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157384

Sigma-Aldrich

Phenanthridine

98%

Synonym(s):

Benzo[c]quinoline

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About This Item

Empirical Formula (Hill Notation):
C13H9N
CAS Number:
Molecular Weight:
179.22
Beilstein:
120204
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

98%

form

powder

bp

349 °C/769 mmHg (lit.)

mp

104-107 °C (lit.)

SMILES string

c1ccc2c(c1)cnc3ccccc23

InChI

1S/C13H9N/c1-2-6-11-10(5-1)9-14-13-8-4-3-7-12(11)13/h1-9H

InChI key

RDOWQLZANAYVLL-UHFFFAOYSA-N

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Application

  • Used in the study of ecotoxicity.
  • Used in rotational spectroscopic investigations and radio astronomical searches.
  • Used as a dye in biological and chemical sensors.

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The TRPA1 channel can be considered as a key biological sensor to irritant chemicals. In this paper, the discovery of 11H-dibenz[b,e]azepines (morphanthridines) and dibenz[b,f][1,4]oxazepines is described as extremely potent agonists of the TRPA1 receptor. This has led to the discovery

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