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W200344

Sigma-Aldrich

Acetaldehyde solution

natural, 50 wt. % ethanol, FG

Synonym(s):

Acetic aldehyde, Ethanal, Ethylaldehyde

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About This Item

Linear Formula:
CH3CHO
CAS Number:
Molecular Weight:
44.05
FEMA Number:
2003
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
5.001
NACRES:
NA.21

grade

FG
Kosher
natural

Quality Level

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

vapor pressure

25.89 psi ( 55 °C)
5.54 psi ( 20 °C)

Assay

≥95% (GC)

form

liquid

concentration

45.00-55.00% (titration by hydroxylamine)
50 wt. % ethanol

refractive index

n20/D 1.39

bp

61-82 °C

density

0.868 g/mL at 20 °C
0.882 g/mL at 25 °C

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

fruity; ethereal; pungent

storage temp.

2-8°C

SMILES string

[H]C(C)=O

InChI

1S/C2H4O/c1-2-3/h2H,1H3

InChI key

IKHGUXGNUITLKF-UHFFFAOYSA-N

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Legal Information

For R&D Use and/or for Food Manufacturing only

Signal Word

Danger

Hazard Statements

Hazard Classifications

Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Acetaldehyde puriss. p.a., anhydrous, ≥99.5% (GC)

Sigma-Aldrich

00070

Acetaldehyde

Acetaldehyde United States Pharmacopeia (USP) Reference Standard

USP

1002811

Acetaldehyde

M Becker et al.
Journal of chromatography. A, 1281, 115-126 (2013-02-13)
Gas chromatographic analysis of complex carbohydrate mixtures requires highly effective and reliable derivatisation strategies for successful separation, identification, and quantitation of all constituents. Different single-step (per-trimethylsilylation, isopropylidenation) and two-step approaches (ethoximation-trimethylsilylation, ethoximation-trifluoroacetylation, benzoximation-trimethylsilylation, benzoximation-trifluoroacetylation) have been comprehensively studied with regard
Marjie L Hard et al.
Placenta, 24(2-3), 149-154 (2003-02-05)
Significant interindividual variability exists following maternal alcohol consumption; not all children born to alcoholic women manifest the symptoms associated with foetal alcohol spectrum disorder (FASD). To investigate the potential role of the placenta as a source of variability by determining
Tetsuji Yokoyama et al.
Alcoholism, clinical and experimental research, 29(4), 622-630 (2005-04-19)
Elevated mean corpuscular volume (MCV) is a traditional biological marker for alcohol abuse and alcoholism, but the underlying mechanism is unclear. Three recent epidemiologic studies consistently showed that MCV was elevated by alcohol drinking more markedly among individuals with genetically
Dirk W Lachenmeier et al.
Addiction (Abingdon, England), 104(4), 533-550 (2009-04-02)
In addition to being produced in ethanol metabolism, acetaldehyde occurs naturally in alcoholic beverages. Limited epidemiological evidence points to acetaldehyde as an independent risk factor for cancer during alcohol consumption, in addition to the effects of ethanol. This study aims
Mercè Correa et al.
Neuroscience and biobehavioral reviews, 36(1), 404-430 (2011-08-10)
Mainly known for its more famous parent compound, ethanol, acetaldehyde was first studied in the 1940s, but then research interest in this compound waned. However, in the last two decades, research on acetaldehyde has seen a revitalized and uninterrupted interest.

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