TETRYL Property

Melting point:

130–132°C

Boiling point:

429.46°C (rough estimate)

Density 

1.57

vapor pressure 

<1 at 20 °C (NIOSH, 1997)

refractive index 

1.8000 (estimate)

Flash point:

2℃

storage temp. 

2-8°C

solubility 

Insoluble in water; soluble in ethanol, ether, benzene, acetic acid

form 

crystals

pka

12.66(at 25℃)

color 

Yellow

PH Range

11(colourless)-13(brown)

Water Solubility 

0.02 wt % at 20 °C (NIOSH, 1997)

Henry's Law Constant

<1.89 at 20 °C (approximate - calculated from water solubility and vapor pressure)

Exposure limits

(mg/m³): NIOSH REL: 1.5, IDLH 750; OSHA PEL: TWA 1.5; ACGIH TLV: TWA 1.5 (adopted).

Major Application

Explosives, paints, food storage

EPA Substance Registry System

Tetryl (479-45-8)

Safety

Hazard Codes 

E,T,F,Xn

Risk Statements 

2-23/24/25-33-36/37/38-11-36-20/21/22-3

Safety Statements 

35-45-27-16-36/37-26

RIDADR 

0208

WGK Germany 

2

HazardClass 

1.1D

Hazardous Substances Data

479-45-8(Hazardous Substances Data)

IDLA

750 mg/m3

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H225Highly Flammable liquid and vapour

H319Causes serious eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P337+P313IF eye irritation persists: Get medical advice/attention.

P403+P235Store in a well-ventilated place. Keep cool.

TETRYL Chemical Properties,Usage,Production

Description

This fully reduced quinoline type alkaloid has recently been obtained from the above-ground parts of Nitraria schoberi. The structure has been determined by ultraviolet, infrared, NMR and mass spectrometry. One hydroxyl and one methyl group are present and the alkaloid may be dehydrogenated in the presence of Pd-C to furnish 8-methylquinoline.

Chemical Properties

Yellow crystals. Insoluble inwater; soluble in alcohol, ether, benzene, glacial acetic acid.

Chemical Properties

Tetryl is a colorless to yellow, odorless crystalline solid. High explosive material.

Uses

As indicator, 0.1 g in 60 ml alcohol with water to make 100 ml. pH: 10.8 colorless, 13.0 reddish-brown. One to five drops of solution required for 10 ml liquid. Salt error said to be small. Also used in explosives.

Uses

Once widely used as a military explosive but no longer manufactured or used in the United States.

Uses

Tetryl is used as an initiator for many less sensitive explosives. It is used as the booster in artillery ammunition. A combination of Tetryl with trinitrotoluene and a small amount of graphite is known as Tetrytol, an explosive used as the bursting charge in artillery ammunition. It is also used as an indicator.
Tetryl is made by reacting 2,4-dinitrochlorobenzene with methylamine and nitrating the product with nitric acid and sulfuric acid.

Definition

ChEBI: A nitramine that is methylamine in which one of the hydrogens attached to the nitrogen is substituted by a nitro group while the other is substituted by a 2,4,6-trinitrophenyl group. A yellow crystalline powder, it is a high explosive, capable of being det nated by friction, shock, or a spark.

General Description

A yellow crystalline solid high explosive. Toxic by ingestion and skin absorption. A skin irritant. Will explode if heated above 370°F. Used as a detonating explosive. The primary hazard is the blast of an instantaneous explosion and not flying projectiles and fragments.

Reactivity Profile

During the measurement of the shock sensitivity of a mixture containing hydrazine, a drop of the hydrazine mixture fell on a TETRYL explosive. The TETRYL immediately burst into flames (ASESB 105).

Hazard

Dangerous fire and explosion risk. Skin irritant, absorbed by skin. Upper respiratory tract irritant.

Health Hazard

There is very little information on the human toxicity of this compound. A dose of 5000 mg/kg given subcutaneously was lethal to dogs (NIOSH 1986).

Fire Hazard

MAY EXPLODE AND THROW FRAGMENTS 1600 meters (1 MILE) OR MORE IF FIRE REACHES CARGO.

Safety Profile

Mutation data reported. An irritant, sensitizer, and allergen. The chief effect from exposure is dermatitis. Conjunctivitis is followed by iridocyclitis, and keratitis can occur. Sensitization produced by exposure may play a part in these symptoms. Gastrointestinal effects and anemia have also been reported. A powerful oxidant. A dangerous fire and explosion hazard. A high explosive sensitive to shock, friction, or heat. More sensitive to shock and friction than TNT. Explodes on contact with trioxygen difluoride. Ignites on contact with hydrazine. When heated to decomposition it emits toxic fumes of NOx. See also NITRATES and EXPLOSIVES, HIGH.

Potential Exposure

Tetryl is used in explosives; as an intermediary detonating agent; and as a booster charge for military devices; it is also used as a chemical indicator. No longer manufactured or used in the United States.

Carcinogenicity

A number of in vitro genotoxic assays in bacteria and fungi suggest that tetryl is a directacting genotoxin.

Environmental Fate

Chemical/Physical. Produces highly toxic nitrogen oxides on decomposition (Lewis, 1990).

Shipping

UN0208 Tetryl, Hazard Class: 1.1D; Labels:1.1D-Explosives (with a mass explosion hazard); D-Substances or articles which may mass detonate (with blast and/or fragment hazard) when exposed to fire.

Incompatibilities

Violent reaction with hydrazine; reducing agents, oxidizable materials. May explosively decompose from heat, shock, friction, or concussion. Explosive decomposition/detonation from heat takes approximately 1000 seconds @ 160℃; 0.1 seconds @ 500℃.

Waste Disposal

Solution in acetone and incineration in furnace equipped with afterburner and caustic soda solution scrubber.

References

Novgorodova, Maekh, Yunusov., Khirn. Prir. Soedin., 9, 196 (1973)