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4383-12-4

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4383-12-4 Usage

Physical State

Colorless liquid

Odor

Sweet, floral

Uses

Production of fragrances
Solvent in various industrial processes

Hazards

Flammable
Skin and eye irritation upon contact

Safety Precautions

Handle and store with proper safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 4383-12-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4383-12:
(6*4)+(5*3)+(4*8)+(3*3)+(2*1)+(1*2)=84
84 % 10 = 4
So 4383-12-4 is a valid CAS Registry Number.

4383-12-4SDS

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 (4-methyl-2-propan-2-ylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-isopropyl-4-methylbenzylalcohol

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:4383-12-4 SDS

4383-12-4Downstream Products

4383-12-4Relevant articles and documents

Kinetics and Regioselectivity of the Autoxidation of o-Substituted Isopropyl Aromatics

Heinze, Antje,Lauterbach, Gerlinde,Pritzkow, Wilhelm,Schmidt-Renner, Wolfgang,Voerckel, Volkmar,Zewegsuren, Nansadyn

, p. 439 - 446 (2007/10/02)

The relative chain propagation constants and the regioselectivities of the oxidations of o-cymene and 2-isopropyl-1,4-dimethylbenzene were determined by competitive oxidations of the hydrocarbons with cumene.As expected, the reactivity of the tertiary C-H bond of the isopropyl group is considerably decreased by o-methyl groups.Also in α-isopropylnaphthalene a considerable decrease in the reactivity of the tertiary C-H bond takes place.The decrease of the chain propagation constants effects a decrease of the oxidabilities of o-substituted isopropyl aromatics.In the case of the methyl isopropyl benzenes the increase of the chain termination constants by primary peroxy radicals must also be taken into consideration.This results in a decrease of the oxidabilities which can be observed even in p-cymene (in comparison with cumene).

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