Cyclonite

HCID 8490CAS 121-82-4

Basic information

Standard SMILES
O=[N+]([O-])N1CN([N+](=O)[O-])CN([N+](=O)[O-])C1
InChIKey
XTFIVUDBNACUBN-UHFFFAOYSA-N
Molecular formula
C3H6N6O6
Average molar mass
222.12 g/mol
Monoisotopic mass
222.03488191

Overview

RDX stands for Royal Demolition eXplosive. It is also known as cyclonite or hexogen. The chemical name for RDX is 1,3,5-trinitro-1,3,5-triazine. It is a white powder and is very explosive. RDX is used as an explosive and is also used in combination with other ingredients in explosives. Its odor and taste are unknown. It is a synthetic product that does not occur naturally in the environment. It creates fumes when it is burned with other substances.

Names & identifiers

Preferred name
Cyclonite
IUPAC
1,3,5-trinitro-1,3,5-triazinane
English name
Hexahydro-1,3,5-trinitro-1,3,5-triazine
Molecular formula
C3H6N6O6
Molecular weight
222.12

Names & synonyms

CYCLONITEHexogenCyclotrimethylenetrinitramine121-82-4Hexahydro-1,3,5-trinitro-1,3,5-triazineGeksogenTrimethylenetrinitramineHexogen 5WHeksogenHexogeenHexogen (Explosive)1,3,5-Trinitro-1,3,5-triazacyclohexane
Show more names
RDX1,3,5-Trinitroperhydro-1,3,5-triazineT4pe4cx84ap-MSNDFNB24khp281
TrimethyleentrinitramineCyclotrimethylenenitramineCyklonitHexahydro-1,3,5-trinitro-s-triazine1,3,5-Triazine, hexahydro-1,3,5-trinitro-1,3,5-Trinitrohexahydro-s-triazineTrinitrotrimethylenetriaminePBX(AF) 108

Database identifiers

CAS
121-82-4
PubChem CID
8490
DTXSID
DTXSID9024142
ChEBI
CHEBI:24556
UNII
W91SSV5831
EC Number
204-500-1
Nikkaji
J2.368.951K、J2.412.206I、J5.346E

Properties

Computed structural properties

XLogP
1.6
Topological polar surface area
147 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
9
Rotatable bonds
0
Heavy atoms
15

Experimental & physicochemical properties

Chemical Classes · 2 items

Other Uses -> Explosives

Carcinogens

SpringerMaterials Properties15N nuclear magnetic resonance spectrum
PesticidesPesticide -> EPA IRIS
LogP · 3 items

log Kow = 0.87

0.87

0.87

Density · 6 items

1.82 (NIOSH, 2024) - Denser than water; will sink

1.82 g/cu cm at 20 °C

1.8 g/cm³

1.82

1.82 @25 °C

1.82

Color/Form · 3 items

White, crystalline powder

White crystalline solid

Orthorhombic crystals from acetone

Physicochemical properties

Melting point
205 · 205-206°
Boiling point
363.28 °C · 363.28°C (rough estimate)
Density
420 · d420 1.82
vapor pressure
0 Pa · 0Pa at 20℃
refractive index
1.67 · 1.6700 (estimate)
Flash point
2 ℃ · 2℃

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H201 (97.4%): (Deleted) Explosive; mass explosion hazard [Danger Explosives]

P210, P230, P240, P250, P260, P261, P262, P264, P270, P271, P280, P301+P316, P302+P352, P304+P340, P308+P316, P316, P319, P321, P330, P332+P317, P361+P364, P362+P364, P370+P380, P372, P373, P401, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 116 reports by companies from 18 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H201: (Deleted) Explosive; mass explosion hazard [Danger Explosives]

Hazard information

Regulatory Information · 6 items

Chemical: 1,3,5-Triazine, hexahydro-1,3,5-trinitro-

Hazard Traits - Carcinogenicity; Neurotoxicity

1,3,5-Triazine, hexahydro-1,3,5-trinitro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,3,5-Triazine, hexahydro-1,3,5-trinitro- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 23-09-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/13732

