Product Detail
D-Glucuronic acid
Glucuronic acid Carbohydrates
Stock Status: In Stock
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For Research & Analytical Purposes. Not for Personal use.
Category
Carbohydrates
API Family
Glucuronic acid
Storage
Store at refrigerator (2-8°C) for long term storage
Hazard Information
Refer MSDS for accurate information.
D-Glucuronic acid Product Information
D-Glucuronic acid is listed under Carbohydrates. It is associated with Glucuronic acid and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-25432.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.
Technical Data
Product Name
D-Glucuronic acid
CAS No.
6556-12-3
CAT No.
CS-T-25432
Molecular Formula
C₆H₁₀O₇
Molecular Weight
194.14
Category
API Family
Storage Condition
Store at refrigerator (2-8°C) for long term storage
SMILES
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O
IUPAC Name
(3S,5R)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid
Purity by HPLC
Not less than 90%
Hazard Compound
Refer MSDS for accurate information.
Description
Overview
"D-Glucuronic acid is widely distributed in the plant and animal kingdoms. D-Glucuronic acid usually occurs in ??paired?? form as a glycosidic combination with phenols, alcohols. Such glucuronides form in the liver to detoxify poisonous hydroxyl-containing substances. The glucuronides present in normal urine are those of phenol, cresol, and indoxyl. After the ingestion of poisons such as morphine, chloral hydrate, camphor, or turpentine, glucuronides formed with the poison or its hydroxylated derivatives appear in the urine. "
Synonyms
(3S,5R)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid
Application Notes
"D-Glucuronic acid is widely distributed in the plant and animal kingdoms. D-Glucuronic acid usually occurs in ??paired?? form as a glycosidic combination with phenols, alcohols. Such glucuronides form in the liver to detoxify poisonous hydroxyl-containing substances. The glucuronides present in normal urine are those of phenol, cresol, and indoxyl. After the ingestion of poisons such as morphine, chloral hydrate, camphor, or turpentine, glucuronides formed with the poison or its hydroxylated derivatives appear in the urine. "
References
"Levene, M,, et al,: J, Biol, Chem,, 92, 257 (1931), Miyamoto, I,, et al,: Anal, Biochem,, 115, 308 (1981), "
