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Dimepiperate

Dimepiperate structure

Dimepiperate 

structure
  • CAS No:

    61432-55-1

  • Formula:

    C15H21NOS

  • Chemical Name:

    Dimepiperate

  • Synonyms:

    1-Piperidinecarbothioic acid,S-(1-methyl-1-phenylethyl) ester;MY 93;Dimepiperate;MUW 1193;Yukamate

  • Categories:

    Agrochemicals  >  Herbicides

Description

Dimepiperate is a monothiocarbamic ester and a piperidinecarboxylate ester.

Dimepiperate Basic Attributes

263.4

263.40

262-784-2

3WIT88R79X

DTXSID5058141

29333990

Characteristics

45.6

4.19870

1.109g/cm3

39 °C

166 °C

180.6ºC

1.563

7.59e-05 M

0-6°C

4.00e-06 mmHg

Oral-Rat LD50: 946 mg/kg; Oral-Mouse LD50: 4519 mg/kg

Combustion produces toxic nitrogen oxide and sulfur oxide gas

Safety Information

UN30829/PG3

3

22-51/53

61

TM5958000

Xn,N

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

P273

H302-H411

|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P301+P312, P330, P391, and P501|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|P264, P270, P301+P312, P330, and P501

Toxicity

moderately toxic

Dimepiperate Use and Manufacturing

Methods of Manufacturing

g toluene or piperidine as the solvent, add α, α-dimethylbenzyl mercaptan, then add dropwise 40% sodium hydroxide solution at room temperature, reflux for reaction, and separate the water. The temperature is raised to 60-70°C, piperidinecarboxylic acid chloride is added dropwise, the precipitated sodium chloride is filtered off, the temperature is raised to react for several hours, and piperidine is obtained after washing with water, drying and desolventizing. The synthesis method of α, α-dimethylbenzyl mercaptan is as follows: 1, 4-dioxane is used as a solvent, and α-methylstyrene and hydrogen sulfide are reacted in the presence of a catalyst. The yield is 86.3%. Dimethyl sulfoxide can also be used as a solvent, the corresponding nitro compound is treated with Na2S2, and the resultant is prepared by reacting with aluminum amalgam at 0°C, with a yield of 92%.

Uses

Systemic conductivity selective herbicide in paddy field. It has outstanding effect on controlling barnyard grass before the 2nd leaf stage. The agent is absorbed by the root system, stem, and leaves and then transmitted to the entire plant, breaking the balance of endogenous auxin, thereby inhibiting intracellular protein synthesis, disrupting the division of growth point cells, and inhibiting and delaying the formation of weed stems and leaves, growth and development Stop, the stems and leaves change from thick green to yellow, brown to die. For example, after the emergence of rice dry farming, barnyardgrass 1.5-2.5 leaf stage, per 100 square meters with piperazine 50% emulsifiable concentrate 30mL plus 20% diarrhea emulsifiable concentrate 75 ~ 112.6mL, 4.5 ~ 6kg water, stem and leaf spray. Before and after sowing, dry and wet seedlings are sprayed with 50% emulsifiable concentrate 22.5-30mL per 100 square meters and sprayed with 3.75~4.5kg of water on the bed surface. The water-cultivated seedlings can be applied by poisonous soil method 1-4d after sowing . In the transplanting field, spray water with 22.5 to 39 mL of 50% emulsifiable concentrate 3 to 7 days after transplanting. After application, keep a 3 to 5 cm water layer for 5 to 7 days. When there are many types of weeds in paddy fields, they should be mixed with other herbicides.

Agrochemicals -> Herbicides

Computed Properties

Molecular Weight:263.4
XLogP3:3.6
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:263.13438547
Monoisotopic Mass:263.13438547
Topological Polar Surface Area:45.6
Heavy Atom Count:18
Complexity:278
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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