1,3,5-Triazine, hexahydro-1,3,5-trinitro-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - 1,3,5-Triazine, hexahydro-1,3,5-trinitro-: Human health tier I assessment
DOT Label · 2 items

Explosive 1.1D

Explosive 1.1D

Fire Hazards · 3 items

Excerpt from ERG Guide 112 [Explosives - Division 1.1, 1.2, 1.3 or 1.5]:

Excerpt from ERG Guide 112 [Explosives - Division 1.1, 1.2, 1.3 or 1.5]:

Gives off irritating or toxic fumes (or gases) in a fire. Risk of explosion. Explosive.

Fire PotentialDangerous due to fire ... hazard. /nitrates/
Health Hazards · 2 items

Excerpt from NIOSH Pocket Guide for Cyclonite:

Excerpt from ERG Guide 112 [Explosives - Division 1.1, 1.2, 1.3 or 1.5]:

Safety & protection

Fire Fighting · 3 items

Excerpt from ERG Guide 112 [Explosives - Division 1.1, 1.2, 1.3 or 1.5]:

Excerpt from ERG Guide 112 [Explosives - Division 1.1, 1.2, 1.3 or 1.5]:

Use water in large amounts, powder, carbon dioxide. Combat fire from a sheltered position. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 items

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Do NOT induce vomiting. Give a slurry of activated charcoal in water to drink. Refer immediately for medical attention.

First Aid · 3 items

Excerpt from NIOSH Pocket Guide for Cyclonite:

Excerpt from ERG Guide 112 [Explosives - Division 1.1, 1.2, 1.3 or 1.5]:

(General first aid procedures)

Safe StorageSubstance should be kept wet. Fireproof. Well closed. Separated from combustible substances and strong oxidizers. Store in an area without drain or sewer access.
Fire Fighting Procedures · 2 items

If material on fire or involved in fire: Dangerously explosive. Do not fight fires in a cargo of explosives. Evacuate area and let burn.

Evacuation: If the material is on fire or involved in fire consider evacuation of one (1) mile radius.

Storage ConditionsStore only in a permanent magazine. Protect container against physical damage. Store away from initiator explosives. Separate from oxidizing materials, combustibles & sources of heat.

Toxicology

Toxicological InformationCDC-ATSDR Toxicological Profile
Treatment · 1 item

Following oral exposure, symptomatic patients should be given adequate respiratory support during seizures. Monitor liver and renal function tests and urinalysis in patients with significant exposure. Following inhalation exposure, move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with inhaled beta2 agonist and oral or parenteral corticosteroids. Following eye exposure, irrigate exposed eyes with copious amounts of room temperature water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist, the patient should be seen in a health care facility. Following dermal exposure, remove contaminated clothing and wash exposed area thoroughly with soap and water. A physician may need to examine the area if irritation or pain persists. (T36)

Cancer SitesHepatic
Interactions · 2 items

In one study TNT and RDX were coadministered in the feed of rats for 13 weeks. This co-administration potentiated the decrease in body weight gain as compared to RDX alone. TNT antagonized the lethal effects and the hypotriglyceridemia induced by RDX. RDX antagonized the hypercholesterolemia, splenomegaly, testicular atrophy, hepatocytomegaly, degeneration of the seminiferous tubules, and pigmentation of renal cortices induced by TNT. Investigated the effects of a mixture of 10% RDX and 0.32% TNT in dogs, rats, and mice. All three species showed depression of body weight gain, depressed food intake, and alterations in the spleen, liver, and testes at the highest dose levels. However, RDX was not tested alone.

