ANILAZINE Chemical Properties

Melting point:

159-160℃

Boiling point:

425.99°C (rough estimate)

Density 

1.611

refractive index 

1.6000 (estimate)

storage temp. 

0-6°C

pka

0.43±0.10(Predicted)

Water Solubility 

10mg/L(temperature not stated)

Merck 

13,659

BRN 

223133

Exposure limits

The German Research Society’s recommended Maximum Allowable Concentration is 0.2 mg/m3.

Stability:

Stable. Incompatible with oils and alkalies. May corrode some types of metal and alloy.

CAS DataBase Reference

101-05-3(CAS DataBase Reference)

EPA Substance Registry System

Anilazine (101-05-3)

Safety Information

Hazard Codes 

Xi,N

Risk Statements 

36/38-50/53

Safety Statements 

22-60-61

RIDADR 

UN3077 9/PG 3

WGK Germany 

3

RTECS 

XY7175000

Hazardous Substances Data

101-05-3(Hazardous Substances Data)

Toxicity

LD50 orally in rats: >5000 mg/kg, Mobay Technical Information Sheet, Jan. 1979

ANILAZINE Usage And Synthesis

Chemical Properties

white to light brown crystals or powder

Uses

Pesticide used to control fungus diseases in lawns and turf.

Uses

Nonsystemic, foliar fungicide used in potatoes, tomatoes, wheat, barley and ornamentals.

Uses

Fungicide.

Definition

ChEBI: A member of the class of triazenes that is dichlorotriazene in which the hydrogen is replaced by an o-chloroanilino group. A fungicide formerly used to control leaf spots and downy mildew, it is no longer approved for use within the European U ion.

General Description

White to tan crystals or white powder. Moderately soluble in organic solvents. Insoluble in water. Melting point 159°C.

Air & Water Reactions

Insoluble in water. Stable in neutral and slightly acidic aqueous media but hydrolyzes on heating with alkali.

Reactivity Profile

ANILAZINE is incompatible with oils and alkalis. ANILAZINE is slightly corrosive to metals.

Fire Hazard

Flash point data for ANILAZINE are not available; however, ANILAZINE is probably combustible.

Environmental Fate

Soil. Anilazine is readily degraded by soil bacteria (Harris et al., 1968). The reported half-life of anilazine in soil is approximately 12 hours (Hartley and Kidd, 1987)
Plant. In plants, one or both of the chlorine atoms on the triazine ring may be replaced by thio or amino groups (Hartley and Kidd, 1987)
Chemical/Physical. Anilazine is subject to hydrolysis (Windholz et al., 1983) releasing chlorine gas (Hartley and Kidd, 1987)

ANILAZINE(101-05-3)Related Product Information

• 2,4-BIS(TRICHLOROMETHYL)-6-[2-(FURAN-2-YL)VINYL]-1,3,5-TRIAZINE
• 2,4,6-TRIS(DIMETHYLAMINO)-1,3,5-TRIAZINE
• 2，4，6-Tris(allyloxy)triazine,2,4,6-TRIS(ALLYLOXY)-1,3,5-TRIAZINE,2,4,6-TRIS(ALLYLOXY)S-TRIAZINE
• 1,1'-[(6-phenyl-1,3,5-triazine-2,4-diyl)diimino]bisanthraquinone
• 2,4,6-TRIS(NONADECAFLUORONONYL)-S-TRIAZINE,2,4,6-TRIS(PERFLUORONONYL)-1,3,5-TRIAZINE,2,4,6-TRIS(PERFLUORONONYL)-S-TRIAZINE
• 2,4-BIS ISOPROPYLAMINO-6-METHYLTHIO-S-TRIAZINE
• 2,4-Dichloro-1,3,5-triazine
• 2-Amino-4,6-dichlorotriazine
• 2 4-BIS(ETHYLAMINO)-6-CHLORO-SYM-TRIAZINE,2,4-BIS(ETHYLAMINO)-6-CHLORO-1,3,5-TRIAZINE,2,4-bis(ethylamino)-6-chloro-s-triazine
• 2,4,6-TRIS(TRIFLUOROMETHYL)-1,3,5-TRIAZINE
• 2,4,6-TRIS(HEPTAFLUOROPROPYL)-1,3,5-TRIAZINE,2,4,6-TRIS(HEPTAFLUOROPROPYL)-S-TRIAZINE,2,4,6-TRIS(PERFLUOROPROPYL)-S-TRIAZINE
• 2,4-bis(allylamino)-6-[4-[bis(p-fluorophenyl)methyl]-1-piperazinyl]-s-triazine dimethanesulfonate
• 2,4,6-TRIS[BIS(METHOXYMETHYL)AMINO]-1,3,5-TRIAZINE
• 2-(4-Methoxystyryl)-4,6-bis(trichloromethyl)-1,3,5-triazine
• 2,4,6-TRIS[BIS(METHOXYMETHYL)AMINO]-1,3,5-TRIAZINE
• Simetryne
• 2,4,6-TRIS(CHLOROAMINO)-1,3,5-TRIAZINE,2,4,6-tris(chloroamino)-s-triazine
• 2，4-Bis(ethylamino)-6-methoxy-s-triazine