4-(2,4-DINITROANILI...

4-(2,4-DINITROANILINO)PHENOL
4-(2,4-DINITROANILINO)PHENOL
4-(2,4-DINITROANILINO)PHENOL

4-(2,4-DINITROANILINO)PHENOL

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4-(2,4-DINITROANILINO)PHENOL 119-15-3 C12H9N3O5

Quick Details

  • Appearance:reddish-brown solid
  • Application:119-15-3
  • PackAge:As requested
  • ProductionCapacity:300|Metric Ton|Day
  • Storage:keep in dry and ventilated
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4-(2,4-DINITROANILINO)PHENOL Basic information
Product Name: 4-(2,4-DINITROANILINO)PHENOL
Synonyms: LABOTEST-BB LT01487957;DISPERSE YELLOW 1;2,4-DINITRO-4'-HYDROXYDIPHENYLAMINE;4-[(2',4'-DINITROPHENYL)AMINO]-PHENOL;4-(2,4-DINITROANILINO)PHENOL;P-(2,4-DINITROANILINO)PHENOL;TIMTEC-BB SBB001098;2,4-Dinitro-p-hydroxydiphenylamine
CAS: 119-15-3
MF: C12H9N3O5
MW: 275.22
EINECS: 204-300-4
Product Categories:  
Mol File: 119-15-3.mol
4-(2,4-DINITROANILINO)PHENOL Structure
 
4-(2,4-DINITROANILINO)PHENOL Chemical Properties
mp  191 °C (dec.)(lit.)
CAS DataBase Reference 119-15-3(CAS DataBase Reference)
 
Safety Information
Hazard Codes  F,Xi
Risk Statements  11-36/37/38
Safety Statements  16-26-33-36/37/39
RIDADR  UN 1325 4.1/PG 2
WGK Germany  2
RTECS  SL3070000
HazardClass  4.1
PackingGroup  III
 
4-(2,4-DINITROANILINO)PHENOL Usage And Synthesis
General Description Reddish-brown solid.
Air & Water Reactions Insoluble in water.
Reactivity Profile 4-(2,4-DINITROANILINO)PHENOL is an organonitrate/phenol. Organonitrate compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups. 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.
Fire Hazard Flash point data for 4-(2,4-DINITROANILINO)PHENOL are not available, however, 4-(2,4-DINITROANILINO)PHENOL is probably combustible.

 

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