Explosive compounds such as TNT and RDX are recalcitrant contaminants often found co-existing in the environment. In order to understand the joint effects of TNT and RDX on earthworms, an important ecological and bioindicator species at the molecular level, we sampled worms (Eisenia fetida) exposed singly or jointly to TNT (50 mg/kg soil) and RDX (30 mg/kg soil) for 28 days and profiled gene expression in an interwoven loop designed microarray experiment using a 4k-cDNA array. Lethality, growth and reproductive endpoints were measured. Sublethal doses of TNT and RDX had no significant effects on the survival and growth of earthworms, but significantly reduced cocoon and juvenile counts. The mixture exhibited more pronounced reproductive toxicity than each single compound, suggesting an additive interaction between the two compounds. In comparison with the controls, we identified 321 differentially expressed transcripts in TNT treated worms, 32 in RDX treated worms, and only 6 in mixture treated worms. Of the 329 unique differentially expressed transcripts, 294 were affected only by TNT, 24 were common to both TNT and RDX treatments, and 3 were common to all treatments. The reduced effects on gene expression in the mixture exposure suggest that RDX might interact in an antagonistic manner with TNT at the gene expression level. The disagreement between gene expression and reproduction results may be attributed to sampling time, absence of known reproduction-related genes, and lack of functional information for many differentially expressed transcripts. A gene potentially related to reproduction (echinonectin) was significantly depressed in TNT or RDX exposed worms and may be linked to reduced fecundity. Sublethal doses of TNT and RDX affected many biological pathways from innate immune response to oogenesis, leading to reduced reproduction without affecting survival and growth. A complex interaction between mixtures of RDX and TNT was observed at the gene expression level that requires further study of the dynamics of gene expression and reproductive activities in E. fetida. These efforts will be essential to gain an understanding of the additive reproductive toxicity between RDX and TNT.

Target Organs · 3 items

Hematological (Blood Forming), Hepatic (Liver), Neurological (Nervous System)

Nervous

Eyes, skin, central nervous system

Health EffectsRDX can cause seizures. Inhalation exposure to RDX can lead to gastrointestinal, hematological, hepatic, and renal effects. (L259)

Regulatory information

TSCA Requirements · 2 items

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, exposure, and use to EPA as cited in the preamble in 51 FR 41329. Effective date 9/29/06; Reporting date: 11/28/06.

[40 CFR 716.120] Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. 1,3,5-Triazine, hexahydro-1,3,5-trinitro- is included on this list. Effective date: 9/29/06; Sunset date: 11/28/09.

DHS Chemicals of Interest (COI) · 6 items

Hexolite

A Commercial Grade

5000

A Commercial Grade

400

Explosive chemical that can be released at a facility.

State Drinking Water Guidelines · 2 items

(FL) FLORIDA 10 ug/L

(ME) MAINE 3 ug/L

Federal Drinking Water GuidelinesEPA 2 ug/L

Safety data

OEB
B
OEL
TWA: 1.5 mg/m3, STEL: 3 mg/m3 [skin]
wgk
2
tsca
TSCA listed
ridadr
UN 0483 1.1D (CYCLOTRIMETHYLENE- TRINITRAMINE (CYCLONITE; HEXOGEN; RDX), DESENSITIZED)
hs_code
29339900

Chemistry & industry

Pharmacology

Mechanism of Action · 3 items

Munitions constituents (MCs) including hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), 2,4,6-trinitrotoluene (TNT), and TNT derivatives are recognized to elicit aberrant neuromuscular responses in many species. The onset of seizures resulting in death was observed in the avian model Northern bobwhite after oral dosing with RDX beginning at 8 mg/kg/day in subacute (14 days) exposures, whereas affective doses of the TNT derivative, 2,6-dinitrotoluene (2,6-DNT), caused gastrointestinal impacts, lethargy, and emaciation in subacute and subchronic (60 days) exposures. To assess and contrast the potential neurotoxicogenomic effects of these MCs, a Northern bobwhite microarray was developed consisting of 4119 complementary DNA (cDNA) features enriched for differentially-expressed brain transcripts from exposures to RDX and 2,6-DNT. RDX affected hundreds of genes in brain tissue, whereas 2,6-DNT affected few (<or= 17), indicating that 2,6-DNT exposure had relatively little impact on the brain in comparison to RDX. Birds exhibiting RDX-induced seizures accumulated over 20x more RDX in brain tissues in comparison to non-seizing birds even within a common dose. In parallel, expression patterns were unrelated among seizing and non-seizing birds exposed to equivalent RDX doses. In birds experiencing seizures, genes related to neuronal electrophysiology and signal transduction were significantly affected. Comparative toxicology revealed strong similarity in acute exposure effects between RDX and the organochlorine insecticide dichlorodiphenyltrichloroethane (DDT) regarding both molecular mechanisms and putative mode of action. In a manner similar to DDT, RDX /may/ elicits seizures by inhibition of neuronal cell repolarization postaction potential leading to heightened neuronal excitability and seizures facilitated by multiple molecular mechanisms.

