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TETRASUL is a chlorinated diphenyl sulfide acaricide, specifically designed for the control of mites and other pests in various crops. It is an effective and widely used chemical compound in the agricultural and gardening industries to protect plants from harmful pests, ensuring a healthy and productive yield.

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  • 2227-13-6 Structure
  • Basic information

    1. Product Name: TETRASUL
    2. Synonyms: 2,4,4',5-TETRACHLORODIPHENYLSULPHIDE;TETRASUL;1,2,4-trichloro-5-((4-chlorophenyl)thio)-benzen;2,4,4’,5-tetrachlorodiphenylsulfide;2,4,5,4’-tetrachlorodiphenylsulfide;3,4,6,4’-tetrachlor-diphenylsulfid;4-chlorophenyl2,4,5-trichlorophenylsulfide;animert
    3. CAS NO:2227-13-6
    4. Molecular Formula: C12H6Cl4S
    5. Molecular Weight: 324.05
    6. EINECS: 218-761-4
    7. Product Categories: N/A
    8. Mol File: 2227-13-6.mol
  • Chemical Properties

    1. Melting Point: 84-85 °C
    2. Boiling Point: 408.1 °C at 760 mmHg
    3. Flash Point: 185.9 °C
    4. Appearance: /
    5. Density: 1.4963 (estimate)
    6. Vapor Pressure: 1.69E-06mmHg at 25°C
    7. Refractive Index: 1.678
    8. Storage Temp.: 0-6°C
    9. Solubility: Chloroform (Soluble), Dichloromethane (Slightly)
    10. CAS DataBase Reference: TETRASUL(CAS DataBase Reference)
    11. NIST Chemistry Reference: TETRASUL(2227-13-6)
    12. EPA Substance Registry System: TETRASUL(2227-13-6)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 21-52
    3. Safety Statements: 36
    4. WGK Germany:
    5. RTECS: WQ3850000
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2227-13-6(Hazardous Substances Data)

2227-13-6 Usage

Uses

Used in Agricultural Industry:
TETRASUL is used as a miticide for controlling mites and other pests in food and gardening crops. It helps in protecting the plants from damage caused by these pests, leading to a better yield and improved quality of the produce.
Used in Gardening Industry:
In the gardening industry, TETRASUL is used as an acaricide to manage and control mite infestations in ornamental plants and gardens. It ensures the health and beauty of the plants by preventing damage caused by mites and other related pests.

Check Digit Verification of cas no

The CAS Registry Mumber 2227-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2227-13:
(6*2)+(5*2)+(4*2)+(3*7)+(2*1)+(1*3)=56
56 % 10 = 6
So 2227-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H6Cl4S/c13-7-1-3-8(4-2-7)17-12-6-10(15)9(14)5-11(12)16/h1-6H

2227-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tetrasul

1.2 Other means of identification

Product number -
Other names 1,2,4-trichloro-5-[(4-chlorophenyl)sulfanyl]benzene

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:2227-13-6 SDS

2227-13-6Downstream Products

2227-13-6Relevant articles and documents

Synthesis of Cl2- to Cl4-diphenylsulfides and Cl1- to Cl3-dibenzothiophenes

Sielex, Klaus,Andersson, Jan T.

, p. 3529 - 3539 (2007/10/03)

The synthesis of eleven environmentally relevant mono-, di- and trichlorodibenzothiophenes (2) by photochemical ring-closure of polychlorodiphenylsulfides (1) is described. All monochlorodibenzothiophenes were additionally synthesized starting with a chlorothiophenol in a three-step reaction adapted from the synthesis of methyldibenzothiophenes.

Preparation of organic sulfone compounds

-

, (2008/06/13)

An in-situ process for preparing organic sulfone compounds by oxidizing the corresponding sulfide compound with a mixture of hydrogen peroxide, a carboxylic acid in the presence of a catalytic amount of a mineral acid or an organic sulfonic acid.

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