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

Name: Pyruvic acid - 10mM in DMSO , CAS No.127-17-3
Brand: Aladdin Scientific
SKU: P421121
Availability: InStock

CAS: 127-17-3 Cat. No.: P421121 Summenformel: C₃H₄O₃ Molekulargewicht: 88.06 Beilstein Registry Number: 506211 EG-Nummer: 204-824-3

92 Citations COA

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Pyruvic acid - 10mM in DMSO CAS No(127-17-3) by Aladdin Scientific

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QUALITÄT & REINHEIT 10mM in DMSO

Synonyms

Storage

Store at -80°C

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Dry ice packs + Cold packs

Übersicht Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Warum diese Qualität

10mM in DMSO für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at -80°C Versand Dry ice packs + Cold packs. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

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Literaturbeleg

In 92 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

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.

Spezifikationen

Synonyme

Spezifikationen & Reinheit

10mM in DMSO

Biochemische und physiologische Mechanismen

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

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

Pubchem Sid

528769247

Kanonisches Lächeln

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)

Isomere SMILES

CC(=O)C(=O)O

WGK Deutschland

UN-Nummer

3265

Molekulargewicht

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=

Dokumentation

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Taxonomic Classification

Taxonomy Tree

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

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Klasse	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
Beschreibung	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

3D-Struktur

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SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

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FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

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SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

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

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Hdac6 Histone deacetylase 6 (222 Activities)

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dapA Dihydrodipicolinate synthase (65 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Slc22a20 Solute carrier family 22 member 20 (86 Activities)

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Slc22a6 Solute carrier family 22 member 6 (141 Activities)

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

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Slc16a10 Monocarboxylate transporter 10 (73 Activities)

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SARS-CoV-2 (38078 Activities)

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A085R Prolyl 4-hydroxylase (72 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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Lot Number	Certificate Type	Datum	Artikel
K2210190	Certificate of Analysis	Jul 13, 2026	P421121

Chemische und physikalische Eigenschaften

Empfindlichkeit	Heat,Light & Air Sensitive.
Brechungsindex	1.426-1.43
Flammpunkt (°F)	82℃
Flammpunkt (°C)	82℃
Siedepunkt (°C)	165℃
Schmelzpunkt (°C)	11-13 °C
Molekulargewicht	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

FAQs und Artikel

Technical Analysis and Clinical Applications of Lactate Dehydrogenase

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

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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

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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

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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

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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

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High-performance liquid chromatography Porous Graphitic Carbon

TCA Cycle Metabolite Detection Methods and Result Interpretation

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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

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skin care Probiotics

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📚 Zitationen nach Anwendung

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

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

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