Arabidopsis thaliana root transcriptome responses to the munition, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), were assessed using serial analysis of gene expression (SAGE). Sequencing of SAGE libraries from control and RDX-exposed root tissues revealed induction of genes known to respond to a variety of general stresses. Among the highly induced genes were several encoding molecular chaperones and transcription factors as well as vacuolar proteins and peroxidases. Strongly repressed transcripts included ones encoding ribosomal proteins, a cyclophilin, a katanin, and a peroxidase. Comparison of the transcriptional profile for the RDX response to a profile previously described for Arabidopsis roots exposed to trinitrotoluene (TNT) revealed significant differences in the inferred gene expression patterns. This suggests that Arabidopsis employs drastically different mechanisms for coping with these two compounds. With respect to the goal of engineering plants to better tolerate and degrade explosives at contaminated sites, these results suggest that enhancement of different genes and metabolic pathways may be required to deal effectively with each type of explosive. This has ramifications for phytoremediation efforts since many contaminated sites harbor both compounds.

Hexahydro-1,3,5-trinitro-1,3,5-triazine is a synthetic, high-impact, relatively stable compound commonly known as Rapid Detonation Explosive (RDX) ...Though several studies have correlated measurements of RDX in the brains and plasma of dosed animals with frank seizures, little work has been carried out on the effects of RDX at the molecular level. In this study, we examined the impact of a single orally administered RDX dose on the brain, using a combination of analytical chemistry and gene chip microarrays. At nominal doses of 3 and 18 mg/kg in male adult rats, a time course of RDX tissue levels showed peak brain concentrations at 3.5 hours, returning to baseline at 24 and 48 hours, respectively. RNA from dosed and control animals was hybridized to Affymetrix Rat 230 2.0 arrays. Analysis was performed in JMP Genomics with the differentially expressed gene cut-off at p>0.001. /The study/ found sets of genes that were early and late responders to RDX treatment. In addition, pathway analysis indicated effects on the nervous system, cell-to-cell signalling, and cell development, among other...

Biological Half-Life · 1 item

The extensively used military explosive hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) has been widely released to the environment during production, usage, and disposal operations. Toxic effects of RDX have been reported in terrestrial and aquatic receptors, but investigations regarding the bioaccumulation potential of RDX in aquatic systems are scarce. The objective of the present study was to describe the toxicokinetics of RDX during aqueous exposure for the channel catfish (Ictalurus punctatus) and aquatic oligochaetes (Lumbriculus variegatus) and to compare the amount of RDX accumulation in juvenile catfish following aqueous exposure only, dietary exposure only, and a combination of dietary and aqueous exposure. The toxicokinetics measurements included bioconcentration factors (BCFs), uptake rates, elimination rates, and biological half-lives. First-order, single-compartment models described the toxicokinetics for both species. Uptake of RDX into oligochaetes was relatively rapid (uptake clearance constant [k(u)] of 5.17 mL/g/hr) compared to that in catfish (k(u) = 1.28 mL/g/hr). However, elimination also was more rapid in oligochaetes, with biological half-lives of 0.28 and 1.09 hr for oligochaetes and catfish, respectively. Thus, both species had very similar estimated BCFs of 2.1 mL/g for oligochaetes and 2.0 mL/g for catfish. Accumulation of RDX in fish that were fed oligochaetes exposed to an exceedingly high water concentration of RDX was minimal. The present investigation indicates that RDX uptake via the aqueous route is the expected dominant uptake pathway, with dietary uptake contributing minimally to the overall body burden in fish inhabiting RDX-contaminated sites. Because of the exceedingly low bioaccumulative potential and low reported toxicity of RDX, the presence of this explosive in aquatic systems is unlikely to pose unacceptable risks to invertebrates and fish.

