Pyruvic acid - ≥98%(T) , CAS No.127-17-3

CAS: 127-17-3 Cat. No.: P104138 Formula: C3H4O3 Molecular Weight: 88.06 Beilstein Registry Number: 506211 EC Number: 204-824-3
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(T)
Synonyms
13C Labeled pyruvic acid | Brenztraubensaeure | 2-Oxopropansaure | bmse000112 | B3CFF0AD-2F35-484C-B062-4AC88A1B2830 | Tox21_303284 | C00022 | EINECS 204-824-3 | 2-Oxopropanoic acid, Pyroracemic acid | AKOS000118803 | AMY6082 | Pyruvic acid (natural) | Py
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
★
Size
USA
Germany (EU)*
Price
Qty
25g
P104138-25g
5 In stock
—
$13.90
100g
P104138-100g
3 In stock
—
$39.90
500g
P104138-500g
Made to order · 8–12 wks
$109.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥98%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 92 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

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.

Application
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.

Specifications

Synonyms
13C Labeled pyruvic acid | Brenztraubensaeure | 2-Oxopropansaure | bmse000112 | B3CFF0AD-2F35-484C-B062-4AC88A1B2830 | Tox21_303284 | C00022 | EINECS 204-824-3 | 2-Oxopropanoic acid, Pyroracemic acid | AKOS000118803 | AMY6082 | Pyruvic acid (natural) | Py
Specifications & Purity
≥98%(T)
Biochemical and Physiological Mechanisms
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 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%(T)
Names and Identifiers
Pubchem Sid
Canonical Smiles
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)
Isomeric SMILES
CC(=O)C(=O)O
WGK Germany
3
UN Number
3265
Molecular Weight
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=

Documentation

📋 Safety Data Sheet (SDS)

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

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

✅ 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
ClassKeto acids and derivatives
SubclassAlpha-keto acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAlpha-keto acids and derivatives
Alternative Parents Alpha-hydroxy ketones  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A10 SLC16A10 protein (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO (473 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTBP2 Tchem C-terminal-binding protein 2 (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dapA Dihydrodipicolinate synthase (65 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a20 Solute carrier family 22 member 20 (86 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a6 Solute carrier family 22 member 6 (141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slco2a1 Solute carrier organic anion transporter family member 2A1 (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A085R Prolyl 4-hydroxylase (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates (CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

43 results found

Lot NumberCertificate TypeDateItem
G2629663G2629663Certificate of AnalysisJul 04, 2026 P104138
G2629416G2629416Certificate of AnalysisJul 04, 2026 P104138
G2629414G2629414Certificate of AnalysisJul 04, 2026 P104138
G2629413G2629413Certificate of AnalysisJul 04, 2026 P104138
C2613470C2613470Certificate of AnalysisFeb 28, 2026 P104138
C2613472C2613472Certificate of AnalysisFeb 28, 2026 P104138
C2613487C2613487Certificate of AnalysisFeb 28, 2026 P104138
H2506497H2506497Certificate of AnalysisJul 05, 2025 P104138
H2506496H2506496Certificate of AnalysisJul 05, 2025 P104138
H2506365H2506365Certificate of AnalysisJul 05, 2025 P104138
L2516065L2516065Certificate of AnalysisDec 02, 2024 P104138
L2424539L2424539Certificate of AnalysisDec 02, 2024 P104138
L2424538L2424538Certificate of AnalysisDec 02, 2024 P104138
L2424537L2424537Certificate of AnalysisDec 02, 2024 P104138
L2424536L2424536Certificate of AnalysisDec 02, 2024 P104138
F2623065F2623065Certificate of AnalysisDec 02, 2024 P104138
I2406444I2406444Certificate of AnalysisAug 26, 2024 P104138
I2406442I2406442Certificate of AnalysisAug 26, 2024 P104138
I2406443I2406443Certificate of AnalysisAug 26, 2024 P104138
D2415102D2415102Certificate of AnalysisApr 02, 2024 P104138
D2415103D2415103Certificate of AnalysisApr 02, 2024 P104138
D2415104D2415104Certificate of AnalysisApr 02, 2024 P104138
D2415108D2415108Certificate of AnalysisApr 02, 2024 P104138
D2415107D2415107Certificate of AnalysisApr 02, 2024 P104138
D2415106D2415106Certificate of AnalysisApr 02, 2024 P104138
D2415105D2415105Certificate of AnalysisApr 02, 2024 P104138
L2121269L2121269Certificate of AnalysisSep 21, 2023 P104138
A2411003A2411003Certificate of AnalysisMay 24, 2023 P104138
F2308598F2308598Certificate of AnalysisMay 24, 2023 P104138
L2312020L2312020Certificate of AnalysisMay 24, 2023 P104138
F2308460F2308460Certificate of AnalysisMay 24, 2023 P104138
F2308461F2308461Certificate of AnalysisMay 24, 2023 P104138
K2217924K2217924Certificate of AnalysisSep 13, 2022 P104138
K2217954K2217954Certificate of AnalysisSep 13, 2022 P104138
K2217973K2217973Certificate of AnalysisSep 13, 2022 P104138
K2217982K2217982Certificate of AnalysisSep 13, 2022 P104138
K2217983K2217983Certificate of AnalysisSep 13, 2022 P104138
E2305079E2305079Certificate of AnalysisSep 13, 2022 P104138
B2423058B2423058Certificate of AnalysisSep 13, 2022 P104138
G2304051G2304051Certificate of AnalysisSep 13, 2022 P104138
H2017072H2017072Certificate of AnalysisJun 16, 2022 P104138
H2230018H2230018Certificate of AnalysisDec 02, 2021 P104138
H2218100H2218100Certificate of AnalysisDec 02, 2021 P104138
Chemical and Physical Properties
SolubilityMiscible with chloroform and methanol.
SensitivityHeat,Light & Air Sensitive.
Refractive Index1.426-1.43
Flash Point(°F)82℃
Flash Point(°C)82℃
Boil Point(°C)165℃
Melt Point(°C)11-13 °C
Molecular Weight88.060 g/mol
XLogP3-0.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass88.016 Da
Monoisotopic Mass88.016 Da
Topological Polar Surface Area54.400 Ų
Heavy Atom Count6
Formal Charge0
Complexity84.000
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 Count1
Documents & Articles
Aldol Condensation Reaction
Guidelines For Common Cell Culture Media
Technical Analysis and Clinical Applications of Lactate Dehydrogenase
Niacin (Vitamin B3): Structural Features, Metabolic Roles, and Application Landscape
Key Enzymes in Amino Acid Metabolism: A Mechanistic Framework and Research Applications
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
Acetyl-Group Metabolic Enzyme Network and In Vitro Enzymology Analysis
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
TCA Cycle Metabolite Detection Methods and Result Interpretation
Probiotics, Prebiotics, and Postbiotics in Skin Care: Conceptual Distinctions, Mechanisms of Action, and Their Applications in the Care of Dry, Itchy, and Rough Skin
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

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