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2,3,4,5-tetrabromo-6-chlorotoluene, also known as Tetrabromo-o-chlorotoluene, is an organic compound characterized by its tetrabromo and chloro substitutions on the toluene molecule. It is a halogenated aromatic compound known for its flame retardant properties and is also utilized as a standard in environmental testing and research.

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  • 39569-21-6 Structure
  • Basic information

    1. Product Name: 2,3,4,5-tetrabromo-6-chlorotoluene
    2. Synonyms: 2,3,4,5-tetrabromo-6-chlorotoluene;1,2,3,4-Tetrabromo-5-chloro-6-methylbenzene
    3. CAS NO:39569-21-6
    4. Molecular Formula: C7H3Br4Cl
    5. Molecular Weight: 442.16772
    6. EINECS: 254-522-0
    7. Product Categories: N/A
    8. Mol File: 39569-21-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 379.3°Cat760mmHg
    3. Flash Point: 198.1°C
    4. Appearance: /
    5. Density: 2.424g/cm3
    6. Vapor Pressure: 1.29E-05mmHg at 25°C
    7. Refractive Index: 1.652
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3,4,5-tetrabromo-6-chlorotoluene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3,4,5-tetrabromo-6-chlorotoluene(39569-21-6)
    12. EPA Substance Registry System: 2,3,4,5-tetrabromo-6-chlorotoluene(39569-21-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 39569-21-6(Hazardous Substances Data)

39569-21-6 Usage

Uses

Used in Flame Retardancy:
2,3,4,5-tetrabromo-6-chlorotoluene is used as an additive in the plastics and polymer industry for its flame retardant properties. 2,3,4,5-tetrabromo-6-chlorotoluene's high bromine and chlorine content contribute to its effectiveness in reducing the flammability of materials, making it a valuable component in the production of fire-resistant products.
Used in Environmental Testing and Research:
In the field of environmental science, 2,3,4,5-tetrabromo-6-chlorotoluene serves as a standard reference material for testing and research purposes. Its well-defined chemical structure and properties make it suitable for calibrating analytical instruments and methodologies, ensuring accurate measurements and assessments in environmental monitoring and hazard identification.

Check Digit Verification of cas no

The CAS Registry Mumber 39569-21-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,6 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39569-21:
(7*3)+(6*9)+(5*5)+(4*6)+(3*9)+(2*2)+(1*1)=156
156 % 10 = 6
So 39569-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Br4Cl/c1-2-3(8)4(9)5(10)6(11)7(2)12/h1H3

39569-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrabromo-5-chloro-6-methylbenzene

1.2 Other means of identification

Product number -
Other names 2,3,4,5-Tetrabrom-6-chlor-toluol

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:39569-21-6 SDS

39569-21-6Upstream product

39569-21-6Downstream Products

39569-21-6Relevant articles and documents

Polyhalobenzylic disulfooxonium compounds

-

, (2008/06/13)

Polyhalobenzylic disulfooxonium compounds are produced by the reaction of aromatic methyl, halomethyl or hydroxymethyl substituents with sulfur trioxide. The disulfooxonium salts are readily converted to alcohols by hydrolysis to provide monomers for the production of fire resistant polymers and additives for polymers. Likewise, the disulfooxonium compounds of this invention present chemical intermediates for a wide range of useful products such as halogenated pesticides.

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