CAS 17432-38-1
:PENTAMETHYLBENZALDEHYDE
Description:
Pentamethylbenzaldehyde, with the CAS number 17432-38-1, is an aromatic aldehyde characterized by its distinct structure, which features a benzene ring substituted with five methyl groups and an aldehyde functional group. This compound typically appears as a colorless to pale yellow liquid with a strong, sweet, and floral odor, making it valuable in the fragrance industry. Its molecular formula is C12H16O, and it has a relatively low boiling point, which contributes to its volatility. Pentamethylbenzaldehyde is known for its stability under normal conditions but may undergo oxidation or polymerization when exposed to strong oxidizing agents. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. Due to its unique scent profile, it is often used in perfumes, cosmetics, and flavoring agents. Safety data indicates that, while it may cause irritation upon contact with skin or eyes, it is generally considered to have low toxicity when handled properly.
Formula:C12H16O
InChI:InChI=1/C12H16O/c1-7-8(2)10(4)12(6-13)11(5)9(7)3/h6H,1-5H3
SMILES:Cc1c(C)c(C)c(C=O)c(C)c1C
Synonyms:- 2,3,4,5,6-Pentamethyl-Benzaldehyde
- 2,3,4,5,6-Pentabenzaldehyde
- Pentamethylbenzaldehyde 98%
- Pentamethylbenzaldehyde 97+%
- 2,3,4,5,6-Pentamethylbenzaldehyde, GC 97%
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Found 5 products.
Pentamethylbenzaldehyde
CAS:Formula:C12H16OPurity:>96.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:176.26Benzaldehyde, 2,3,4,5,6-pentamethyl-
CAS:Formula:C12H16OPurity:98%Color and Shape:SolidMolecular weight:176.25482,3,4,5,6-Pentamethylbenzaldehyde
CAS:<p>2,3,4,5,6-Pentamethylbenzaldehyde is an aromatic nitro compound that can be used as a precursor in the synthesis of other compounds. The reaction of 2,3,4,5,6-pentamethylbenzaldehyde with hydrogen chloride or acidic hydrolysis yields two compounds: 2-chloro-3-(2-nitrophenyl)propene and 5-(2-nitrophenyl)pentanal. These two compounds are activated methylene compounds that can be converted to other organic compounds with the use of a cocatalyst. It has been shown to inhibit human ovarian carcinoma cells and stabilize cardiac arrhythmias.</p>Formula:C12H16OPurity:Min. 95%Color and Shape:PowderMolecular weight:176.26 g/mol




