976, It has several manufacturing units in its wings, making Inorganic Chemicals including Chromium Chloride or Chromic Chloride Hexahydrate, Pharmaceutical Excipients & Flavour Chemicals in India.Mubychem Group has manufacturing facilities spread across Western India and sales purchase agents in several countries. The associated manufacturing units are accredited with certifications like FDA cGMP and GLP Approval, ISO-9001 ISO-14001, ISO/IEC 17025, ISO-22000, FSSC 22000, ISO 45001, Certification, "REACH" registration, Kosher, Halal & HACCP Certification. |
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CAS Number hexahydrate 10060-12-5 and anhydrous 10025-73-7.
Please visit SDS, Safety Data Sheet of Chromium Chloride or Chromic Chloride Manufacturers.
Chromic Chloride or Chromium Chloride contains not less than 98.0 percent and not more than 101.0 percent of CrCl3-6H2O.
Insoluble matter—0.01%).
Substances not precipitated by ammonium hydroxide— (0.20% as sulfate).
Sulfate— (0.01%).
Iron— The limit is 0.01%.
Chromic Chloride USP Grade Specifications - Chromium Chloride
CrCl3-6H2O --- 266.45
Chromium chloride (CrCl3) hexahydrate.
Chromium(3+) chloride hexahydrate CAS 10060-12-5
Anhydrous 158.36 CAS 10025-73-7
Chromium Chloride - Chromic Chloride or Chromium Chloride contains not less than 98.0 percent and not more than 101.0 percent of CrCl3-6H2O.
Insoluble matter— Transfer 10 g to a 250-mL beaker, add 100 mL of water, cover the beaker, and heat to boiling. Digest the hot solution on a steam bath for 30 minutes, and filter through a tarred filtering crucible of fine porosity. Rinse the beaker with hot water, passing the rinsing through the filter, and wash the filter with hot water until the last washing is colorless. Dry the filter at 105C the weight of the residue does not exceed 1 mg (0.01%).
Substances not precipitated by ammonium hydroxide— Dissolve 2.0 g of Chromic Chloride or Chromium Chloride in 80 mL of water, heat the solution to boiling, and add a slight excess of ammonium hydroxide. Continue heating to remove the excess ammonia, cool, dilute with water to 100.0 mL, and mix. Pass through a retentive filter, and transfer 50.0 mL of the clear filtrate to an evaporating dish that previously has been ignited and tarred. Add 0.5 mL of sulfuric acid to the filtrate, evaporate on a steam bath to dryness, heat gently to remove the excess acid, and ignite gently: the weight of the residue does not exceed 2.0 mg (0.20% as sulfate).
Sulfate— Prepare a test solution by dissolving 2.0 g in 10 mL of water. Add 1 mL of 3 N hydrochloric acid, filter if necessary to obtain a clear solution, wash the filter with two 5-mL portions of water, and dilute with water to 40 mL. Prepare a control solution in a similar manner, but use 1.0 g of the substance under test, and after the filtration step add 0.10 mL of 0.020 N sulfuric acid. To each solution add 3 mL of barium chloride TS, mix, and allow to stand overnight. Decant most of the supernatants, without disturbing the precipitates, but leaving twice the volume of liquid in the control solution as in the test solution. Dilute each solution with water to 25 mL, and sonicate for 1 minute: any turbidity in the test solution does not exceed that in the control solution (0.01%).
Iron— Dissolve 1.0 g of Chromic Chloride or Chromium Chloride in 100 mL of water, and mix. Transfer 10 mL of this solution to a 100-mL color comparison tube, dilute with water to 45 mL, add 2 mL of hydrochloric acid, and mix (Test Preparation). Proceed as directed for Procedure, except to add 15 mL of butyl alcohol to the Test Preparation and the Standard Preparation at the same time that the Ammonium Thiocyanate Solution is added. Shake for 30 seconds, and allow the layers to separate: the color in the upper butyl alcohol layer from the Test Preparation is not darker than that from the Standard Preparation. The limit is 0.01%.
Assay— Dissolve about 0.4 g of Chromic Chloride or Chromium Chloride, accurately weighed, in 100 mL of water contained in a glass-stoppered, 500-mL conical flask, add 5 mL of 5 N sodium hydroxide, and mix. Pipette, slowly, 4 mL of 30 percent hydrogen peroxide into the flask, and boil the solution for 5 minutes. Cool the solution slightly, and add 5 mL of nickel sulfate solution (1 in 20). Boil the solution until no more oxygen is evolved, cool, and add 2 N sulfuric acid drop wise until the color of the solution changes from yellow to orange. Add to the flask a freshly prepared solution of 4 g of potassium iodide and 2 g of sodium bicarbonate in 100 mL of water, then add 6 mL of hydrochloric acid. Immediately insert the stopper in the flask, and allow to stand in the dark for 10 minutes. Rinse the stopper and the sides of the flask with a few mL of water, and titrate the liberated iodine with 0.1 N sodium thiosulfate VS to an orange color. Add 3 mL of starch TS, and continue the titration to a blue-green endpoint. Each mL of 0.1 N sodium thiosulfate is equivalent to 8.882 mg of CrCl3·6H2O.
Chromic Chloride Anhydrous and Hexahydrate
Chromium Chloride Pure & Chromic Chloride Hexahydrate USP Manufacturers at:
Muby Chemicals & Associated Cos
BANDEALI BUILDING, CHINCHBUNDER, MUMBAI 400009, INDIA.
TEL: 91-22-23728264. Gujarat & Mumbai India.
info(At the Rate i.e. @)mubychem(dot)com
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Last updated
31-aug-22
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