Dinonyl phthalate
Dinonyl phthalate Basic information
- Product Name:
- Dinonyl phthalate
- Synonyms:
-
- Dinonyl Phthalate (mixture of branched chain isomers)
- Bisoflex 91
- Bisoflex DNP
- bisoflex91
- bisoflexdnp
- bisolflex91
- Ceneg
- 1,2-benzenediacarboxylicaciddinonylester
- CAS:
- 84-76-4
- MF:
- C26H42O4
- MW:
- 418.61
- EINECS:
- 201-560-0
- Product Categories:
-
- important and primary plasticizer
- Functional Materials
- Phthalates (Plasticizer)
- Plasticizer
- Gas Chromatography
- Packed GC
- Stationary Phases
- Mol File:
- 84-76-4.mol
Dinonyl phthalate Chemical Properties
- Melting point:
- -33.15°C
- Boiling point:
- 279-287 °C(lit.)
- Density
- 0.98 g/mL at 20 °C(lit.)
- refractive index
- n20/D 1.486
- Flash point:
- 216°C
- form
- Oily Liquid
- color
- Clear yellow-brown
- Water Solubility
- <1 g/L (20 ºC)
- BRN
- 1916263
- Dielectric constant
- 4.5(45℃)
- InChIKey
- DROMNWUQASBTFM-UHFFFAOYSA-N
- CAS DataBase Reference
- 84-76-4(CAS DataBase Reference)
- NIST Chemistry Reference
- 1,2-Benzenedicarboxylic acid, dinonyl ester(84-76-4)
- EPA Substance Registry System
- Dinonyl phthalate (84-76-4)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 1
- RTECS
- TI1800000
- TSCA
- Yes
- HS Code
- 29173300
- Hazardous Substances Data
- 84-76-4(Hazardous Substances Data)
MSDS
- Language:English Provider:Dinonyl phthalate
- Language:English Provider:ALFA
Dinonyl phthalate Usage And Synthesis
Chemical Properties
clear yellow-brown oily liquid
Uses
Dinonyl Phthalate is a Phthalate derivative and an organic extract contaminant found in drinking water, which was shown to activate Nrf-2-Mediated Antioxidant response in human cell line.
General Description
Odorless colorless liquid.
Air & Water Reactions
Flammable. Hydrolyzed by strong mineral acids and strong alkalis.
Reactivity Profile
Dinonyl phthalate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Can generate electrostatic charges [Handling Chemicals Safely, 1980. p. 250].
Health Hazard
Moderately toxic by ingestion.
Purification Methods
Wash the ester with aqueous Na2CO3 then shake it with water. Ether is added to break the emulsion, and the solution is washed twice with water, and dried (CaCl2). After evaporating the ether, the residual liquid is distilled three times under reduced pressure. It is stored in a vacuum desiccator over P2O5. [Beilstein 9 IV 3183.]
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Dinonyl phthalate(84-76-4)Related Product Information
- DI-N-HEXYL PHTHALATE
- Tris(trimethylsilyl)phosphate
- Dicyclohexyl phthalate
- DI-N-PENTYL PHTHALATE-D4
- Benzyl benzoate
- Bis(2-ethylhexyl) phthalate
- Bis(2-methoxyethyl) phthalate
- 1,2-Benzenedicarboxylic acid di-C9-11-branched alkyl esters C10-rich
- Didecyl phthalate
- Benzyl butyl phthalate
- Dibutyl phthalate
- Dimethyl phthalate
- Dimethyl succinate
- Phthalic acid
- Diisononyl phthalate
- Diethyl phthalate
- Diallyl phthalate
- Potassium hydrogen phthalate