2,6-DINITROPHENOL

2,6-DINITROPHENOL Basic information
Product Name:2,6-DINITROPHENOL
Synonyms:BETA-DINITROPHENOL;AURORA 6895;AKOS BBS-00008120;2,6-DINITROPHENOL;2,6-Dinitrophenol,wetted with not less than 15% water,by mass;2,6-Dinitrofenol;2,6-dinitro-pheno;2,6-dnp
CAS:573-56-8
MF:C6H4N2O5
MW:184.11
EINECS:209-357-9
Product Categories:Nitro;Aromatic Phenols;Phenol&Thiophenol&Mercaptan;Analytical Chemistry;Indicator (pH);pH Indicators
Mol File:573-56-8.mol
2,6-DINITROPHENOL Structure
2,6-DINITROPHENOL Chemical Properties
Melting point 61-63 °C(lit.)
Boiling point 318.03°C (rough estimate)
density 1.7195 (rough estimate)
vapor density 6.35 (vs air)
refractive index 1.4738 (estimate)
solubility Sparingly soluble in water; soluble in ethanol, chloroform, ether
pka3.69, 3.7, 3.5(at 25℃)
form crystals
color Yellowish
PH RangeColorless (1.7) to yellow (4.4)
Water Solubility 314.9mg/L(15 ºC)
Merck 14,3282
BRN 1913410
Stability:Light Sensitive, Possibly Shock Sensitive
Major ApplicationEnergetic materials, battery, lubricants, curing agents for epoxy resins, fungicidal, herbicidal, food storage, drugs
CAS DataBase Reference573-56-8(CAS DataBase Reference)
EPA Substance Registry System2,6-Dinitrophenol (573-56-8)
Safety Information
Hazard Codes T,N
Risk Statements 23/24/25-33-51/53-50/53
Safety Statements 28-37-45-61-36/37
RIDADR UN 1320 4.1/PG 1
WGK Germany 3
RTECS SL2975000
HazardClass 4.1
PackingGroup I
HS Code 29089990
Hazardous Substances Data573-56-8(Hazardous Substances Data)
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2,6-DINITROPHENOL Usage And Synthesis
Chemical PropertiesLight yellow crystalline
Uses2,6-Dinitrophenol is an aromatic nitrophenol.
DefinitionChEBI: 2,6-dinitrophenol is a dinitrophenol.
General DescriptionYellow crystalline solid with a sweet musty odor. Sinks and mixes slowly with water.
Air & Water ReactionsMixes slowly with water.
Reactivity Profile2,6-DINITROPHENOL can detonate or explode when heated under confinement [USCG, 1999]. Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases.
Health HazardINHALATION, INGESTION AND SKIN ABSORPTION: Headache, anorexia, nausea, vomiting, abdominal pain, diarrhea, fever, pain in chest, difficult breathing, profuse sweating and thirst, dizziness and fatigue. SKIN: Discoloration and irritation. Corrosive to skin.
Purification MethodsCrystallise it from H2O, aqueous EtOH, *C6H6/cyclohexane, or *C6H6/pet ether (b 60-80o, 1:1). [Beilstein 6 III 867, 6 IV 1383.]
METHYL 3,5-DINITRO-4-HYDROXYBENZOATE 3,5-DINITRO-4-HYDROXYBENZALDEHYDE PICRIC ACID 3,5-DINITRO-4-HYDROXYBENZOIC ACID AKOS 215-39 3,5-DINITRO-4-HYDROXYPHENYLPROPIONIC ACID HYDRAZIDE 4-CHLORO-2,6-DINITROPHENOL 4-TERT-BUTYL-2,6-DINITROPHENOL 97%,4-TERT-BUTYL-2,6-DINITROPHENOL 99+% 9,9'-BIFLUORENYLIDENE PICRATE 3-(4-HYDROXY-3,5-DINITROPHENYL)PROPANOIC ACID AC-3,5-DINITRO-TYR-OET 2,3,6-TRINITROPHENOL 3,5-DINITRO-4-HYDROXYPHENYLACETIC ACID N-Acetyl-3,5-dinitro-L-tyrosine MELAMINE PICRATE (+/-)-ANABASINE DIPICRATE 2,6-Dinitro-p-cresol 3,5-DINITRO-L-TYROSINE MONOHYDRATE

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.