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DMDNB

Structure via PubChem · Public domain (PubChem)

EntityQ3267064· pop 13· linked from 7 articles

Also known as 2,3-dimethyl-2,3-dinitrobutane

DMDNB, or also DMNB, chemically 2,3-dimethyl-2,3-dinitrobutane, is a volatile organic compound used as a detection taggant for explosives, mostly in the United States where it is virtually the only such taggant in use. Dogs are very sensitive to it and can detect as little as 0.5 parts per billion in the air, as can specialised ion mobility spectrometers. Its presence allows more reliable explosive detection.

In the Vinony graph

Vinony's link graph records 7 inbound references to DMDNB, and connects out to United States, dog and explosive chemicals.

It is catalogued under topics including Chembox image size set, ECHA InfoCard ID from Wikidata and Explosive chemicals.

Vinony links it to 12 Wikipedia language editions.

Chemical data

Formula
C6H12N2O4
Molecular weight
176.17 g/mol
IUPAC name
2,3-dimethyl-2,3-dinitrobutane
SMILES
CC(C)(C(C)(C)[N+](=O)[O-])[N+](=O)[O-]
InChIKey
DWCLXOREGBLXTD-UHFFFAOYSA-N
XLogP
1
Polar surface area
91.6 Ų
H-bond donors
0
H-bond acceptors
4
Formal charge
0

via PubChem

Wikidata facts

Mass
176.079707
Show 3 more facts
canonical SMILES
CC(C)(C(C)(C)[N+](=O)[O-])[N+](=O)[O-]
chemical formula
C₆H₁₂N₂O₄
Commons category
2,3-Dimethyl-2,3-dinitrobutane
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

1 sections
Contents
  • References

DMDNB, or also DMNB, chemically 2,3-dimethyl-2,3-dinitrobutane, is a volatile organic compound used as a detection taggant for explosives, mostly in the United States where it is virtually the only such taggant in use. Dogs are very sensitive to it and can detect as little as 0.5 parts per billion in the air, as can specialised ion mobility spectrometers. Its presence allows more reliable explosive detection.

==References==

Excerpted from Wikipedia’s “DMDNB” article, available under the CC BY-SA 4.0 licence.

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