Metabolism/Metabolites · 6 items

Poplar plants (Populus deltoides x nigra, DN34) growing under hydroponic conditions were exposed to 50 mg /per/ L of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) for 24 hr. The expression of genes potentially involved in the metabolism of toxic explosives was analyzed by reverse-transcriptase (RT) real-time PCR. Genes under study were selected by reference to corresponding genes that were previously shown to be upregulated in the model plant Arabidopsis thaliana by exposure to 2,4,6-trinitrotoluene (TNT)... The target genes investigated include several genes encoding for enzymes known to be involved in the detoxification of xenobiotic pollutants, such as glutathione S-transferases (GSTs), cytochrome P-450s (CYPs), NADPH-dependent reductases, and peroxidases. Starting from A. thaliana TNT-inducible genes, corresponding Populus sequences were retrieved from the JGI Poplar Genome Project database and were used to design gene-specific primers. 18S ribosomal DNA (rDNA) was used as an internal standard and recorded gene expression levels were normalized by reference to nonexposed plants. In three separate experiments, five genes were found to be significantly amplified in leaf tissues by exposure to RDX, including GST (9.7 fold), CYP (1.6 fold), reductases (1.6-1.7 fold), and peroxidase (1.7 fold). In root tissues, only a single GST gene was found to be significantly amplified by exposure to RDX (2.0 fold). These results show, for the first time, that the exposure of poplar plants to RDX results in the induction of several genes that are potentially involved in explosive detoxification.

The study ... examined the metabolism of (14)C-labeled hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) resulting from a single oral gavage of 5 mL/kg to male and female Yucatan miniature pigs (43 mg/kg, 56 microCi/kg in 0.5% carboxymethylcellulose in water). Blood, urine, and feces were collected at selected times of 1, 6, 12, and 24 hr post dose. At 24 hr post dose, liver samples were collected. Blood, plasma, liver, and excreta were analyzed for total RDX-derived radioactivity and metabolites were identified. ... Analysis of urine by liquid chromatography-mass spectrometry (LC/MS) identified quantifiable levels of two ring-cleavage metabolites, 4-nitro-2,4-diazabutanal and 4-nitro-2,4-diaza-butanamide, as well as parent RDX. ... Analysis by a more sensitive method (LC/MS/MS) also showed trace amounts of the RDX metabolites 1-nitroso-3,5-dinitro-1,3,5-triazacyclohexane (MNX) (in both male and female urine) and 1-nitro-3,5-dinitroso-1,3,5-triazacyclohexane (DNX) (in male urine). Analysis of plasma by LC/MS/MS also revealed quantifiable levels of RDX and trace levels of MNX, DNX, and 1,3,5-trinitroso-1,3,5-triazacyclohexane (TNX). None of the liver extracts showed quantifiable levels of RDX or any identifiable metabolites. Most of the radioactivity was in the form of water-soluble high-molecular-weight compounds. RDX when given orally to pigs was rapidly metabolized by loss of two nitro groups followed by ring cleavage.

Sprague-Dawley rats of both sexes (200-250 g) were either dosed with unlabeled or (14)C-RDX by gavage at 20 mg/kg/day for up to 90 days or allowed free access to unlabeled RDX or (14)C-RDX-saturated drinking water (50-70 ug/mL) for up to 90 days. The majority of the label was excreted as exhaled (14)C-carbon dioxide and as unidentified metabolites in the urine.

