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ChemicalBook >> CAS DataBase List >>2,4-Dinitrophenol

2,4-Dinitrophenol suppliers

2,4-Dinitrophenol

CAS:
51-28-5
MF:
C6H4N2O5
MW:
184.11

Company Type

Properties

Melting point:
108-112 °C (lit.)
Boiling point:
318.03°C (rough estimate)
Density 
1,683 g/cm3
vapor density 
6.35 (vs air)
vapor pressure 
39(x 10-5 mmHg) at 20 °C (Schwarzenbach et al., 1988)
refractive index 
1.4738 (estimate)
Flash point:
11 °C
storage temp. 
2-8°C
solubility 
Solubility Sparingly soluble in water; soluble in ethanol, benzene
form 
crystals
pka
3.96(at 15℃)
color 
Light yellow
PH Range
2.8(colourless)-4.7(yellow)
Odor
Sweet, musty
Water Solubility 
0.6 g/100 mL (18 ºC)
Sensitive 
Light Sensitive
Merck 
14,3280
BRN 
1246142
Henry's Law Constant
5.70 x 10-8(atm?m3/mol) at 5 °C (average derived from six field experiments, Lüttke and Levsen, 1997)
Stability:
Stable. Combustible.
Major Application
Display device, recording materials, inks, paints, method for preserving food, method for gene expression profiling, treatment of parasitic diseases, neurological diseases, epilepsy, cancer, keratin materials, neoplasms, infectious diseases, neutropenia, detecting chromosome aberrations, bacteria in gastrointestinal track

Safety Information

Symbol(GHS) 
GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS06,GHS08,GHS09
Signal word 
Danger
Hazard statements 
H208-H300-H311+H331-H372-H400
Precautionary statements 
P210-P212-P230-P233-P280-P301+P310-P371+P380+P375-P501
Hazard Codes 
T,N,Xi,F
Risk Statements 
23/24/25-33-50-39/23/24/25-11-52/53-1
Safety Statements 
28-37-45-61-28A-36/37-16-7-35
RIDADR 
UN 1320 4.1/PG 1
WGK Germany 
3
RTECS 
SL2800000
TSCA 
Yes
HazardClass 
4.1
PackingGroup 
I
HS Code 
29089990
Toxicity
LD50 (subcutaneous) for rats 25 mg/kg (quoted, RTECS, 1985).

Use

The bacterial strain RB1, which is isolated by enrichment cultivation with 2,4-dinitrophenol, degrades this phenol into two aliphatic acids. One metabolite results from the release of the 2-nitro group as nitrile, with the production of aliphatic nitro compound, 3-nitroadipate. Then, the 3-nitro group is released from this metabolite as nitrile. The other metabolite is 4,6-dinitrohexanoic acid possessing two nitro groups from 2,4-dinitrophenol.

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