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HSDB 6304

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HSDB 6304 - Names and Identifiers

Name 2,5-Dinitrophenol
Synonyms 2,5-DNP
HSDB 6304
NSC 90441
CCRIS 3103
BRN 1913411
2,5-Dinitrofenol
2,5-dinitro-pheno
gamma-dinitro-pheno
gamma-Dinitrophenol
Phenol, 2,5-dinitro-
Phenol, gamma-dinitro-
2,5-Dinitrofenol [Czech]
2,5-Dinitrophenol ( betta )
CAS 329-71-5
EINECS 206-348-1
InChI InChI=1/C6H4N2O5/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3,9H

HSDB 6304 - Physico-chemical Properties

Molecular FormulaC6H4N2O5
Molar Mass184.11
Density1.7195 (rough estimate)
Melting Point103-106°C(lit.)
Boling Point318.03°C (rough estimate)
Flash Point141.5°C
Solubility Solubility Sparingly soluble in water; soluble in ethanol, ether
Vapor Presure0.000346mmHg at 25°C
ColorYellowish needles
Merck14,3281
BRN1913411
pKa5.21, 5.1, 5.0(at 25℃)
Refractive Index1.4738 (estimate)
Physical and Chemical PropertiesYellow needle-like crystals. Melting point 108 °c. Soluble in ether, hot ethanol and benzene, water-soluble. Can be volatilized with water vapor.

HSDB 6304 - Reference Information

pH indicator color change ph range 4(colourless)-5.8(yellow)
main applications liquid crystal films, electrophotographic materials, adhesives, inks, lubricants, preservation of cut flowers, food storage, materials for evaluating Dental cariesactivity
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
use for organic synthesis. Used as an indicator in chemical analysis, the 70% ethanol solution is prepared into a 0.05-0.1% solution or its saturated aqueous solution is used as an indicator, and the pH color change range is 4.0 (colorless)-5.8 (yellow).
production method obtained by nitration of m-nitrophenol. Heat 40% nitric acid to 40 ℃, slowly add m-nitrophenol, and add it at 40-60 ℃ for about 3 hours. Then heat at 50-70 ℃ for 1h, after cooling, pour the dilute acid solution, crush the solid, wash the acid with ice water, and filter dry. The resulting product was dissolved in cold ethanol, where the insoluble substance was 2, 5-dinitrophenol.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 15:16:49
HSDB 6304
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HSDB 6304
CCRIS 505
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