2-METHYLINDOLE

PRODUCT IDENTIFICATION

CAS NO. 95-20-5

2-METHYLINDOLE

EINECS NO. 202-398-3
FORMULA C9H9N
MOL WT. 131.18
H.S. CODE 2933.99.9700
TOXICITY  
SYNONYMS 2-Methyl-1H-indole; Methylketol;
SMILES c12c([nH]c(c1)C)cccc2

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE pale yellow melt
MELTING POINT

58 ~ 60 C

BOILING POINT 273 C
DENSITY 1.07
SOLUBILITY IN WATER Insoluble

pH

 

AUTOIGNITION  
VAPOR DENSITY  
NFPA RATINGS Health: 2; Flammability: 1 ; Reactivity: 0
FLASH POINT

141 C

STABILITY Stable under ordinary conditions. Light sensitive

EXTERNAL LINKS & GENERAL DESCRIPTION

USA.gov - 2-Methylindole

Wikipedia Linking - 2-Methylindole

Google Scholar Search - 2-Methylindole

U.S. National Library of Medicine - 2-Methylindole

PubChem Compound Summary - 2-Methylindole

NCBI (http://www.ncbi.nlm.nih.gov/) -  2-Methylindole

Material Safety Data Sheet - 2-Methylindole

Human Metabolome Database - 2-Methylindole

EPA - Substance Registry Services - 2-Methylindole

Local:
Indole, benzopyrrole, is a yellow crystalline powder with unpleasant aroma. It has the pyrrole ring (five-membered unsaturated ring structure composed of four carbon atoms and one nitrogen atom) which is fused to benzene ring. There are tautomerer called indolenine (unsubstituted 3H-indole) and structural isomer, isoindole. But they are unstable. Indole occurs in some plants or in coal tar, and is formed in the intestine during putrefaction and by certain cultures of bacteria. it is commercially synthesized from phenylhydrazine and pyruvic acid. Indole structure is a motif in nature. Prominent examples include tryptophan (aromatic side chain amino acid), serotonin (neurotransmitter), auxin (plant growth hormone), and indigo (plant colorant). One more interesting point is all these compounds have functional branches at 3 position. Indole is used in perfumery and in preparing tryptophan, one of the 20 amino acids commonly found in animal proteins. It has important application in the industry of plant growth. It is used to prepare indoleacetic acid (auxin) and other plant growth substances which help the development of roots in plant. It is used to make selective herbicides. Indole and its derivatives are widely used in making perfumes, dyes, agrochemicals and medicines. 2-Methylindole is used as an intermediate for the synthesis of dyes, pigments, optical brighteners and pharmaceuticals.

SALES SPECIFICATION

APPEARANCE

pale yellow melt
ASSAY 98.0% min
MELTING POINT

58 - 60 C

TRANSPORTATION
PACKING  
HAZARD CLASS Not regulated
UN NO.  
SAFETY INFORMATION

HAZARD OVERVIEW

GHS (Globally Harmonised System) Classification: Serious eye damage. Hazard statements: Harmful if swallowed. Causes skin irritation. Causes serious eye damage. May cause respiratory irritation.

GHS

 

SIGNAL WORD Danger

PICTOGRAMS

PICTOGRAM_GHS05_corrosion.jpg

HAZARD STATEMENTS

H302-H315-H318-H335

P STATEMENTS

P280-P305 + P351 + P338

EC DIRECTIVES

 

HAZARD CODES

RISK PHRASES

41

SAFETY PHRASES

26-39

PRICE INFORMATION