2,6-dimethyl benzoic acid

benzoic acid, 2,6-dimethyl-

CAS: 632-46-2 C9 H10 O2 MW: 150.17710000

Identification

Name2,6-dimethyl benzoic acid
IUPAC2,6-dimethylbenzoic acid
CAS Number632-46-2
EINECS211-177-0
FDA UNIISearch
Molecular FormulaC9 H10 O2
Molecular Weight150.17710000
MDL NumberMFCD00002483
Nikkaji NumberJ83.361D
Beilstein1863791
XlogP32.20 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 116.00 °C. @ 760.00 mm Hg
Boiling Point 274.50 °C. @ 760.00 mm Hg
Flash Point 259.00 °F. TCC ( 126.10 °C. ) (est)
logP (o/w) 2.210
Soluble in water, 981.7 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityintraperitoneal-mouse LD50 178 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 2,6-dimethyl benzoic acid usage levels up tonot for fragrance use.
Recommendation for 2,6-dimethyl benzoic acid flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

horsetail water horsetail

Synonyms

benzoic acid, 2,6-dimethyl- 2,6- dimethylbenzoic acid m- xylene-2-carboxylic acid PubMed: Unique stepwise substitution reaction of a mono(guanidinate)tetraplatinum complex with amidines, giving mono(amidinate)tetraplatinum complexes through mixed-ligand intermediate complexes. PubMed: Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. PubMed: Five new compounds from Dendrobium crystallinum. PubMed: JBIR-26, a novel natural compound from Streptomyces sp. AK-AH76, regulates mammalian circadian clock. PubMed: [Studies on antibacterial activities of secondary metabolites from fungus Cephalosporium sp. AL031]. PubMed: Steric inhibition of resonance: a revision and quantitative estimation on the basis of aromatic carboxylic acids