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Merck
CN

O2875

乳清酸 钾盐

≥98%

别名:

6-Carboxy-2,4-dihydroxypyrimidine, Uracil-6-carboxylic acid

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关于此项目

线性分子式:
C5H3N2O4K
化学文摘社编号:
分子量:
194.19
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
246-341-0
MDL number:
Assay:
≥98%
Form:
powder
Solubility:
1 M NaOH: 25 mg/mL, clear to slightly hazy, colorless to faintly yellow
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Quality Segment

assay

≥98%

form

powder

solubility

1 M NaOH: 25 mg/mL, clear to slightly hazy, colorless to faintly yellow

SMILES string

[K+].[O-]C(=O)C1=CC(=O)NC(=O)N1

InChI

1S/C5H4N2O4.K/c8-3-1-2(4(9)10)6-5(11)7-3;/h1H,(H,9,10)(H2,6,7,8,11);/q;+1/p-1

InChI key

DHBUISJCVRMTAZ-UHFFFAOYSA-M

Application

Orotic acid (OA) is an intermediate in de novo pyrimidine biosynthesis that 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.


存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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