5-METHOXYINDOLE

PRODUCT IDENTIFICATION

CAS NO 1006-94-6

5-METHOXYINDOLE

EINECS NO.

213-745-3

FORMULA C9H9NO
MOL WT. 147.18

H.S. CODE

2933.99.7900

TOXICITY

 

SYNONYMS

5-Methoxy-2,3-benzopyrrole; Methoxy-5 indole; Indol-5-yl methyl ethe;

5-Methoxy-1H-indole; 5-Methoxyindole;

SMILES c12c(ccc(c1)OC)[nH]cc2

CLASSIFICATION 

 

EXTRA NOTES

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE

white to grey crystalline powder 

MELTING POINT

56 - 58 C

BOILING POINT 176 - 178 C at 17 mmHg
SPECIFIC GRAVITY  

SOLUBILITY IN WATER

1,360 mg/l
pH  
VAPOR DENSITY  

REFRACTIVE INDEX

 

AUTOIGNITION

 

NFPA RATINGS Health: 1; Flammability: 0; Reactivity: 0
FLASH POINT

 

FLASH POINT

 

STABILITY Stable under normal conditions.

EXTERNAL LINKS & GENERAL DESCRIPTION

Google Scholar Search - 5-Methoxyindole

Drug Information Portal (U.S. National Library of Medicine) - 5-Methoxyindole

PubChem Compound Summary - 5-Methoxyindole

KEGG (Kyoto Encyclopedia of Genes and Genomes) - 5-Methoxyindole

http://www.ebi.ac.uk/ - 5-Methoxyindole

http://www.ncbi.nlm.nih.gov/ - 5-Methoxyindole

Material Safety Data Sheet

http://toxnet.nlm.nih.gov/
Hazardous Substances Data Bank - 5-Methoxyindole

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. 

SALES SPECIFICATION

APPEARANCE

white to grey crystalline powder

PURITY (HPLC)

98.0% min

LOSS ON DRYING

0.2% max

MELTING POINT

51 - 58 C

TRANSPORTATION
PACKING  
HAZARD CLASS Not regulated
UN NO.  
SAFETY INFORMATION

HAZARD OVERVIEW

May cause eye, skin, and respiratory tract irritation.

GHS

 

SIGNAL WORD Warning

PICTOGRAMS

HAZARD STATEMENTS

H315-H319-H335

P STATEMENTS

P261-P305 + P351 + P338

EC DIRECTIVES

 

HAZARD CODES

RISK PHRASES

36/37/38

SAFETY PHRASES

26-36

PRICE INFORMATION