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ERR-001S

Supelco

RDX solution

1000 μg/mL in acetonitrile, ampule of 1.2 mL, certified reference material, Cerilliant®

Synonym(s):

Hexahydro-1,3,5-trinitro-1,3,5-triazine, Hexahydro-1,3,5-trinitro-1,3,5-triazine solution

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About This Item

Empirical Formula (Hill Notation):
C3H6N6O6
CAS Number:
121-82-4
Molecular Weight:
222.12
MDL number:
MFCD00458725
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material

Quality Level

300

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1.2 mL

manufacturer/tradename

Cerilliant®

concentration

1000 μg/mL in acetonitrile

application(s)

environmental

format

single component solution

storage temp.

−20°C

SMILES string

O=[N+]([O-])N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1

InChI

1S/C3H6N6O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H2

InChI key

XTFIVUDBNACUBN-UHFFFAOYSA-N

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Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup

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Hao-Ping Chen et al.
Applied and environmental microbiology, 78(21), 7798-7800 (2012-08-28)
Whole-genome sequencing, transcriptomic analyses, and metabolic reconstruction were used to investigate Gordonia sp. strain KTR9's ability to catabolize a range of compounds, including explosives and steroids. Aspects of this mycolic acid-containing actinobacterium's catabolic potential were experimentally verified and compared with
Muhammad Imran Khan et al.
Journal of microbiology and biotechnology, 22(10), 1311-1323 (2012-10-19)
In the present work, current knowledge on the potential fate, microbial degradation, and toxicity of hexahydro- 1,3,5-trinitro-1,3,5-triazine (RDX) was thoroughly reviewed, focusing on the toxicological assessment of a variety of potential RDX degradation pathways in bacteria and fungi. The present
Xiaoping Pan et al.
Environmental toxicology and chemistry, 32(6), 1295-1303 (2013-02-21)
Absorption, distribution, and biotransformation are 3 critical aspects affecting toxicant action in animals. In the present study, B6C3F1 mice (Mus musculus) were exposed for 28 d to contaminated feed that contained 1 of 5 different hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) concentrations: 0 mg/kg, 0.5 mg/kg
Ilana G Goldberg et al.
The journal of physical chemistry. A, 116(40), 9897-9899 (2012-09-15)
Recent studies of the crystallization of cyclotrimethylene-trinitramine (RDX) have shown that the presence of the α- and β-phases of the compound is sensitive to the substrate when using drop cast crystallization methods. The specific phase has potential consequences for measurements
Sridhar Jaligama et al.
Toxicology and applied pharmacology, 266(3), 443-451 (2012-12-12)
Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), a widely used munitions compound, and hexahydro-1-nitroso-3,5-dinitro-1,3,5-triazine (MNX), its N-nitroso product of anaerobic microbial nitroreduction, are contaminants of military sites. Previous studies have shown MNX to be the most acutely toxic among the nitroreduced degradation products of RDX
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