Finoric LLC

Carbamide Peroxide

Carbamide Peroxide, Pure and USP Grade Supplier, Manufacturer's Representative

FInOrIC, etymologically derived from our business line of Fine Inorganic, Organic and Industrial Chemicals, is the internationally preferred source for Chemicals. With customers in 55 countries across 5 continents, we source and sell most chemicals. Backed by owned full fledged chemical manufacturing facilities in Midland & Houston Area Texas with associated manufacturing sites in India, Dubai, China and USA we are a truly multi-national chemical manufacturer & distributor. Fracturing and Fracking Industry can rely on our 24x7 - 365days service including week-end deliveries.

DESCRIPTION

Carbamide peroxide is a solid composed of equal amounts of hydrogen peroxide and urea. This compound is a white crystalline solid, which dissolves in water to give free hydrogen peroxide. Often called Hydrogen peroxide - urea, used in the dental applications, it is used as a source of hydrogen peroxide for bleaching, disinfection, and oxidation. Hydrogen peroxide - urea is mainly used as a disinfecting and bleaching agent in cosmetics and pharmaceuticals. As a drug, this compound is used in some preparations for the whitening of teeth. It is also used to relieve minor inflammation of gums, oral mucosal surfaces and lips including canker sores and dental irritation and to emulsify and disperse ear wax.

Carbamide Peroxide USP Grade
CH6N2O3 -- 94.07
Urea compound with hydrogen peroxide (1:1) [CAS Number 124-43-6].
Carbamide Peroxide contains not less than 96.0 percent and not more than 102.0 percent of CH6N2O3.

Identification:
A: Mix 1 mL of a solution (1 in 10) of it with 1 mL of nitric acid: a white, crystalline precipitate is formed.
B: A solution of it (1 in 10) responds to the tests for Peroxide.

Assay:
Transfer about 100 mg of Carbamide Peroxide, accurately weighed, to a 500-mL iodine flask with the aid of 25 mL of water, add 5 mL of glacial acetic acid, and mix. Add 2 g of potassium iodide and 1 drop of ammonium molybdate, insert the stopper, and allow to stand in the dark for 10 minutes. Titrate the liberated iodine with 0.1 N sodium thiosulfate, adding 3 mL of starch as the endpoint is approached. Each mL of 0.1 N sodium thiosulfate is equivalent to 4.704 mg of CH 6N2O3.

Most of our partners facilities of MANUFACTURE BULK DRUGS/API, EXCIPIENTS, PHARMACEUTICALS (IP/BP/USP/NF/PH. EUR./JP), SPECIALITY CHEMICALS (PURE/AR/ACS), MINERAL FORTIFIERS (FCC). OUR MANUFACTURING FACILITY IS GLP, GMP (FDA) APPROVED, ISO 9001, ISO 14001, ISO 22000, FSSC 22000, FSSAI, KOSHER, HALAL, COPP AND WHO-GMP CERTIFIED.

Good Manufacturing Practice Certified by World Health Organization (WHO-GMP)
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