...A cytochrome P450 2B4 from rabbit liver catalyzed a biotransformation of RDX to 4-nitro-2,4-diazabutanal. Both the cytochrome P450 2B4 and intact cells of Rhodococcus sp. strain DN22 catalyzed the release of two nitrite ions from each reacted RDX molecule. A comparative study of cytochrome P450 2B4 and Rhodococcus sp. strain DN22 revealed substantial similarities in the product distribution and inhibition by cytochrome P450 inhibitors.

For more Metabolism/Metabolites (Complete) data for CYCLONITE (9 total), please visit the HSDB record page.

There are no studies available regarding RDX metabolites in humans following inhalation, oral, or dermal exposure. Some studies reported that 4-nitro-2,4-diazabutanal, and nitrite ions are produced through biotransformation of RDX by cytochrome P450. The limited toxicological data show that RDX is absorbed through the gastrointestinal system, lungs, and skin, and is distributed to the cerebrospinal fluid, plasma, urine, and feces. RDX will leaves the body in the breath and urine within a few days. (L259,A162)

MeSH Pharmacological Classification · 2 items

Substances used to destroy or inhibit the action of rats, mice, or other rodents.

Substances that are energetically unstable and can produce a sudden expansion of the material, called an explosion, which is accompanied by heat, pressure and noise. Other things which have been described as explosive that are not included here are explosive action of laser heating, human performance, sudden epidemiological outbreaks, or fast cell growth.

Absorption, Distribution and Excretion · 5 items

The study ... examined the metabolism of (14)C-labeled hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) resulting from a single oral gavage of 5 mL/kg to male and female Yucatan miniature pigs (43 mg/kg, 56 uCi/kg in 0.5% carboxymethylcellulose in water). Blood, urine, and feces were collected at selected times of 1, 6, 12, and 24 hr post dose. At 24 hr post dose, liver samples were collected. Blood, plasma, liver, and excreta were analyzed for total RDX-derived radioactivity and metabolites were identified. Urine was the major route of elimination of (14)C-RDX-derived radioactivity in both males and females. Relatively low levels of radioactivity were found in gastrointestinal contents and in feces, suggesting nearly complete absorption of (14)C-RDX following an oral dose. ...

... The toxicokinetics of (14)C-RDX-derived radioactivity was examined following administration of a single oral dose formulated as an aqueous suspension in 0.1% carboxymethylcellulose at a target dose level of 43 mg/kg ... to male and female Yucatan mini pigs. Blood was collected at 1, 6, 12 and 24 hr post dose from each animal. Urine and feces were collected through 24 hr post dose. ... Urine was the major route for elimination of (14)C-RDX-derived radioactivity, with 17.3 and 17.6% of the radioactive dose, respectively, in males and females. RDX was well absorbed. Feces accounted for less than 1% of administered dose and gastrointestinal contents for about 5.6% of the dose. The distribution of (14)C-RDX derived radioactivity was extensive, with radioactivity observed in all collected tissues. The highest concentrations of radioactivity were observed in liver and kidney. The calculated percent of radioactive dose was high in liver (3.5 to 5.8%) and muscle (2.5 to 4.7%).

It is slowly absorbed from the stomach and apparently from the lungs, but there is no evidence of skin absorption.

Sprague-Dawley rats of both sexes (200-250 g) were either dosed with unlabeled or (14)C-RDX by gavage at 20 mg/kg/day for up to 90 days or allowed free access to unlabeled RDX or (14)C-RDX-saturated drinking water (50-70 ug/mL) for up to 90 days. RDX did not accumulate in any tissue examined nor were there any tendencies for plasma RDX to increase continuously with repeated dosing in rats. In the 90-day drinking water study the daily recovery of the (14)C label, estimated at the end of 1, 4, 8, and 13 wk, varied between 54 and 89%. The majority of the label was excreted as exhaled (14)-carbon dioxide and as unidentified metabolites in the urine.

For more Absorption, Distribution and Excretion (Complete) data for CYCLONITE (12 total), please visit the HSDB record page.

