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Triallate

Triallate structure

Triallate 

structure
  • CAS No:

    2303-17-5

  • Formula:

    C10H16Cl3NOS

  • Chemical Name:

    Triallate

  • Synonyms:

    Carbamothioic acid,N,N-bis(1-methylethyl)-,S-(2,3,3-trichloro-2-propen-1-yl) ester;Carbamic acid,diisopropylthio-,S-(2,3,3-trichloroallyl) ester;Carbamothioic acid,bis(1-methylethyl)-,S-(2,3,3-trichloro-2-propenyl) ester;2-Propene-1-thiol,2,3,3-trichloro-,diisopropylcarbamate;CP 23426;Avadex BW;Far-Go;Triallate;S-2,3,3-Trichloroallyl N,N-diisopropylthiocarbamate;Dipthal;S-2,3,3-Trichloroallyl diisopropylthiocarbamate;2,3,3-Trichloroallyl N,N-diisopropylthiocarbamate;Triamyl;NSC 379698;Trillate;83903-69-9

  • Categories:

    Agrochemicals  >  Herbicides

Description

Oily liquid. Practically insoluble in water; soluble in alcohol, acetone, ether, and heptane. Combustible.

Triallate Basic Attributes

304.67

304.66

218-962-7

2930200013

Characteristics

45.6

3.98 (calculated)

Triallate, [solid] appears as colorless crystals or oily amber liquid. Toxic by inhalation, ingestion or skin absorption. Used as a pesticide.

1.273 g/cm3 @ Temp: 25 °C

29-30 °C

117 °C @ Press: 0.3 Torr

2 °C

1.532

H2O: 4.0 g/mL

APPROX 4°C

Vapour pressure, Pa at 25°C: 0.016

Relative vapour density (air = 1): 10.5

Oral-Rat LD50: 800 mg/kg; Oral-Mouse LD50: 930 mg/kg

Combustion produces toxic nitrogen oxides, chlorides and sulfur oxides

Combustible

Safety Information

I; II; III

6.1

UN 3077

3

22-43-48/22-50/53-36-20/21/22-11

24-37-60-61-36-26-16

EZ8575000

Xn;N,N,Xn,F

The warehouse is ventilated, low temperature and dry; stored and transported separately from food materials

Stable under normal storage conditions. Hydrolyzed by strong acids and alkalis.

P273-P280-P501

H302-H317-H373-H410

Toxicity

moderately toxic

Triallate Use and Manufacturing

Methods of Manufacturing

Dissolve 3g of sodium hydroxide in 20mL of water, mix with 5.5g (98%) of diisopropylamine at room temperature, cool the reaction solution to 0-5°C, and pass in carbon oxysulfide gas under stirring to absorb about 3g. A large amount of crystals precipitated, and the heat preservation reaction was continued. 18g (70%) 1, 1, 2, 3-tetrachloropropene was put into the reaction solution under stirring, and the reaction was continued at 0~65℃ for 6h, cooled to room temperature, and allowed to stand. Layer, the lower crude product is distilled under reduced pressure, and after the low-boiling substance is distilled off, the remaining amber viscous liquid is the product.

Uses

Herbicide.

Computed Properties

Molecular Weight:304.7
XLogP3:4.4
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:303.001818
Monoisotopic Mass:303.001818
Topological Polar Surface Area:45.6
Heavy Atom Count:16
Complexity:267
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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