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4468-42-2

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4468-42-2 Usage

Description

(1-Ethylbutyl)benzene, with the chemical formula C12H18, is a colorless liquid that belongs to the alkylbenzene group. It is widely used in industrial processes and is primarily utilized as an intermediate in the production of other chemicals. Classified as a hazardous substance, exposure to high levels can lead to skin and eye irritation, as well as respiratory and central nervous system effects.

Uses

Used in Chemical Production:
(1-Ethylbutyl)benzene is used as an intermediate in the production of other chemicals for various industrial applications.
Used in Solvent Applications:
(1-Ethylbutyl)benzene is used as a solvent in various industrial processes due to its ability to dissolve a wide range of substances.

Check Digit Verification of cas no

The CAS Registry Mumber 4468-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4468-42:
(6*4)+(5*4)+(4*6)+(3*8)+(2*4)+(1*2)=102
102 % 10 = 2
So 4468-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H18/c1-3-8-11(4-2)12-9-6-5-7-10-12/h5-7,9-11H,3-4,8H2,1-2H3

4468-42-2SDS

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 hexan-3-ylbenzene

1.2 Other means of identification

Product number -
Other names Benzene, (1-ethylbutyl)-

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:4468-42-2 SDS

4468-42-2Relevant articles and documents

A New Preparation Method for the Alkylation Catalysts of Aromatic Compounds Based on Immobilized AlCl3

Bykov,Belyaev

, p. 328 - 330 (2021/04/26)

Abstract: A new method for the preparation of active catalysts for the alkylation and transalkylation of aromatic compounds (benzene and toluene) based on aluminum chloride immobilized on the surface of silica gel was developed. The alkylation occurred wi

Use of Trifluoromethyl Groups for Catalytic Benzylation and Alkylation with Subsequent Hydrodefluorination

Zhu, Jiangtao,Prez, Manuel,Caputo, Christopher B.,Stephan, Douglas W.

supporting information, p. 1417 - 1421 (2016/02/14)

The electrophilic organofluorophosphonium catalyst [(C6F5)3PF][B(C6F5)4] is shown to effect benzylation or alkylation by aryl and alkyl CF3 groups with subsequent hydrodefluorination, thus resulting in a net transformation of CF3 into CH2-aryl fragments. In the case of alkyl CF3 groups, Friedel-Crafts alkylation by the difluorocarbocation proceeded without cation rearrangement, in contrast to the corresponding reactions of alkyl monofluorides.

N-Hexane activation over zeolites: Aromatic alkylation to 1-phenylhexane

Danilina, Nadiya,Payrer, Elisabeth L.,Van Bokhoven, Jeroen A.

scheme or table, p. 1509 - 1510 (2010/06/12)

Terminal 1-phenylhexane was observed during alkylation of benzene with n-hexane over 10-membered ring zeolites at moderate temperature, whereas it was not observed when 1-hexene was the reactant. The Royal Society of Chemistry 2010.

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