2-methyl-1-naphthol

1-naphthalenol, 2-methyl- (9CI)

CAS: 7469-77-4 C11 H10 O MW: 158.19990000

Identification

Name2-methyl-1-naphthol
IUPAC2-methylnaphthalen-1-ol
CAS Number7469-77-4
EINECS231-265-2
FDA UNIICOU5JQ433I
Molecular FormulaC11 H10 O
Molecular Weight158.19990000
MDL NumberMFCD00003964
Nikkaji NumberJ130.656A

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 304.30 °C. @ 760.00 mm Hg (est)
Flash Point 297.00 °F. TCC ( 147.10 °C. ) (est)
logP (o/w) 3.170 (est)
Soluble in water, 457 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Useshair dyeing agents

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
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

Categoryhair dyeing agents
Recommendation for 2-methyl-1-naphthol usage levels up tonot for fragrance use.
Recommendation for 2-methyl-1-naphthol flavor usage levels up tonot for flavor use.

BOC Sciences

Best of Chemicals Supplier

Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...

View All Website 1-631-485-4226 account@bocsci.com

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

2- methyl-alpha-naphthol 2- methylnaphthalen-1-ol 1- naphthalenol, 2-methyl- 1- naphthalenol, 2-methyl- (9CI) 1- naphthol, 2-methyl- (8CI) PubMed: Selective synthesis of vitamin K3 over mesoporous NbSBA-15 catalysts synthesized by an efficient hydrothermal method. PubMed: Mechanistic insights into oxidation of 2-methyl-1-naphthol with dioxygen: autoxidation or a spin-forbidden reaction? PubMed: Synthesis and biological activity of tetralone abscisic acid analogues. PubMed: Purification and properties of a quinone-dependent p-nitrophenylphosphatase from Clostridium sticklandii. PubMed: Antibacterial properties of 4-amino-2-methyl-1-naphthol hydrochloride.