2,4,6-Trinitro-m-cresol

2,4,6-Trinitro-m-cresol Basic information
Product Name:2,4,6-Trinitro-m-cresol
Synonyms:2,4,6-Trinitro-m-cresol;Cresylite;TNcr;Phenol, 3-methyl-2,4,6-trinitro-
CAS:602-99-3
MF:C7H5N3O7
MW:243.13
EINECS:210-027-1
Product Categories:
Mol File:602-99-3.mol
2,4,6-Trinitro-m-cresol Structure
2,4,6-Trinitro-m-cresol Chemical Properties
Melting point 109.5°C
Boiling point 385.99°C (rough estimate)
density 1.7550 (rough estimate)
refractive index 1.5500 (estimate)
pka1.16±0.10(Predicted)
Water Solubility 2.431g/L(25 ºC)
EPA Substance Registry SystemPhenol, 3-methyl-2,4,6-trinitro- (602-99-3)
Safety Information
Hazard Codes E,Xn
Risk Statements 2-4-20/21/22
Safety Statements 35
RIDADR 0216
HazardClass 1.1D
PackingGroup II
Hazardous Substances Data602-99-3(Hazardous Substances Data)
MSDS Information
2,4,6-Trinitro-m-cresol Usage And Synthesis
UsesBursting charges and other high explosive uses.
General DescriptionA detonating explosive in the form of yellow needles. Readily soluble in alcohol, ether, and acetone. Primary hazard is blast of an instantaneous explosion, not flying projectiles or fragments. Under prolonged exposure to fire or heat the containers may explode violently.
Air & Water ReactionsSlightly soluble in water.
Reactivity Profile2,4,6-Trinitro-m-cresol is a nitroaryl derivative. 2,4,6-Trinitro-m-cresol is sensitive to heat. Nitroaryls range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.
Health HazardFire may produce irritating, corrosive and/or toxic gases.
Fire HazardMAY EXPLODE AND THROW FRAGMENTS 1600 meters (1 MILE) OR MORE IF FIRE REACHES CARGO.
Purification MethodsCrystallise the cresol successively from H2O, aqueous EtOH and *benzene/cyclohexane, then dry at 80o for 2hours. [Davis & Paabo J Res Nat Bur Stand 64A 533 1960, Beilstein 6 H 387, 6 I 194, 6 II 363, 6 III 1331, 6 IV 2079.]
2,4,6-Trinitro-m-cresol Preparation Products And Raw materials
Tag:2,4,6-Trinitro-m-cresol(602-99-3) Related Product Information
m-Cresol Cresol