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2,4,5,6,7-PENTABROMO-1H-BENZOIMIDAZOLE is a chemical compound that is widely recognized for its flame retardant properties. It is a member of the brominated flame retardants, which are utilized to diminish the flammability of various materials, thereby aiding in the prevention of fire spread. Despite its effectiveness, there is significant concern regarding its environmental persistence, bioaccumulation in organisms, and potential toxicological effects on both human health and wildlife. As a result, regulatory measures have been implemented in numerous countries to restrict or ban its usage.

16865-25-1

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16865-25-1 Usage

Uses

Used in Electronics Industry:
2,4,5,6,7-PENTABROMO-1H-BENZOIMIDAZOLE is used as a flame retardant additive in the electronics industry to enhance the fire safety of electronic devices and components. Its application helps to slow down the combustion process and reduce the risk of fire-related accidents.
Used in Textile Industry:
In the textile industry, 2,4,5,6,7-PENTABROMO-1H-BENZOIMIDAZOLE is used as a flame retardant in fabrics and materials to improve their resistance to fire. This is particularly important for products that come into contact with high temperatures or are used in environments with increased fire risk.
Used in Building Materials:
2,4,5,6,7-PENTABROMO-1H-BENZOIMIDAZOLE is utilized as a flame retardant in building materials to reduce the flammability of construction products such as insulation, wall coverings, and upholstery. This helps to improve the overall fire safety of buildings and protect occupants in the event of a fire.
However, due to the growing awareness of the potential health and environmental impacts of 2,4,5,6,7-PENTABROMO-1H-BENZOIMIDAZOLE, there is a shift towards finding safer alternatives for flame retardancy in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 16865-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,6 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16865-25:
(7*1)+(6*6)+(5*8)+(4*6)+(3*5)+(2*2)+(1*5)=131
131 % 10 = 1
So 16865-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C7HBr5N2/c8-1-2(9)4(11)6-5(3(1)10)13-7(12)14-6/h(H,13,14)

16865-25-1SDS

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 2,4,5,6,7-pentabromo-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazole,2,4,5,6,7-pentabromo

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:16865-25-1 SDS

16865-25-1Relevant academic research and scientific papers

From a MMP2/CK2 multitarget approach to the identification of potent and selective MMP13 inhibitors

Pastor, Miryam,Zapico, José María,Coderch, Claire,Maslyk, Maciej,Panchuk, Rostyslav,De Pascual-Teresa, Beatriz,Ramos, Ana

, p. 916 - 929 (2019/01/30)

In this article, we describe our efforts in the search of MMP2/CK2 dual targeting inhibitors. We have followed a rational drug design approach based on our experience in the selective inhibition of these two enzymes. We have successfully obtained highly a

Polyhalogenobenzimidazoles: Synthesis and their inhibitory activity against casein kinases

Andrzejewska, Mariola,Pagano, Mario A.,Meggio, Flavio,Brunati, Anna Maria,Kazimierczuk, Zygmunt

, p. 3997 - 4002 (2007/10/03)

A series of novel polyhalogenated benzimidazoles have been prepared by exhaustive bromination of a variety of 2-substituted benzimidazoles. The efficacy of both new compounds and a number of their previously described cognates as inhibitors of casein kinases CK1, CK2 and G-CK was investigated. The type of N-1 alkyl substituent as well as introduction of a polyfluoroalkyl moiety at position 2 did not markedly influence the inhibitory efficacy toward CK2 of the respective 4,5,6,7-tetrabromobenzimidazole derivatives which conversely were almost ineffective toward CK1 and G-CK. However, 4,5,6,7-tetrabromobenzimidazoles substituted at position 2 with either chlorine, bromine or sulfur atom, while manifesting a still considerable inhibitory activity against CK2 (IC50 in the 0.49-0.93 μM range) proved to be potentially powerful inhibitors also against CK1 (IC50 in the 18.4-2.2 μM range).

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