3-Methylindole_

3-Methylindole_

3-Methylindole_

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99.0%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram,Other

Keywords

3-Methylindole 83-34-1 3-Methylindole

Quick Details

  • Appearance:slightly brown platelets
  • Application:For Organic Synthesis use
  • PackAge:IN 25kg drums
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:In Room Temperature
  • Transportation:As Per MSDS

Superiority:

3-Methylindole Basic information
Product Name: 3-Methylindole
Synonyms: FEMA 3019;BETA-METHYLINDOLE;3-MI;3-METHYL-1H-INDOLE;3-METHYLINDOLE;SCATOLE;SKATOL;SKATOLE
CAS: 83-34-1
MF: C9H9N
MW: 131.17
EINECS: 201-471-7
Product Categories: IndoleDerivative;Pyrroles & Indoles;Indoles;Simple Indoles;Pyrroles & Indoles;Aromatics;Indole Derivatives;Heterocycle-Indole series
Mol File: 83-34-1.mol
3-Methylindole Structure

 

Details:

 
 
3-Methylindole Chemical Properties
mp  92-97 °C(lit.)
bp  265-266 °C(lit.)
FEMA  3019
Fp  132 °C
Sensitive  Light Sensitive
Merck  14,8560
BRN  111296
Stability: Stable, but light-sensistive. Stench! Incompatible with strong oxidizing agents, strong acids, acid ahydrides, acid chlorides. Combustible.
CAS DataBase Reference 83-34-1(CAS DataBase Reference)
NIST Chemistry Reference 1H-Indole, 3-methyl-(83-34-1)
EPA Substance Registry System 1H-Indole, 3-methyl-(83-34-1)
 
Safety Information
Hazard Codes  Xi,N
Risk Statements  36/37/38-51/53
Safety Statements  26-36-61
WGK Germany  2
RTECS  NM0350000
F  8-13
HS Code  29339920
Hazardous Substances Data 83-34-1(Hazardous Substances Data)
 
 
3-Methylindole Usage And Synthesis
Chemical Properties slightly brown platelets
Usage insect attractant
Usage A naturally abundant pneumotoxin, found primarily in mammalian feces providing its strong fecal odor. In lower concentrations however, the compound has a pleasent aroma, giving orange blossoms and ja smine their pleasing scent. It is often a component of commercial fragrances and perfumes.
Usage A highly fluorescent guanosine analogue, which in a dimethoxytrityl, phosphoramidite protected form, can be site-specifically inserted into oligonucleotides through a 35phosphodiester linkage using an automated DNA synthesizer

 

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