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117501

Sigma-Aldrich

2,6-Dinitrobenzaldehyde

98%

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About This Item

Linear Formula:
(O2N)2C6H3CHO
CAS Number:
606-31-5
Molecular Weight:
196.12
Beilstein:
2113951
EC Number:
210-113-9
MDL number:
MFCD00007133
UNSPSC Code:
12352100
PubChem Substance ID:
24847333
NACRES:
NA.22

Assay

98%

form

solid

mp

120-122 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

SMILES string

[H]C(=O)c1c(cccc1[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C7H4N2O5/c10-4-5-6(8(11)12)2-1-3-7(5)9(13)14/h1-4H

InChI key

WHFZQNNDIJKLIO-UHFFFAOYSA-N

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General description

2,6-Dinitrobenzaldehyde is the major intermediate formed by the combined ozonation of 2,6-dinitrotoluene with hydrogen peroxide and UV radiation.

Application

2,6-Dinitrobenzaldehyde was used in the synthesis of free base tetrakis(2,6-dinitrophenyl) porphyrin.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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M Mori et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(7), 731-741 (1989-07-01)
1. Unchanged 2,6-dinitrotoluene (2,6-DNT), 2-amino-6-nitrotoluene, 2,6-dinitrobenzyl alcohol, 2-amino-6-nitrobenzyl alcohol, conjugated 2,6-dinitrobenzyl alcohol and conjugated 2-amino-6-nitrobenzyl alcohol were detected in urine of male Wistar rats dosed with 2,6-DNT. The major metabolite was conjugated 2,6-dinitrobenzyl alcohol, which accounted for about 1.5% of
Nitroaromatic hydrocarbon ozonation in water. 2. Combined ozonation with hydrogen peroxide or UV radiation.
Beltran FJ, et al
Industrial & Engineering Chemistry Research, 37(1), 32-40 (1998)
Synthesis and spectroscopic characterization of bis-pocket porphyrins: tetrakis (2', 6'-dinitrophenyl) porphyrin and catalytic activity of a manganese (III) chloride derivative in alkane oxidation.
Quintana CA, et al.
Inorganic Chemistry, 28(18), 3421-3425 (1989)
M Sayama et al.
Mutation research, 243(1), 47-52 (1990-01-01)
The mutagenicities and theoretical reactivity indices of 2,4-dinitrobenzaldehyde (2,4-DNBAl) and 2,6-dinitrobenzaldehyde (2,6-DNBAl) were investigated using Salmonella typhimurium strains TA98, TA98NR, TA98/1,8-DNP6, and TA100, TA100NR and TA100/1,8-DNP6, by means of the modified intermediate neglect of differential overlap/3 (MINDO)/3) method. The mutagenic

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