Testing Status of Agents at NTP
CAS Registry Number: 91-22-5
Selected information from two of the National Library of Medicine's databases: ChemIDPlus1 and HSDB2.
Names (NTP)
- Quinoline
- 1-AZANAPHTHALENE
- BENZOPYRIDINE
- LEUKOL
Structure
Chemical Properties2
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Uses2
- Manuf dyes; prepn hydroxyquinoline sulfate, q.v., niacin. As preservative for anatomical specimens. Solvent for resins abd terpenes.
- Chem int for 8-hydroxyquinoline, a fungistat; chem int for pharmaceuticals-e.g., antiinfectives; corrosion inhibitor
- Used as ... a decarboxylation reagent.
- Used in the manufacture of ... paints.
- Therap cat: antimalarial
- Manufacture of copper-8-hydroxyquinolate; flavoring
- The main application of quinoline is the production of 8-quinolinol, which is obtained by alkali fusion of quinoline-8-sulfonic acid. Quinoline can be used to produce methine dyes and nicotinic acid. Quinoline alone, or as a mixture with isoquinoline and quinoline homologues, is an excellent solvent and extractor, especially for polycyclic aromatic compounds.
Superlist Classes1
- Reportable Quantity (RQ) = 5000 lb
Notes (Sources: NTP,HSDB,RTECS,MESH)1
- None found
Other Registry Numbers1
- 20214-07-7
Synonyms (Sources: NTP, HSDB,RTECS,MESH)1
- B-500
- B 500
- AI3-01241
- 1-Azanaphthalene
- 1-Benzazine
- Benzopyridine
- Benzo(b)pyridine
- Chinoleine
- Chinoline
- HSDB 121
- Leucol
- Leukol
- Quinolin
- USAF EK-218
Links to Additional Information1
- PubMed Cancer
- CCRIS
- DART
- EINECS
- EMIC
- GENETOX
- HSDB
- IRIS
- ITER
- PubMed
- MeSH
- PubMed Toxicology
- TOXLINE
- TOXMAP
- TRI2000
- TRI2001
- TRI2002
- TRI95
- TRI96
- TRI97
- TRI98
- TRI99
- PubChem
- TRI2003
- TRI2004
- TRI2005
Footnotes
1 Source: the National Library of Medicine's ChemIDPlus, 10/28/2007.
2 Source: the National Library of Medicine's Hazardous Substance Database, 10/28/2007.
Web page last updated on May 14, 2008