1-NITROANTHRAQUINONE
1-NITROANTHRAQUINONE Basic information
- Product Name:
- 1-NITROANTHRAQUINONE
- Synonyms:
-
- 1-NITROANTHRAQUINONE
- 1-Nitoanthrapuinone
- 1-Nitro-9,10-anthraquinone
- 1-Nitroanthraquinione
- 1-Nitroanthracene-9,10-dione 82-34-8 In stock factory 1-Nitroanthraquinone 82-34-8
- 1-Nitroanthracene-9,10-dione 82-34-8 1-Nitroanthraquinone 82-34-8
- 1-Nitroanthracene-9,10-dione 82-34-8 Manufacturer High quality Best price In stock factory 1-Nitroanthraquinone 82-34-8
- tetrafluorotitanium
- CAS:
- 82-34-8
- MF:
- C14H7NO4
- MW:
- 253.21
- EINECS:
- 201-413-0
- Product Categories:
-
- Anthraquinones
- Chloroanthraquine, etc.
- Intermediates of Dyes and Pigments
- Mol File:
- 82-34-8.mol
1-NITROANTHRAQUINONE Chemical Properties
- Melting point:
- 232.5~233.5℃
- Boiling point:
- 270~271℃(933Pa)
- Density
- 1.3146 (rough estimate)
- refractive index
- 1.4700 (estimate)
- Flash point:
- 243.3 ±18.5 ℃
- storage temp.
- Sealed in dry,Room Temperature
- Water Solubility
- Insoluble in water
- form
- powder to crystal
- color
- Light yellow to Brown
- CAS DataBase Reference
- 82-34-8(CAS DataBase Reference)
- EPA Substance Registry System
- 9,10-Anthracenedione, 1-nitro- (82-34-8)
Safety Information
- Risk Statements
- 20/21/22
- Safety Statements
- 22-36/37/39
- RTECS
- CB7940000
- HS Code
- 2914.69.9000
1-NITROANTHRAQUINONE Usage And Synthesis
Chemical Properties
Yellow needles from AcOH;yellow plates by sublimation; soluble in EtOH and Et2O; slightly soluble in EtOAc, benzene and CHCl3; insoluble in water.
Uses
1-Nitroanthraquinone is used in the manufacture of various dyes, pharmaceuticals and similar products, either directly or after reduction to l-aminoanthraquinone.
Synthesis Reference(s)
Tetrahedron Letters, 16, p. 1429, 1975 DOI: 10.1016/S0040-4039(00)72160-5
Hazard
Hepatotoxic; moderately toxic; may cause hepatocellular neoplasms, subcutaneous fibromas, subcutaneous hemangiosarcomas, and type II pneumocyte proliferation.
Synthesis
1-Nitroanthraquinone is prepared by nitration of
anthraquinone in nitric acid (danger of explosion!)
, sulfuric acid , organic
solvents , phosphoric acid , or hydrogen
fluoride .
Purification from organic solvents by addition
of bases, such as amines , alcoholates
, or hydrazine , or from water by
addition of sodium sulfite . 1-Nitroanthraquinone
is crystallized from nitric acid ,
from organic solvents, for example, nitrobenzene
, or from amides . The resulting
1-nitroanthraquinone may be finally purified by
high-temperature distillation , .
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