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Quinalphos

Quinalphos structure

Quinalphos 

structure
  • CAS No:

    13593-03-8

  • Formula:

    C12H15N2O3PS

  • Chemical Name:

    Quinalphos

  • Synonyms:

    Phosphorothioic acid,O,O-diethyl O-2-quinoxalinyl ester;Bayrusil;O,O-Diethyl O-(quinoxalin-2-yl) thiophosphate;O,O-Diethyl O-(2-quinoxalyl) phosphorothionate;O,O-Diethyl-O-quinoxal-2-yl thionophosphate;SAN 6538;Sandoz 6538;Diethyl 2-quinoxalyl phosphorothionate;Bayer 77049;Quinalphos;BAY 77049;Diethchinalphion;SAN 6626;Sandoz 6626;Ekalux;Quinaltaf;O,O-Diethyl O-2-quinoxalinyl phosphorothioate;Ekalux G5;Diethquinalphion;Quinalfos;Oleoekalux;O,O-Diethyl-O-(2-quinoxalyl)thiophosphate;Kinalux;Ekalux 25EC;Chinalphos;37331-41-2;54511-12-5

  • Categories:

    Agrochemicals  >  Insecticides

Description

Quinalphos is an organic thiophosphate and an organothiophosphate insecticide. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an acaricide and an agrochemical. It derives from a quinoxalin-2-ol.

Quinalphos Basic Attributes

298.3

298.30

237-031-6

26S837727Y

DTXSID7024291

29339900

Characteristics

85.6

3.53

Crystalline

1.306±0.06 g/cm3(Predicted)

31.5 °C

142 °C

2 °C

1.604

In water, 17.8 mg l -1 (22-23 °C)

APPROX 4°C

3.46×10 -4 Pa (20 °C)

Oral-rat LD50: 26 mg/kg; Oral-Mouse LD50: 107 mg/kg

Open flame is flammable; heated to decompose toxic phosphorus oxide, sulfur oxide, nitrogen oxide gas

165.1 Ų [M+H]+ [CCS Type: TW]|168.54 Ų [M-H]-

Safety Information

II

6.1(a)

2783

3

21-25-50/53-51/53-36-20/21/22-11

22-36/37-45-60-61-26

TF6125000

T,N,Xn,F

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

Missing Phrase - N15.00950417-P280-P302 + P352 + P312-P304 + P340 + P310-P305 + P351 + P338 + P310

H300 + H330-H311-H318-H410

|Danger|H301: Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P273, P280, P301+P310, P302+P352, P312, P321, P322, P330, P363, P391, P405, and P501|H301 (98.01%): Toxic if swallowed [Danger Acute toxicity, oral]|P260, P264, P270, P271, P273, P280, P284, P301+P310, P302+P352, P304+P340, P305+P351+P338, P310, P312, P320, P321, P322, P330, P363, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 201 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|P260, P264, P270, P271, P280, P284, P301+P310, P302+P352, P304+P340, P307+P311, P310, P312, P320, P321, P322, P330, P332+P313, P361, P363, P403+P233, P405, and P501|P260, P264, P270, P271, P273, P280, P284, P301+P310, P302+P352, P304+P340, P307+P311, P310, P312, P314, P320, P321, P322, P330, P361, P363, P391, P403+P233, P405, and P501

Toxicity

most 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.)

Bayer 77049

Quinalphos Use and Manufacturing

Methods of Manufacturing

Using o-phenylenediamine, chloroacetic acid and hydrogen peroxide as raw materials, the intermediate 2-hydroxyquinoxaline is prepared, and then condensed with O, O-diethylthiophosphoryl chloride in acetonitrile and potassium carbonate to obtain quinosulfide phosphorus. Raw material consumption quota: 1200kg/t o-phenylenediamine, 1150kg/t chloroacetic acid, 800kg/t O, O-diethylthiophosphoryl chloride.

Uses

Quinalphos is used to control both chewing and sucking insects and mites in a large number of different crops.

Agrochemicals -> Insecticides

Computed Properties

Molecular Weight:298.30
XLogP3:4.4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:298.05410052
Monoisotopic Mass:298.05410052
Topological Polar Surface Area:85.6
Heavy Atom Count:19
Complexity:322
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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