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3-Methylindole_ CAS NO.83-34-1

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

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Product Details

Keywords

  • 3-Methylindole
  • 83-34-1
  • 3-Methylindole

Quick Details

  • ProName: 3-Methylindole_
  • CasNo: 83-34-1
  • Molecular Formula: C9H9N
  • Appearance: slightly brown platelets
  • Application: For Organic Synthesis use
  • DeliveryTime: PROMPT
  • PackAge: IN 25kg drums
  • Port: SHANGHAI
  • ProductionCapacity: 10 Metric Ton/Month
  • Purity: 99.0%
  • Storage: In Room Temperature
  • Transportation: As Per MSDS
  • LimitNum: 1 Kilogram
  • Heavy metal: N/A
  • Grade: Industrial Grade,Food Grade,Pharma Gra...
  • Transporttation: N/A

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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