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Bisultap

Bisultap structure

Bisultap 

structure
  • CAS No:

    52207-48-4

  • Formula:

    C5H13NO6S4.2Na

  • Chemical Name:

    Bisultap

  • Synonyms:

    Thiosulfuric acid (H2S2O3),SS,SS′-[2-(dimethylamino)-1,3-propanediyl] ester,sodium salt (1:2);Thiosulfuric acid (H2S2O3),S,S′-[2-(dimethylamino)-1,3-propanediyl] ester,disodium salt;Disodium 2-dimethylaminopropane-1,3-bisthiosulfonate;Sha Chong Shuang;Dimehypo;Dimehypo jumbo;Bisultap;Thiosultap-sodium;Disosultap;Thiosultap-disodium salt;Molosultap;134716-16-8;28614-68-8

  • Categories:

    Agrochemicals  >  Insecticides

Description

ChEBI: An organic sodium salt that is the disodium salt of thiosultap. An insecticide used to control various pests on rice, vegetable, and fruit trees.


Thiosultap disodium is an organic sodium salt that is the disodium salt of thiosultap. An insecticide used to control various pests on rice, vegetable, and fruit trees. It has a role as an insecticide. It contains a thiosultap(2-).

Bisultap Basic Attributes

355.4

354.926453

2Q555U959O

DTXSID6058394

2930909054

Characteristics

185.00000

1.46500

194-196°C

Oral-Rat  LD50: 451 mg/kg; Oral-Mouse LD50: 130.6 mg/kg

Combustion produces toxic nitrogen oxide and sulfur oxide gas

Safety Information

UN28116.1/PG3

3

21/22-57

36/37

XN6469700

Xn

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

P280-P301 + P310-P312

H301-H311

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P280, P301+P310, P302+P352, P312, P321, P322, P330, P361, P363, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

highly toxic

Drug Information

Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics. (See all compounds classified as Insecticides.)

2-dimethylamino-1,3-bisthiosulfopropane

Bisultap Use and Manufacturing

Methods of Manufacturing

Propylene chloride and dimethylamine are aminated in the presence of sodium hydroxide to prepare N, N-dimethyl allylamine. Then use 30% hydrochloric acid to neutralize to generate hydrochloride. The hydrochloride is chlorinated in chloroform solvent to obtain 1-N, N-dimethyl-2, 3-dichloropropylamine hydrochloride. Finally, it reacts with sodium thiosulfate to synthesize Dimethodium. The reaction product is actually the dimethicone, the dimethicone isomer and their monosodium salt mixture. Due to partial neutralization to pH 6-7, there are actually monosodium salt effective forms and monosodium salt ineffective forms. The above are the main domestic production methods. The Shenyang Research Institute of Chemical Industry and other units have adopted the solvent process technology to improve the quality and yield of Insecticide and reduce the consumption quota.

Uses

The product has been successfully developed on the basis of Shadan. The insecticidal double can be made into insecticidal sheet by acidification. Insecticidal (or Insecticidal) is cyclized with sodium sulfide and salted with oxalic acid to obtain the insecticidal ring. Chilodan, Insecticidal, Insecticidal Ring, Insecticidal Double have the effects of stomach poisoning, contact killing and bone absorption. Insecticidal has excellent control effects on the main pests of various crops such as rice, wheat, corn, beans, vegetables, citrus, fruit trees, tea, forests, etc., such as rice borer, rice borer, rice borer , Rice leaf roll borer, rice blight, leafhopper, rice thrips, negative mud worm, Chinese rice borer, cabbage borer, cabbage worm, yellow stripe, green peach aphid, pear star caterpillar, citrus leaf moth, etc.

Computed Properties

Molecular Weight:355.4
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:5
Exact Mass:354.92646033
Monoisotopic Mass:354.92646033
Topological Polar Surface Area:185
Heavy Atom Count:18
Complexity:327
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

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