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S-ethyl piperidine-1-carbothioate, also known as EPTC, is a selective pre-emergence herbicide belonging to the thiocarbamate class. It is primarily used to control a wide range of annual grasses and broadleaf weeds in various crops, including cotton, soybeans, and corn. EPTC works by inhibiting the growth of weeds by disrupting their photosynthesis process, ultimately leading to their death. It is absorbed by the plant's roots and is considered less toxic to mammals and birds compared to other herbicides. However, it is essential to follow proper application guidelines to minimize potential environmental and health risks.

6961-73-5

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6961-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6961-73-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6961-73:
(6*6)+(5*9)+(4*6)+(3*1)+(2*7)+(1*3)=125
125 % 10 = 5
So 6961-73-5 is a valid CAS Registry Number.

6961-73-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name S-Ethyl-N,N-pentamethylen-thiocarbamat

1.2 Other means of identification

Product number -
Other names Piperidin-1-thiocarbonsaeure-S-aethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6961-73-5 SDS

6961-73-5Downstream Products

6961-73-5Relevant academic research and scientific papers

The Synthesis of Alkyl Thiocarbamates in an Ultrasonic Field

Galiakhmetov, R. N.,Valitov, R. B.,Kurochkin, A. K.,Margulis, M. A.

, p. 614 - 615 (2007/10/02)

The synthesis of alkylthiocarbamates from an alkali metal salt of thiocarbamic acid and halogenohydrocarbons in an aqueous medium has been investigated with exposure to ultrasound and without such exposure but under conditions of vigorous stirring.The intensifying effect of ultrasound on the synthesis thiocarbamates has been demonstrated.

Process for the preparation of substituted S-alkyl thio-carbamates

-

, (2008/06/13)

The invention relates to a new and advantageous process for the preparation of substituted S-alkyl thiocarbamates having the general formula (I), EQU1 wherein R1 stands for a C1-4 alkyl group, R2 stands for a C1-4 alkyl or cyclohexyl group, or R1 and R2 may form together a C4-6 polymethylene group, and R3 stands for a C2-3 alkyl group. In accordance with the invention the substituted O-alkyl thiocarbamates of the general formula (II), EQU2 wherein R1, R2 and R3 each have the same meanings as defined above, are subjected to isomerization by heating them at a temperature of 130° to 180°C in the presence of dimethyl sulfate or diethyl sulfate to yield the appropriate S-alkyl esters.

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