Uses & manufacturing

Uses · 5 items

Used as an explosive and rodenticide; [ACGIH]

Transportation forbidden for Cyclonite; Transportation forbidden by passenger aircraft/rail and cargo aircraft for Cyclonite (desensitized or wetted with >15% water; [HMT]

High explosive

It has been widely used as a base charge for detonators and as an ingredient of bursting-charge and plastic explosives by the military.

RDX is used as an explosive and is also used in combination with other ingredients in explosives. Exposure may occur by breathing dust containing RDX, contact with the skin, or drinking contaminated water. (L259)

Impurities · 2 items

Impure military grades ... /contain/ about 10% HMX /hexamethylenetetramine/ ...

Many other by-products are formed during the Bachmann process but may not always be present: 1,5-endo-methylene-3,7-dinitro-1,3,5,7-tetrazacyclooctane; 1,7-diacetoxy-2,4,6-trinitro-2,4,6-triazaheptane; 1,5-endo-ethylene-3,7-dinitro-1,3,5,7-tetrazacyclooctane; 1,5-endo-ethylidine-3,7-dinitro-1,3,5,7-tetrazacyclooctane; 1-nitro-3,5--dicyclohexyl-1,3,5-triazacyclohexane; N,N'-dimethylol-N,N'-dicyclohexyldiaminoethane; 3,7-dinitro-3,7-diaza-1,5-dioxacyclooctane; dinitroxydimethylnitramide; diacetoxydimethylnitramide; 1,3,5-trinitroso-1,3,5-triazacyclohexane.

U.S. Production · 6 items

2023: 7,000,000 - <8,500,000 lb

The production of cyclonite (RDX) was listed as 102X10+6 lb in l972.

Production of RDX peaked in the 1960s when it was ranked third in explosive production by volume in the United States. The average volume of RDX produced from 1969 to 1971 was 15 million pounds per month. However, production of RDX decreased to a yearly total of 16 million pounds for 1984.

1,3,5-Triazine, hexahydro-1,3,5-trinitro- is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#3839]

Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: 1,3,5-Triazine, hexahydro-1,3,5-trinitro-. Aggregated National Production Volume: 1 to < 10 million pounds.

Consumption PatternsAPPROX 100% IN EXPLOSIVES FOR MILITARY USE (1975)
Consumer UsesEnergy Releasers (explosives, motive propellant)
Industry UsesEnergy Releasers (explosives, motive propellant)
Applications · 4 items

DescriptionHexahydro-1,3,5-trinitro-s-triazine is a whitecrystalline compound; Boiling point=.260℃; Freezing/Melting point=203-204℃; Exothermicdecomposition=100℃; Hazard Identification (based onNFPA-704 M Rating System): Health 2, Flammability(explosive), Reactivity (see incompatibilities). Insoluble inwater

UsesCyclonite is a high explosive and principal constituent of plastic bombs. It is preparedby treating hexamethylenetetramine with nitric acid,ammoniumnitrate,andaceticanhydride: It is also used as a rat poison.

UsesHigh explosive; rodenticide.RDX is a convulsant.

General DescriptionCyclotrimethylene trinitramine is an explosive. The explosion can be initiated by a sudden shock, high temperature or a combination of the two. The primary hazard is from blast effect and not from flying projectiles and fragments. Under prolonged exposure to heat or fire they can explode.

Upstream & downstream products

Upstream raw materials

Additional notes · 2 items

DefinitionCyclonite: A highly explosive nitrocompound, (CH2N.NO2)3. It has acyclic structure with a six-memberedring of alternating CH2 groups andnitrogen atoms, with each nitrogenbeing attached to a NO2 group. It ismade by nitrating hexamine,C6H12N4, which is obtained from ammoniaand methanal. Cyclonite is avery powerful explosive used mainlyfor military purposes. It is also calledRDX. The abbreviation is for ‘ResearchDepartment composition X’,used at the Chemical Research andDevelopment Department, Woolwich.

DefinitionChEBI: An N-nitro compound that is 1,3,5-triazinane in which all three of the hydrogens attached to the nitrogens have been replaced by nitro groups. It is widely used in both industrial and military explosives.

Related reactions

4 records

Linked notes

Loading…