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Key Documents

79874

Sigma-Aldrich

2-Chloro-1,3,5-trinitrobenzene

≥98.0% (HPLC)

Synonym(s):

2,4,6-Trinitrochlorobenzene

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About This Item

Empirical Formula (Hill Notation):
C6H2ClN3O6
CAS Number:
Molecular Weight:
247.55
Beilstein:
1588666
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98.0% (HPLC)

form

lumps

SMILES string

[O-][N+](=O)c1cc(c(Cl)c(c1)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C6H2ClN3O6/c7-6-4(9(13)14)1-3(8(11)12)2-5(6)10(15)16/h1-2H

InChI key

HJRJRUMKQCMYDL-UHFFFAOYSA-N

Other Notes

moistened with ~15% water

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Sol. 1

Supplementary Hazards

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Hagiyama et al.
The British journal of dermatology, 168(4), 771-778 (2012-10-31)
Neuroimmunological disorders are involved in the pathogenesis of atopic dermatitis (AD), partly through enhanced sensory nerve-skin mast cell interaction. Cell adhesion molecule 1 (CADM1) is a mast-cell adhesion molecule that mediates the adhesion to, and communication with, sympathetic nerves. To
Eujin Cho et al.
Journal of ethnopharmacology, 145(1), 294-302 (2012-11-15)
Korean red ginseng (KRG) has been shown to possess various biological activities including anti-inflammatory properties. We aimed to investigate the effects and mechanism of KRG on the prevention of atopic dermatitis (AD) using a mouse model. The effect of KRG
Atsuto Ogata et al.
International immunopharmacology, 11(10), 1628-1632 (2011-06-07)
A chymase inhibitor SUN13834 has been shown to improve skin condition in animal models for atopic dermatitis. In the present study, effective dosages of SUN13834 for atopic dermatitis patients were predicted by pharmacokinetic/pharmacodynamic (PK/PD) analyses of SUN13834 in NC/Nga mice
Andreas Natsch et al.
Chemical research in toxicology, 24(11), 2018-2027 (2011-10-26)
The skin sensitization potency of chemicals is partly related to their reactivity to proteins. This can be quantified as the rate constant of the reaction with a model peptide, and a kinetic profiling approach to determine rate constants was previously
Eriko Suwa et al.
European journal of pharmacology, 667(1-3), 383-388 (2011-06-15)
Effects of the histamine H(4) receptor antagonist 1-[(5-chloro-1H-indol-2-yl)carbonyl]-4-methylpiperazine (JNJ7777120) were examined for 99 days in a long-term experimental model of pruritic dermatitis induced by repeated challenge with 2,4,6-trinitrochlorobenzene (TNCB) in HR-1 mice. Repeated application of TNCB to the back skin

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