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About This Item
Linear Formula:
KOP(O)(OH)OC(=CH2)CO2H
CAS Number:
Molecular Weight:
206.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-247-0
Beilstein/REAXYS Number:
4603446
MDL number:
Assay:
99%
Form:
powder
Quality Level
assay
99%
form
powder
mp
175 °C (dec.) (lit.)
functional group
carboxylic acid, phosphate
storage temp.
−20°C
SMILES string
[K+].OC(=O)C(=C)OP(O)([O-])=O
InChI
1S/C3H5O6P.K/c1-2(3(4)5)9-10(6,7)8;/h1H2,(H,4,5)(H2,6,7,8);/q;+1/p-1
InChI key
SOSDSEAIODNVPX-UHFFFAOYSA-M
Application
Substrate for many kinase reactions.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ernesto Arias-Palomo et al.
Molecular cell, 74(1), 173-184 (2019-02-25)
In cells, dedicated AAA+ ATPases deposit hexameric, ring-shaped helicases onto DNA to initiate chromosomal replication. To better understand the mechanisms by which helicase loading can occur, we used cryo-EM to determine sub-4-Å-resolution structures of the E. coli DnaB⋅DnaC helicase⋅loader complex with
Jemila C Kester et al.
Journal of bacteriology, 203(4) (2020-11-25)
The ClpP1P2 proteolytic complex is essential in Mycobacterium tuberculosis Proteolysis by ClpP1P2 requires an associated ATPase, either ClpX or ClpC1. Here, we sought to define the unique contributions of the ClpX ATPase to mycobacterial growth. We formally demonstrated that ClpX
Hui Hong et al.
Cell chemical biology, 26(4), 493-501 (2019-02-05)
Malayamycin A is an unusual bicyclic C-nucleoside, with interesting antiviral, antifungal, and anticancer bioactivity. We report here the discovery and characterization of the biosynthetic pathway to malayamycin by using genome mining of near-identical clusters both from the known producer Streptomyces
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 860077-250MG | 04061833032602 |
| 860077-1G | 04061833032596 |