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Merck
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Key Documents

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ERR-001S

Supelco

RDX solution

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

Sinónimos:

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

Fórmula empírica (notación de Hill):
C3H6N6O6
Número de CAS:
121-82-4
Peso molecular:
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

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
Anat Bernstein et al.
Environmental science & technology, 47(1), 479-484 (2012-12-12)
The explosive Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is known to be degraded aerobically by various isolates of the Rhodococcus species, with denitration being the key step, mediated by Cytochrome P450. Our study aimed at gaining insight into the RDX degradation mechanism by Rhodococcus
Karl K Irikura
The journal of physical chemistry. A, 117(10), 2233-2241 (2013-02-05)
The explosive nitramine RDX (1,3,5-trinitrohexahydro-s-triazine) is thought to decompose largely by homolytic N-N bond cleavage, among other possible initiation reactions. Density-functional theory (DFT) calculations indicate that the resulting secondary aminyl (R2N·) radical can abstract an oxygen atom from NO2 or
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
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