| Identification | Back Directory | [Name]
ETHIOLATE | [CAS]
2941-55-1 | [Synonyms]
VEER
ETHIO
CHEMIT
etirox
Prefox
S-15076
NILMITE
ETHOSAN
DHANUMIT
ETHIOLAT
ACITHION
TOMAHAWK
ETHIOLATE
DEVIASTRA
WARIWGPBHKPYON-UHFFFAOYSA-N
5-ETHYL DIETHYLTHIOCARBAMATE
s-ethyldiethylcarbamothioate
S-ethyl diethylthiocarbamate
ethiolate (ansi,bsi,iso,wssa)
s-ethyl n,n-diethylthiocarbamate
Ethiolat@100 μg/mL in Acetonitrile
diethylthio-carbamicacis-ethylester
N,N-diethyl(ethylsulfanyl)formamide
diethyl-carbamothioicacis-ethylester
Diethylthiocarbamic acid S-ethyl ester
Ethiolate Solution in Methanol, 100μg/mL
ETHIOLAT PESTANAL (S-ETHYL N,N-DI- ETHYL
N,N-Diethylthiocarbamic acid S-ethyl ester
Carbamothioic acid, N,N-diethyl-, S-ethyl ester | [Molecular Formula]
C7H15NOS | [MDL Number]
MFCD00055308 | [MOL File]
2941-55-1.mol | [Molecular Weight]
161.27 |
| Chemical Properties | Back Directory | [Boiling point ]
215.6±23.0 °C(Predicted) | [density ]
0.99 g/mL at 20 °C | [refractive index ]
1.6370 (estimate) | [storage temp. ]
APPROX 4°C
| [form ]
neat | [pka]
-1.22±0.70(Predicted) | [BRN ]
1755151 | [Major Application]
agriculture
environmental | [InChI]
1S/C7H15NOS/c1-4-8(5-2)7(9)10-6-3/h4-6H2,1-3H3 | [InChIKey]
WARIWGPBHKPYON-UHFFFAOYSA-N | [SMILES]
CCSC(=O)N(CC)CC | [EPA Substance Registry System]
Ethiolate (2941-55-1) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
22 | [RIDADR ]
2902 | [WGK Germany ]
3 | [RTECS ]
EZ7290000 | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
29302000 | [Storage Class]
12 - Non Combustible Liquids | [Hazard Classifications]
Acute Tox. 4 Oral | [Toxicity]
rat,LD50,oral,400mg/kg (400mg/kg),Farm Chemicals Handbook. Vol. -, Pg. C247, 1991. |
| Hazard Information | Back Directory | [Uses]
S-ethyl Ester N,N-Diethyl-carbamothioic Acid, is a herbiside and also a pesticide that has been found in avocados. | [Definition]
ChEBI: Ethiolate is a tertiary amine. | [Production Methods]
The commercial production route of ethiolate is not documented in open literature. However, based on its chemical identity its commercial synthesis would have followed the same well established thiocarbamate route used for related herbicides: reacting diethylamine with carbon disulphide to form the corresponding diethyl dithiocarbamate salt, then alkylating this intermediate with ethyl halide (typically ethyl chloride or ethyl bromide) to yield the S-ethyl thiocarbamate ester. | [Mechanism of action]
Selective, inhibits lipid metabolism and thus the development of seedling shoots and roots | [Pesticide Type]
Herbicide |
|
| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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