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1,5-Dinitronaphthalene

CAS No.
605-71-0
Chemical Name:
1,5-Dinitronaphthalene
Synonyms
1,5-Dinitrophthalene;1,5-Dinitroaphthalene;1,5-DINITRO NAPHTALENE;1,5-dinitro-naphthalen;LABOTEST-BB LT00436936;1,5-DINITRONAPHTHALENE;Naphthalene,1,5-dinitro-;1,5-Dinitronaphthalene98%;1.5-Dinitronaphthalene 10;1,5-Dinitronaphthalene, 97+%
CBNumber:
CB9853955
Molecular Formula:
C10H6N2O4
Molecular Weight:
218.17
MDL Number:
MFCD00003916
MOL File:
605-71-0.mol
MSDS File:
SDS
Last updated:2024-04-19 20:05:26

1,5-Dinitronaphthalene Properties

Melting point 214 °C
Boiling point 358.84°C (rough estimate)
Density 1.58
refractive index 1.7040 (estimate)
solubility Acetonitrile (Very Slightly), Chloroform (Slightly), DMSO (Very Slightly)
form Solid:granular
Water Solubility 60 ppm (12 ºC), 90 ppm (50 ºC)
BRN 527184
CAS DataBase Reference 605-71-0(CAS DataBase Reference)
FDA UNII UI2S14IW4T
NIST Chemistry Reference Naphthalene, 1,5-dinitro-(605-71-0)
EPA Substance Registry System 1,5-Dinitronaphthalene (605-71-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H319-H335-H402-H317-H318-H341-H412
Precautionary statements  P201-P202-P264-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P308+P313-P405-P501-P273-P280-P305+P351+P338-P261-P501a
Hazard Codes  Xi,Xn
Risk Statements  41-43-52/53-68-36/37/38
Safety Statements  26-36/37/39-61-29
RIDADR  2811
WGK Germany  3
RTECS  QJ4551000
HazardClass  6.1(b)
PackingGroup  III
NFPA 704
1
2 0

1,5-Dinitronaphthalene Chemical Properties,Uses,Production

Chemical Properties

Yellow to yellow-green needles or fluffy powder

Uses

1,5-Dinitronaphthalene is an intermediate in the production of naphthazarin (5,8- dihydroxy-1,4-naphthoquinone) and 1,5- naphthalenediamine, which is mainly converted to naphthalene 1,5-diisocyanate. As a sensitizing agent for ammonium nitrate explosives the use of mixed isomers is adequate.

Definition

ChEBI: 1,5-dinitronaphthalene is a dinitronaphthalene carrying nitro groups at positions 1 and 5. It has a role as a genotoxin.

Production Methods

Naphthalene is added slowly to mixed acid (22/58/20) at 40 ℃, and the temperature is raised to 80 ℃ over 4 h to give a mixture of 1,5- and 1,8-dinitronaphthalenes. The isomers are separated by fractional crystallization (e.g., from ethylene dichloride) or, preferably, by solvent extraction. The 1,5-isomer can be extracted with toluene, leaving 99 % pure 1,8- dinitronaphthalene. After evaporation of the toluene, the residue is extracted with a strongly polar solvent (e.g., sulfolane) to leave 99 % pure 1,5-isomer.

General Description

Yellowish white needles or light yellow fluffy solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

1,5-Dinitronaphthalene is incompatible with strong oxidizers and strong bases. Mixtures with sulfur or sulfuric acid may explode if heated to 248° F .

Fire Hazard

Flash point data for 1,5-Dinitronaphthalene are not available; however, 1,5-Dinitronaphthalene is probably combustible.

Safety Profile

A suspected carcinogen. Mutation data reported. Mxtures with sulfur or sulfuric acid (used in commercial reactions) may explode if heated to 120℃. Initiation temperature depends on the quality of the dinitronaphthalene. When heated to decomposition it emits toxic fumes of NOx. See also NITRO COMPOUNDS of AROMATICHYDROCARBONS

1,5-dinitro-naphthalen Naphthalene,1,5-dinitro- 1,5-DINITRONAPHTHALENE LABOTEST-BB LT00436936 1,5-Dinitroaphthalene 1,5-Dinitronaphthalene98% 1,5-Dinitronaphthalene,tech.90% 1,5-DINITRO NAPHTALENE 1,5-Dinitronaphthalene, tech. 90% 1,5-Dinitronaphthalene, 97+% 1,5-Dinitronaphthalene, 98% 100GR 1.5-Dinitronaphthalene 10 1,5-Dinitronaphthalene >=97.0% (HPLC) 1,5-Dinitrophthalene 1,5-Dinitronaphthalene 602-38-0 605-71-0 C10H6NO22 Nitro Compounds Organic Building Blocks Nitrogen Compounds Building Blocks Building Blocks Chemical Synthesis Nitro Compounds Nitrogen Compounds Organic Building Blocks Nitro Compounds Nitrogen Compounds Organic Building Blocks Intermediates of Dyes and Pigments Naphthalene derivatives