
Acetaldehyde - Wikipedia
Many microbes produce acetaldehyde from ethanol, but they have a lower capacity to eliminate the acetaldehyde, which can lead to the accumulation of acetaldehyde in saliva, stomach acid, …
Acetaldehyde | Alcohol Metabolism, Carcinogen, Toxicity ...
Acetaldehyde (CH3CHO), an aldehyde used as a starting material in the synthesis of 1-butanol (n-butyl alcohol), ethyl acetate, perfumes, flavourings, aniline dyes, plastics, synthetic rubber, …
Acetaldehyde is mainly used as an intermediate in the synthesis of other chemicals. It is ubiquitous in the environment and may be formed in the body from the breakdown of ethanol.
What Does Acetaldehyde Do to Your Body? - Biology Insights
Jul 29, 2025 · Acetaldehyde is a chemical compound naturally present in some foods and produced within the human body. It forms as a byproduct of various biological processes and …
Acetaldehyde | CH3CHO | CID 177 - PubChem
Acetaldehyde is the aldehyde formed from acetic acid by reduction of the carboxy group. It is the most abundant carcinogen in tobacco smoke.
Acetaldehyde: Properties, Reactions And Uses
Aug 8, 2024 · Acetaldehyde, also known as ethanal, is an organic chemical compound with the formula CH3CHO. It is a volatile, low-boiling, and highly flammable liquid characterized by its …
Acetaldehyde - an overview | ScienceDirect Topics
Acetaldehyde occurs naturally in coffee, bread, and ripe fruit and is produced by plants and is manufactured on a large scale in industry. It is also produced by the partial oxidation of ethanol.
Acetaldehyde: Properties, Risks, Safety, and Industrial ...
Explore acetaldehyde’s risks, safety protocols, and industrial applications in this in-depth guide. Get the essential knowledge you need!
Alcohol and Cancer Risk Fact Sheet - NCI
A fact sheet that summarizes the evidence linking alcohol consumption to the risk of various cancers. Includes information about factors that affect the risk of alcohol-associated cancers.
ACETALDEHYDE | CAMEO Chemicals | NOAA
Reactivity Profile ACETALDEHYDE undergoes a vigorously exothermic condensation reaction in contact with strong acids, bases or traces of metals.