Uracil GMP Bioburden Endotoxin Tested

GMP Process Chemical

IPEC GMP Manufactured Product

URACIL

BET*, GMP
Product Code: URAC-4250

*Bioburden and Endotoxin Tested

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Lead Time: Inquire

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Product Code: URAC-4250

Suitable for use as a cGMP chemical in pharmaceutical manufacturing processes.

Uracil is important for the detoxification of many carcinogens and is also used to detoxify many drugs such as cannabinoids and opioids. Uracil can be used for drug delivery and as an intermediate to compounds used in anticancer drugs. Other derivatives are used in pesticides and antiphotosynthetic herbicides as well as in the synthesis of caffeine. Uracil is used as a coenzyme and allosteric regulator during biochemical reactions and for polysaccharide biosynthesis and transportation of sugars containing aldehydes.

CAS #: 66-22-8
Formula: C₄H₄N₂O₂F.W.: 112.09 g/mol

Product Specifications

ANALYSIS

SPECIFICATIONS

Appearance and Color

White to Slightly Yellow Powder

Assay, Dried Basis

> = 98%

Chloride

< = 100 ppm

Endotoxin

< = 3 EU/g

Heavy Metals (Pb)

< = 20 ppm

Identification, IR

Conforms to Reference Standard

Loss on Drying

< = 0.50%

Melting Point

> = 300°C

Reaction

Passes Test

Residue on Ignition

< = 0.10%

Solubility

Passes Test

Sulfate

< = 400 ppm

TAMC

< = 100 CFU/g

Printable Version

Key Product Features:

The manufacturing of Uracil, URAC-4250 is performed at BioSpectra's Bangor, PA facility.
Appears as white to slightly yellow powder
Manufactured in accordance with IPEC
Manufactured in an enzyme free, hormone free, and animal free environment
Contains no known major food allergens
The final product and its raw materials are not derived from nor come into contact with animal parts, animal products, and/or animal byproducts or derivatives.
Is not subject to genetic modification
Synonyms: 2,4-Dihydroxypyrimidine; 2,4(1H,3H)-Pyrimidinedione; 2,4-Pyrimidinediol.

Shelf-Life Policy:

Unless otherwise noted on the Shelf-Life Statement and CoA, this product has a 2-year retest date supported by a 3-year ICH Q1 Stability Study (if one is completed).

Storage & Shipping:

Refer to SDS.

Package Sizes:

10kg, 25kg, and 50kg

Bulk GMP Fine Chemicals exclusively manufactured in North America

American Manufactured - FDA Registered GMP Facilities: Parenteral Excipients, GMP Small Molecule Intermediates, GMP Biological Buffers, Parenteral Carbohydrates, GMP Chlorinated Amino Acids, GMP Solutions in Sterile Single Use Packaging and other Reagent & GMP Fine Chemicals.