Chromium Picolinate, Chromium Chloride, Chromic Chloride USP Suppliers

Teappcm, is the several decades old manufacturer supplier exporter of High Purity Chemicals including Pharmaceutical Grade Excepients like IP BP JP USP Ph Eur FCC Food Grade ACS Reagent Grade of Chemicals in India USA UAE etc. It has several associated manufacturing facilities spread across the globe. Order quantities ranging from grams, killograms to container loads are given equal attention. The participating units have one or more of the certifications like Good Manufacturing Practice, Good Laboratory Practice, ISO-9001, ISO-22000, Halal & Kosher Cettification. We also have "REACH" Preregistration.

Chromium Picolinate, Chromium Chloride, Chromic Chloride Pure & USP Grade Suppliers Exporters

Specifications of Chromium Chloride or Chromic 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: 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 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%.

Chromium Picolinate USP Grade
C18H12N3O6Cr -- 418.31
Chromium Tripicolinate.
Chromium Picolinate contains not less than 98.0 percent and not more than 102.0 percent of C18H12N3O6Cr, calculated on the dried basis.

Identification:
A: Infrared Absorption.
B: 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% hydrogen peroxide, and heat gently for about 2 minutes: a yellow color develops.
Loss on drying: Dry it at 105C for 4 hours: it loses not more than 4.0% of its weight.
Chloride: Dissolve 30 mg of Chromium Picolinate in 30 to 40 mL of water, and heat to 70C. Cool overnight, and filter to remove the precipitate. Add 1 mL each of nitric acid and silver nitrate TS, and add sufficient water to make 50 mL. Mix, and allow to stand for 5 minutes, protected from direct sunlight: any turbidity formed is not greater than that produced in a similarly treated control solution containing 0.25 mL of 0.002 N hydrochloric acid (0.06%).
Sulfate: Dissolve 100 mg of Chromium Picolinate in 30 to 40 mL of water, and heat to 90C. Cool overnight, and filter to remove the precipitate. Add 1 mL of 3 N hydrochloric acid, 3 mL of barium chloride, and sufficient water to make 50 mL. Mix, and allow to stand for 10 minutes: any turbidity formed is not greater than that produced in a similarly treated control solution containing 0.2 mL of 0.02 N sulfuric acid (0.2%).

Chromium Picolinate, Chromium Chloride, Chromic Chloride Suppliers:

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