|
|
Mubychem Group, established in
1976, is the pioneer manufacturer of Zinc Chloride, Ammonium
Chloride, Calcium Chloride, Potassium Chloride, Sodium Acetate,
Sodium Thiosulphate, Pharmaceutical, Fragrance & Flavor chemicals in
|
|
|
Email this Chromic Chloride; Chromium Chloride Page info to a Colleague or Yourself |
||
Chromic Chloride USP Chromium Chloride
Chromic Chloride - 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 Manufacturer or
Chromic Chloride Manufacturer at:
MUBY CHEMICALS
S-8, SARIFA MANSION, 2ND FLANK ROAD,
CHINCHBUNDER, MUMBAI 400009, INDIA.
TEL: (OFFICE) 91-22-23770100, 23726950,
23774610, 23723564. FAX: 91-22-23728264.
e-mail:
info@mubychem.com
Cell Call to Anmol: +91-9821870100 or Ambrish: +91-9821570100
Copyright and Usual Disclaimer is
Applicable.
Last updated
06 May, 2010
Wise men never sit and cry over their loss. But work on to redress the same.
|
Old Spice: Manufacturing since more than Three Decades: |
|||
|
Pharmaceuticals & Food Grade, IP BP USP FCC ACS A.R Gr. of Chemicals mfd. by Anmol Chemicals: |
|||
|
Chromic Chloride |
|||
Refresh Yourself with these pleasant thoughts.
I shall pass through this world, but once. If therefore, there is any good that I can do, or if there is any favour that I can show to a fellow human being, let me do it now. Let me not defer or neglect it. For I shall not tread this way again.
IT IS NICE TO BE IMPORTANT BUT ….... BUT IT IS MORE IMPORTANT TO BE NICE
If I give you “My Word” Nobody can undo it. If I sign an “Agreement” my Lawyer will undo it
