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Key Documents

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Safety Information

W245704

Sigma-Aldrich

Ethyl pyruvate

≥97%

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About This Item

Linear Formula:
CH3COCOOC2H5
CAS Number:
617-35-6
Molecular Weight:
116.12
FEMA Number:
2457
Beilstein:
1071466
EC Number:
210-511-2
Council of Europe no.:
430
MDL number:
MFCD00009123
UNSPSC Code:
12164502
PubChem Substance ID:
24901103
Flavis number:
9.442

biological source

synthetic

grade

Halal

reg. compliance

FDA 21 CFR 172.515

Assay

≥97%

refractive index

n20/D 1.404 (lit.)

bp

144 °C (lit.)

density

1.045 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

ethereal; vegetable; fruity; rum; sweet

SMILES string

CCOC(=O)C(C)=O

InChI

1S/C5H8O3/c1-3-8-5(7)4(2)6/h3H2,1-2H3

InChI key

XXRCUYVCPSWGCC-UHFFFAOYSA-N

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Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H226,H314

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

114.8 °F - closed cup

Flash Point(C)

46 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBD1796V
STBD7235V
STBC8467V
STBC7766V
MKBG9345V

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Runkuan Yang et al.
Critical care (London, England), 16(1), R9-R9 (2012-01-18)
Inflammation may critically affect mechanisms of liver injury in acetaminophen (APAP) hepatotoxicity. Kupffer cells (KC) play important roles in inflammation, and KC depletion confers protection at early time points after APAP treatment but can lead to more severe injury at
M-L Li et al.
International journal of immunopathology and pharmacology, 25(4), 955-965 (2013-01-10)
High mobility group box B1 (HMGB1)-receptor for advanced glycation end products (RAGE) axis has been previously known to be involved in carcinogenesis and development of multiple malignancies. Some studies have confirmed that Ethyl pyruvate (EP), a potent inhibitor of HMGB1
M P Fink
Journal of internal medicine, 261(4), 349-362 (2007-03-30)
Ethyl pyruvate (EP) is a simple derivative of the endogenous metabolite, pyruvic acid. Treatment with EP has been shown to improve survival and/or ameliorate organ dysfunction in a wide variety of preclinical models of critical illnesses, such as severe sepsis
Mitchell P Fink
Current opinion in clinical nutrition and metabolic care, 5(2), 167-174 (2002-02-15)
Reactive oxygen species are reactive, partly reduced derivatives of molecular oxygen. Important reactive oxygen species in biological systems include superoxide radical anion, hydrogen peroxide, and hydroxyl radical. Peroxynitrite, is another important species in biological systems. A variety of enzymatic and
Mitchell P Fink
Current drug targets, 8(4), 515-518 (2007-04-14)
Pyruvic acid is a three-carbon alpha-ketocarboxylic acid that plays a central role in intermediary metabolism, being the final product of glycolysis and the starting substrate for the tricarboxylic acid cycle. Ethyl pyruvate, which is a simple aliphatic ester derived from
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