missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Indole, 99%
CAS: 120-72-9 | C8H7N | 117.151 g/mol
$83.95 - $939.58
Chemical Identifiers
| CAS | 120-72-9 |
|---|---|
| Molecular Formula | C8H7N |
| Molecular Weight (g/mol) | 117.151 |
| MDL Number | MFCD00005607 |
| InChI Key | SIKJAQJRHWYJAI-UHFFFAOYSA-N |
| Synonym | indole, indol, 2,3-benzopyrrole, 1-benzazole, ketole, 1-azaindene, benzopyrrole, 2,3-benzopyrole, caswell no. 498b, indol german |
| PubChem CID | 798 |
| ChEBI | CHEBI:16881 |
| IUPAC Name | 1H-indole |
| SMILES | C1=CC=C2C(=C1)C=CN2 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|
AAA1442718
|
Thermo Scientific Chemicals
A1442718 |
50 g |
Each for $83.95
|
|
|||||
|
AAA1442730
|
Thermo Scientific Chemicals
A1442730 |
250 g |
Each for $288.14
|
|
|||||
|
AAA144270B
|
Thermo Scientific Chemicals
A144270B |
1000 g |
Each for $939.58
|
|
|||||
Description
Indole is used in the preparation of gramine, which is obtained by Mannich reaction dimethylamine and formaldehyde. It is used as a starting material for the preparation of oxindole and indole-3-carboxaldehyde. In Diels-Alder reaction, it acts as dienophile and reacts with 2-aminofuran to get strychnine. It is the active component of jasmine oil, neroli oil and orange-blossom oil used in the perfume industry. Further, it is involved in the preparation of synthetic jasmine oil.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsIndole is used in the preparation of gramine, which is obtained by Mannich reaction dimethylamine and formaldehyde. It is used as a starting material for the preparation of oxindole and indole-3-carboxaldehyde. In Diels-Alder reaction, it acts as dienophile and reacts with 2-aminofuran to get strychnine. It is the active component of jasmine oil, neroli oil and orange-blossom oil used in the perfume industry. Further, it is involved in the preparation of synthetic jasmine oil.
Solubility
Soluble in methanol and water.
Notes
Light and air sensitive. Store in a cool place. Incompatible with strong oxidizing agents, iron and iron salts. Keep the container tightly closed in a dry and well-ventilated place.
Chemical Identifiers
| 120-72-9 | |
| 117.151 | |
| SIKJAQJRHWYJAI-UHFFFAOYSA-N | |
| 798 | |
| 1H-indole |
| C8H7N | |
| MFCD00005607 | |
| indole, indol, 2,3-benzopyrrole, 1-benzazole, ketole, 1-azaindene, benzopyrrole, 2,3-benzopyrole, caswell no. 498b, indol germanShow More | |
| CHEBI:16881 | |
| C1=CC=C2C(=C1)C=CN2 |
Specifications
| 120-72-9 | |
| 1.22 | |
| 253°C to 254°C | |
| Unpleasant | |
| MFCD00005607 | |
| UN2811 | |
| Light sensitive | |
| indole, indol, 2,3-benzopyrrole, 1-benzazole, ketole, 1-azaindene, benzopyrrole, 2,3-benzopyrole, caswell no. 498b, indol german | |
| SIKJAQJRHWYJAI-UHFFFAOYSA-N | |
| 1H-indole | |
| 798 | |
| 117.15 | |
| Indole |
| 50°C to 54°C | |
| 6 | |
| 121°C (249°F) | |
| C8H7N | |
| 50 g | |
| 107693 | |
| 14,4963 | |
| Soluble in methanol and water. | |
| C1=CC=C2C(=C1)C=CN2 | |
| 117.151 | |
| CHEBI:16881 | |
| 99% |
Safety and Handling
GHS H Statement
H311-H318-H302
Toxic in contact with skin.
Causes serious eye damage.
Harmful if swallowed.
P261-P264b-P270-P272-P280-P301+P312-P302+P352-P305+P351+P338-P310-P312-P330-P333+P313-P361-P363-P501c
H302-H311-H317-H318
DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.
EINECSNumber : 204-420-7
RTECSNumber : NL2450000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only