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Merck
CN

N13628

Triallat

analytical standard

Synonym(s):

S-(2,3,3-Trichloroallyl) N,N-diisopropylthiocarbamate

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About This Item

Empirical Formula (Hill Notation):
C10H16Cl3NOS
CAS Number:
Molecular Weight:
304.66
EC Number:
218-962-7
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1875853
MDL number:
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InChI key

MWBPRDONLNQCFV-UHFFFAOYSA-N

InChI

1S/C10H16Cl3NOS/c1-6(2)14(7(3)4)10(15)16-5-8(11)9(12)13/h6-7H,5H2,1-4H3

SMILES string

CC(C)N(C(C)C)C(=O)SC\C(Cl)=C(/Cl)Cl

grade

analytical standard

packaging

ampule of 1 g

manufacturer/tradename

Chem Service, Inc. PS-506

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

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C Sanchez-Brunete et al.
Journal of chromatography, 562(1-2), 525-530 (1991-01-02)
Triallate residues in barley seedlings and soil samples were determined by gas chromatography with ion-trap detection. Soil was extracted with methanol on a mechanical shaker, and plants were extracted with acetonitrile in a Sorvall homogenizer. After evaporation of the organic
Microsomal hydroxylation of triallate: identification of a 2-chloroacrylate glutathione conjugate using heteronuclear multiple quantum coherence NMR spectroscopy.
A G Hackett et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(6), 1163-1165 (1991-11-01)
B R Blakley et al.
Veterinary and human toxicology, 40(1), 5-10 (1998-02-19)
The commercial formulations of 3 commonly used herbicides (the amine salt of 2,4-dichlorophenoxyacetic acid, trifluralin and triallate) were evaluated for effects on immune function in male Fisher 344 rats. The herbicides were prepared in an olive oil vehicle and administered
Angela Volpe et al.
Chemosphere, 57(7), 579-586 (2004-10-19)
The reductive degradation of a chlorinated herbicide by iron powder was investigated at lab scale. The studied substrate was triallate (S-2,3,3-trichloroallyl di-isopropyl thiocarbamate) which contains a trichloroethylene moiety potentially reducible by zero-valent iron. Degradation reactions were carried out in batch
Identification of triallate in grain pellets.
T Cairns et al.
Bulletin of environmental contamination and toxicology, 30(2), 234-238 (1983-02-01)

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