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134257-64-0

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134257-64-0 Usage

Molecular structure

Hexa-arylbenzene compound with a complex structure

Functional groups

Six 4-methylphenyl groups attached to the benzene ring

Primary use

Curing agent in epoxy resin systems

Other uses

Intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds; antioxidant and additive in lubricants and fuels

Properties

High thermal stability, exceptional electrical and mechanical properties

Industrial applications

Valuable component in various industries due to its properties

Safety concerns

Potential health hazards and toxicity; should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 134257-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,5 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134257-64:
(8*1)+(7*3)+(6*4)+(5*2)+(4*5)+(3*7)+(2*6)+(1*4)=120
120 % 10 = 0
So 134257-64-0 is a valid CAS Registry Number.

134257-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,1-N,3-N,3-N,5-N,5-N-hexakis(4-methylphenyl)benzene-1,3,5-triamine

1.2 Other means of identification

Product number -
Other names 1,3,5-Benzenetriamine,N,N,N',N',N'',N''-hexakis(4-methylphenyl)

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:134257-64-0 SDS

134257-64-0Downstream Products

134257-64-0Relevant articles and documents

One-Shot Multiple Borylation toward BN-Doped Nanographenes

Matsui, Kohei,Oda, Susumu,Yoshiura, Kazuki,Nakajima, Kiichi,Yasuda, Nobuhiro,Hatakeyama, Takuji

, p. 1195 - 1198 (2018)

One-shot double, triple, and quadruple borylation reactions of triarylamines were developed through a judicious choice of boron source and Br?nsted base. With the aid of borylation reactions, a variety of BN-doped nanographenes were synthesized in two steps from commercially available starting materials. An organic light-emitting diode device employing BN-doped nanographene as an emitter exhibited deep pure-blue emission at 460 nm, with CIE coordinates of (0.13, 0.11), and an external quantum efficiency of 18.3%.

Hole-transporting materials for low donor content organic solar cells: Charge transport and device performance

Jiang, Wei,Tao, Chen,Stolterfoht, Martin,Jin, Hui,Stephen, Meera,Lin, Qianqian,Nagiri, Ravi C.R.,Burn, Paul L.,Gentle, Ian R.

, (2019/10/19)

Low donor content solar cells are an intriguing class of photovoltaic device about which there is still considerable discussion with respect to their mode of operation. We have synthesized a series of triphenylamine-based materials for use in low donor co

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