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1,3,5-Tris(dibromomethyl)benzene, with the molecular formula C9H9Br3, is a colorless to pale yellow liquid at room temperature. It is insoluble in water and is recognized for its flame retardant properties.

1889-66-3

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1889-66-3 Usage

Uses

Used in Textile Industry:
1,3,5-Tris(dibromomethyl)benzene is used as a flame retardant in textiles to enhance their fire resistance. It releases bromine radicals at high temperatures, which react with the free radicals in the flame, thereby inhibiting the combustion process.
Used in Plastics Industry:
In the plastics industry, 1,3,5-Tris(dibromomethyl)benzene is utilized as a flame retardant to improve the fire safety of plastic materials. Its chemical reaction with flame radicals helps to slow down or prevent the spread of fire.
Used in Electronic Devices:
1,3,5-Tris(dibromomethyl)benzene is employed in electronic devices as a flame retardant to reduce the risk of fire hazards. Its ability to release bromine radicals upon exposure to heat aids in controlling the combustion process within electronic components.
However, due to its identification as a persistent organic pollutant, 1,3,5-Tris(dibromomethyl)benzene has raised environmental and health concerns. Its toxicity and potential for bioaccumulation have led to restrictions or bans on its use in certain countries, highlighting the need for safer alternatives in flame retardant applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1889-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1889-66:
(6*1)+(5*8)+(4*8)+(3*9)+(2*6)+(1*6)=123
123 % 10 = 3
So 1889-66-3 is a valid CAS Registry Number.

1889-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Tris(dibromomethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,3,5-Tris(dibrommethyl)benzol

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:1889-66-3 SDS

1889-66-3Upstream product

1889-66-3Relevant academic research and scientific papers

A C3-symmetric colorimetric anion sensor bearing hydrazone groups as binding sites

Shao, Jie,Qiao, Yanhong,Lin, Hai,Lin, Huakuan

, p. 1736 - 1740 (2009)

Tris-hydrazone (1) functioned as a colorimetric chemosensor for a variety of anions such as F-, AcO- and H2PO4-. The anion binding could be easily detected by naked-eye according to color changes. The high binding ability of the receptor 1 to anions was further investigated by UV-vis absorption spectroscopy in DMSO. The results of job plot of the receptor 1 with different anions demonstrated that the stoichiometry of the complex between 1 and F- was 1:1 (1:anion) and the stoichiometry of the other complexes studied was 1:3 (1:anion).

Synthesis and mesomorphic properties of new columnar liquid crystal containing 1,3,5-triiminebenzene with pendant 1,3,4-thiadiazole Group

Al-Malki, Mustafa K.S.,Hameed, Ayad S.,Al-Dujaili, Ammar H.

, p. 34 - 42 (2014/07/07)

A novel discotic liquid crystal series based on 1,3,5-benzenetrisazomethine derivatives with three pendant 2-amino-5-(4′-n-alkoxy)phenyl-1,3,4- thiadiazole has been synthesized, which is the first columnar molecules containing 1,3,4-thiadiazole moiety exhibiting a discotic liquid crystal. The molecular structure of compounds was confirmed by FT-IR, 1H-NMR, and mass spectroscopy and elemental analysis. The electron excitation properties of these compounds were investigated by UV-vis absorption spectroscopy. Their liquid crystalline properties were studied by polarizing optical microscopy and differential scanning calorimetry. The formation of a columnar mesophase was found to be dependent on the number of methylene unit in alkoxy side chains.

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