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Prova documentale

Citato in 92 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Panoramica

Pyruvic acid was used to study the cultivation of previously undescribed soil bacteria as micro colonies using soil substrate membrane system. Pyruvic acid was used to develop a new method for simultaneous determination of organic acids in red wine and must using liquid chromatography.

Specifiche

Sinonimi

Specifiche e purezza

10mM in DMSO

Meccanismi biochimici e fisiologici

Pyruvic acid reacts with N-acetyl mannosamine by an aldol-type condensation to form sialic acid. Pyruvic acid is a component of commercial red seaweed polysaccharide.In muscle, pyruvic acid (derived from glycogen) is reduced to lactic acid during exertion

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Nomi e identificatori

Pubchem Sid

528769247

Sorrisi canonici

CC(=O)C(=O)O

IUPAC Name

2-oxopropanoic acid

InChIKey

LCTONWCANYUPML-UHFFFAOYSA-N

INCHI

1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)

Isomeri SMILES

CC(=O)C(=O)O

WGK Germania

Numero UN

3265

Peso molecolare

88.06

Beilstein

506211

Reaxy-Rn

506211

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506211&ln=

Documentazione

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<<<<<<< HEAD Scarica SDS → ======= Scarica SDS → >>>>>>> release248-p3

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Keto acids and derivatives
    - Subclass Alpha-keto acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Keto acids and derivatives
Subclass	Alpha-keto acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Alpha-keto acids and derivatives
Alternative Parents	Alpha-hydroxy ketones Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Alpha-keto acid - Alpha-hydroxy ketone - Ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Descrizione	This compound belongs to the class of organic compounds known as alpha-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the adjacent carbon.
External Descriptors	Oxo fatty acids
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Struttura 3D

Obiettivi associati (umani)

SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

Discover Target: SLC16A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)

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SLC16A10 SLC16A10 protein (28 Activities)

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FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO (473 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CTBP2 Tchem C-terminal-binding protein 2 (36 Activities)

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Obiettivi associati (non umani)

Hdac6 Histone deacetylase 6 (222 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

dapA Dihydrodipicolinate synthase (65 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc22a20 Solute carrier family 22 member 20 (86 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc22a6 Solute carrier family 22 member 6 (141 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slco2a1 Solute carrier organic anion transporter family member 2A1 (47 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc16a10 Monocarboxylate transporter 10 (73 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SARS-CoV-2 (38078 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A085R Prolyl 4-hydroxylase (72 Activities)

Discover Target: A085R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Certificati (CoA, COO, BSE/TSE e tabella di analisi)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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1 results found

Lot Number	Certificate Type	Data	Oggetto
K2210190	Certificate of Analysis	Jul 13, 2026	P421121

Proprietà chimiche e fisiche

Sensibilità	Heat,Light & Air Sensitive.
Indice di rifrazione	1.426-1.43
Punto di infiammabilità (°F)	82℃
Punto di infiammabilità (°C)	82℃
Punto di ebollizione (°C)	165℃
Punto di fusione (°C)	11-13 °C
Peso molecolare	88.060 g/mol
XLogP3	-0.300
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	88.016 Da
Monoisotopic Mass	88.016 Da
Topological Polar Surface Area	54.400 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	84.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Domande frequenti e articoli

Technical Analysis and Clinical Applications of Lactate Dehydrogenase

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Lactate Dehydrogenase LDH EC 1.1.1.27

Niacin (Vitamin B3): Structural Features, Metabolic Roles, and Application Landscape

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Pharmaceutical Intermediates Niacin Vitamin B3 Nicotinamide NADP+ Niacin equivalents Nutritional fortification Feed additive

Key Enzymes in Amino Acid Metabolism: A Mechanistic Framework and Research Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

metabolic flux amino acid metabolism key enzymes aminotransferases glutamate dehydrogenase branched-chain amino acid metabolism threonine metabolism D-amino acids stable isotope tracing compartmentalization

From “Reduction First, Then Acylation” to “Direct Amidation”: An Unconventional Route to Amide Bond Formation from Nitro and Nitroso Substrates with α-Keto Carboxylic Acids

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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Amidation reaction Amide bond construction Nitro compounds

Acetyl-Group Metabolic Enzyme Network and In Vitro Enzymology Analysis

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Epigenetic Regulation Acetyl-Group Metabolism Acetyl-Coa Acetyltransferases Deacetylases Pathway Analysis In Vitro Enzymology Central Carbon Metabolism

Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

High-performance liquid chromatography Porous Graphitic Carbon

TCA Cycle Metabolite Detection Methods and Result Interpretation

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

TCA cycle metabolic flux citrate LC-MS/MS Tricarboxylic acid cycle α-ketoglutarate metabolite detection succinate

Probiotics, Prebiotics, and Postbiotics in Skin Care: Conceptual Distinctions, Mechanisms of Action, and Their Applications in the Care of Dry, Itchy, and Rough Skin

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

skin care Probiotics

Citations of This Product

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Recensioni

📚 Citazioni per applicazione

Electrochemistry & battery electrolyte18

Organic synthesis — reaction medium54

Extraction & workup solvent29

Chromatography (HPLC / GC / TLC)8

Controlled-release & nanoparticle carrier3

Other applications39

Spectroscopy sample preparation8

Industrial & non-pharma application5

Drug / compound screening7

Cross-coupling reactions5

Nanoparticle / material biocompatibility1

Cancer cell line characterization1

Cell viability1

Polymer synthesis & polymerization4

Film coating1

Cytotoxicity screening2

Crystallization & recrystallization1

Topical & ophthalmic formulation1

Visualizza tutte le 92 citazioni →

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Pyruvic acid - 10mM in DMSO , CAS No.127-17-3

Stoccaggio e spedizione

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