China (Mainland)
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3-Methylindole_ CAS NO.83-34-1
- Min.Order: 1 Kilogram
- Payment Terms: L/C,D/A,D/P,T/T,MoneyGram,Other
- 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 |
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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 |