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Orotic acid, monohydrate

Orotic acid, monohydrate

Orotic Acid Monohydrate

SKU: 02102508-CF

Synonyms
2,6-Dioxo-1,2,3,6-tetrahydro-4-pyrimidinecarboxylic acid; Uracil-6-carboxylic acid; Whey factor; Animal galactose factor; Oropur; Orotyl; 6-Carboxy-2,4-dihydroxypyrimidine
CAS Number:
50887-69-9
Molecular Formula:
C5H4N2O4 • H2O
Molecular Weight:
174.112 g/mol
Beilstein Registry Number:
7604036
MDL Number:
MFCD00149398
Product Description

Orotic Acid Monohydrate

Application Notes

Orotic acid (OA) may be used to study the specificity and kinetics of orotate phosphoribosyltransferase (OPRT) which catalyzes the reversible phosphoribosyl transfer from 5′-phospho-α-d-ribose 1′-diphosphate (PRPP) to orotic acid (OA), forming pyrophosphate and orotidine 5′-monophosphate (OMP). Orotic acid is used as a starting material for the potential commercial bioproduction of uridine 5′-monophosphate (UMP) by microbes such as Corynebacterium ammoniagenes (ATCC 6872) or Saccharomyces cerevisiae. OA may be used to study the AMPK/SREBP-1 dependent cell signaling pathway and transcription regulation mechanisms that induce hepatic lipogenesis.

Usage Statement

Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.

Key Applications

Used in study of biosynthesis of pyrimidine nucleobases

Specifications
SKU 02102508-CF
Alternate Names 2,6-Dioxo-1,2,3,6-tetrahydro-4-pyrimidinecarboxylic acid; Uracil-6-carboxylic acid; Whey factor; Animal galactose factor; Oropur; Orotyl; 6-Carboxy-2,4-dihydroxypyrimidine
Application Notes Orotic acid (OA) may be used to study the specificity and kinetics of orotate phosphoribosyltransferase (OPRT) which catalyzes the reversible phosphoribosyl transfer from 5′-phospho-α-d-ribose 1′-diphosphate (PRPP) to orotic acid (OA), forming pyrophosphate and orotidine 5′-monophosphate (OMP). Orotic acid is used as a starting material for the potential commercial bioproduction of uridine 5′-monophosphate (UMP) by microbes such as Corynebacterium ammoniagenes (ATCC 6872) or Saccharomyces cerevisiae. OA may be used to study the AMPK/SREBP-1 dependent cell signaling pathway and transcription regulation mechanisms that induce hepatic lipogenesis.
Base Catalog Number 102508
Beilstein Registry Number 7604036
CAS # 50887-69-9
Format Powder
Hazard Statements H315-H319-H335
Molecular Formula C5H4N2O4 • H2O
Molecular Weight 174.112 g/mol
Personal Protective Equipment Dust mask, Eyeshields, Gloves
Safety Symbol GHS07
Usage Statement Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.
UV Visible Absorbance λ max (water) 205 nm (280 nm) ± 5 nm
Documents

Certificates of Analysis

Certificates of Analysis
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Datasheets

Datasheets
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Material Safety Data Sheet

Material Safety Data Sheet
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Material Safety Data Sheet
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Material Safety Data Sheet
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