CAS 6034-46-4
:(2S)-2-(Acetyloxy)propanoic acid
Description:
(2S)-2-(Acetyloxy)propanoic acid, commonly known as acetylsalicylic acid or aspirin, is a colorless to white crystalline solid with a characteristic odor. It is classified as a non-steroidal anti-inflammatory drug (NSAID) and is widely used for its analgesic, antipyretic, and anti-inflammatory properties. The compound features a carboxylic acid functional group and an acetoxy group, which contribute to its reactivity and biological activity. It is soluble in organic solvents like ethanol and acetone but has limited solubility in water. The substance exhibits a melting point that is typically in the range of room temperature, making it stable under normal conditions. Its mechanism of action primarily involves the inhibition of cyclooxygenase enzymes, leading to a decrease in the synthesis of prostaglandins, which are mediators of pain and inflammation. Additionally, it is known for its antiplatelet effects, making it useful in cardiovascular disease prevention. Proper storage away from moisture and light is recommended to maintain its efficacy and stability.
Formula:C5H8O4
InChI:InChI=1/C5H8O4/c1-3(5(7)8)9-4(2)6/h3H,1-2H3,(H,7,8)/t3-/m0/s1
InChI key:InChIKey=WTLNOANVTIKPEE-VKHMYHEASA-N
SMILES:[C@@H](OC(C)=O)(C(O)=O)C
Synonyms:- (+)-Lactic acid acetate
- (+)-α-Acetoxypropionic acid
- (-)-O-Acetyl-<span class="text-smallcaps">L</span>-lactic acid
- (2R)-2-(acetyloxy)propanoic acid
- (2S)-2-(acetyloxy)propanoic acid
- (2S)-2-Acetoxypropanoic acid
- (2S)-2-Acetyloxypropanoic acid
- (2S)-2-Acetyloxypropionic acid
- (2S)-Acetoxypropionic acid
- (S)-(+)-2-Acetoxypropanoic acid
- (S)-(-)-2-Acetoxypropionic acid
- (S)-O-Acetyllactic acid
- 2(S)-Acetoxypropionic acid
- <span class="text-smallcaps">L</span>-(+)-O-Acetylactic acid
- <span class="text-smallcaps">L</span>-Lactic acid acetate
- Lactic acid, acetate, <span class="text-smallcaps">L</span>-
- O-Acetyl-(S)-lactic acid
- Propanoic acid, 2-(acetyloxy)-, (2S)-
- Propanoic acid, 2-(acetyloxy)-, (S)-
- α-(Acetyloxy)-<span class="text-smallcaps">L</span>-propionic acid
- Lactic acid, acetate, L-
- (-)-O-ACETYL-L-LACTIC AICD
- [S,(-)]-2-(Acetyloxy)propionic acid
- (S)-ACETYLLACTIC ACID
- (-)-2-O-Acetyl-L-lactic acid
- (S)-ALPHA-ACETOXYPROPIONIC ACID
- L-Lactic acid acetate
- (S)-A-2-ACETOXYPROPIONIC ACID
- See more synonyms
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Found 7 products.
(S)-2-Acetoxypropanoic acid
CAS:Formula:C5H8O4Purity:96%Color and Shape:LiquidMolecular weight:132.1146(S)-(-)-2-Acetoxypropionic acid
CAS:(S)-(-)-2-Acetoxypropionic acidPurity:98%Color and Shape:Colourless To Pale Yellow LiquidMolecular weight:132.11g/mol(-)-O-ACETYL-L-LACTIC ACID
CAS:Purity:97.0%Color and Shape:Liquid, ClearMolecular weight:132.11500549316406(S)-(-)-2-Acetoxypropionic Acid
CAS:Formula:C5H8O4Purity:>98.0%(T)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:132.12(S)-2-Acetoxypropanoic Acid-d3
CAS:Controlled ProductFormula:C5D3H5O4Color and Shape:NeatMolecular weight:135.133(S)-2-Acetoxy-propionic acid
CAS:<p>(S)-2-Acetoxy-propionic acid is a hexyl, enantiopure, and biologically active chemical. It is a pheromone that is secreted by the streptomycetaceae bacterium as part of its mating process. It has been shown to have an inhibitory effect on stingless bees, which are native to Central America and South America. (S)-2-Acetoxy-propionic acid has been found in the mandibular glands of these bees and is believed to play a role in their behavior. This chemical can be synthesized from propionic acid and acetaldehyde or from lactic acid and acetaldehyde. It is also possible to produce it from 2-bromopropanoic acid through the tripropionate pathway. The chemical was first isolated in 1957 by Takaichi Yamashita, who named it for its ability to inhibit bee stings when applied externally. (S)-2-Acetoxy</p>Formula:C5H8O4Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:132.11 g/mol






