Phospho(enol)pyruvic acid monopotassium salt - 10mM in Water , CAS No.4265-07-0

CAS: 4265-07-0 Cat. No.: P423930 Peso molecular: 206.13 Beilstein Registry Number: 4603446 Número EC: 224-247-0
Disponible para pedir
GRADE & PURITY 10mM in Water
Synonyms
4265-07-0|Potassium 1-carboxyvinyl hydrogenphosphate|PHOSPHOENOLPYRUVIC ACID MONOPOTASSIUM SALT|Phospho(enol)pyruvic acid monopotassium salt|PEP-K|phosphoenolpyruvate potassium salt|MFCD00044476|2-Propenoic acid, 2-(phosphonooxy)-, monopotassium salt|pota
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
P423930-1ml
1

58,90US$

69,90US$
Guardar 11,00 US$ (15.74%)
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Why this grade

10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Phospho(enol)pyruvic acid (PEP) acts as an inhibitor of hexokinase, phosphoglucose isomerase, phosphofructokinase and aldolase. It is a bifunctional carbohydrate, which exhibits antioxidant property. PEP may be a potential organ preservation agent in clinical transplantation.

Specifications

Sinónimos
4265-07-0 | Potassium 1-carboxyvinyl hydrogenphosphate | PHOSPHOENOLPYRUVIC ACID MONOPOTASSIUM SALT | Phospho(enol)pyruvic acid monopotassium salt | PEP-K | phosphoenolpyruvate potassium salt | MFCD00044476 | 2-Propenoic acid, 2-(phosphonooxy)-, monopotassium salt | pota
Especificaciones y pureza
10mM in Water
Mecanismos bioquímicos y fisiológicos
Phospho(enol)pyruvic acid (PEP) is involved in glycolysis and gluconeogeneis. In glycolysis, PEP is metabolized by Pyruvate Kinase to yield pyruvate. In plants, PEP is involved in the formation of aromatic amino acids as well as in the carbon fixation pat
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasC=C(C(=O)O)OP(=O)(O)[O-].[K+]
IUPAC Namepotassium;1-carboxyethenyl hydrogen phosphate
InChIKeySOSDSEAIODNVPX-UHFFFAOYSA-M
INCHI1S/C3H5O6P.K/c1-2(3(4)5)9-10(6,7)8;/h1H2,(H,4,5)(H2,6,7,8);/q;+1/p-1
Isómeros SMILES C=C(C(=O)O)OP(=O)(O)[O-].[K+]
WGK Alemania 3
Peso molecular 206.13
Beilstein 4603446
Reaxy-Rn 4603446
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4603446&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseOrganic phosphoric acids and derivatives
SubclassPhosphate esters
Intermediate Tree Nodes Not available
Direct ParentPhosphate esters
Alternative Parents Monocarboxylic acids and derivatives  Carboxylic acids  Organic potassium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Organic cations  
Molecular FrameworkAliphatic acyclic compounds
Substituents Phosphoric acid ester - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic potassium salt - Organic salt - Organooxygen compound - Carbonyl group - Organic cation - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phosphate esters. These are organic compounds containing phosphoric acid ester functional group, with the general structure R1P(=O)(R2)OR3. R1,R2 = O,N, or halogen atom; R3 = organyl group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadHygroscopic
Punto de fusión (°C)170°C
Peso molecular206.130 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass205.938 Da
Monoisotopic Mass205.938 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity212.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
Referencias
1. Jinling Cui, Mingzhu Yan, Xiaoyi Liu, Shutao Yin, Shangyun Lu, Lihong Fan, Hongbo Hu.  (2019)  Inorganic Selenium Induces Nonapoptotic Programmed Cell Death in PC-3 Prostate Cancer Cells Associated with Inhibition of Glycolysis.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:31513389] [10.1021/acs.jafc.9b03875]
2. Wenya Ou, Shuai Luo, Jing Tang, Guangyi Wang, Lin Tang.  (2025)  A reduced graphene oxide-based enzyme-modified screen-printed electrode for highly sensitive acetate detection in anaerobic fermentation process.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2025.147723]
Calculadoras de soluciones
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