Chromium Chloride Chromic Chloride Pure & USP Manufacturers, CrCl3 |
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Chromium Chromic Chloride Manufacturers
Chromium Chloride Chromic Chloride USP
Manufacturers
MSDS of Chromium Chloride Chromic Chloride USP Manufacturers
Chromic Chloride
Technical & Pure Crystals, Chromic Chloride Hexahydrate
Also USP ACS AR LR Grades
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%.
Specifications of Chromic Chloride USP Chromium Chloride
CrCl3-6H2O
266.45
Chromium chloride (CrCl3) hexahydrate
Chromium(3+) chloride hexahydrate [10060-12-5]
Anhydrous 158.36 [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
Identification:
A: To 5 mL of a solution (1 in 250) in a test tube add 1 mL of 5 N sodium
hydroxide and 10 drops of 30 percent hydrogen peroxide, and heat gently for
about 2 minutes: a yellow color develops.
B: To 5 mL of a solution (1 in 250) in a test tube add 5 drops of silver
nitrate TS: a white, curd like precipitate is formed, and it is insoluble in
nitric acid.
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 105oC 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.
Chromium Chloride Chromic Chloride USP Manufacturers
Muby Chem Ltd.
Toll manufacturing & Warehouse at Houston & Midland, Texas, USA and India
USA, Canada, Mexico Customers may e-mail: usa@mubygroup.com
Call 1-844-682-9243
Europe Africa Asia India Mumbai e-mail: info@mubygroup.com
Call +91-22-23774610
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