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1-Hexanol, 6-[3,5-bis(methoxymethyl)-2,4,6-trimethylphenoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

823816-13-3

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823816-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 823816-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,8,1 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 823816-13:
(8*8)+(7*2)+(6*3)+(5*8)+(4*1)+(3*6)+(2*1)+(1*3)=163
163 % 10 = 3
So 823816-13-3 is a valid CAS Registry Number.

823816-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[3,5-bis(methoxymethyl)-2,4,6-trimethylphenoxy]hexan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Hexanol,6-[3,5-bis(methoxymethyl)-2,4,6-trimethylphenoxy]

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:823816-13-3 SDS

823816-13-3Downstream Products

823816-13-3Relevant academic research and scientific papers

Hyperbranched copolymers versus linear copolymers: A comparative study of thermal properties

Behera, Girish Ch.,Saha, Animesh,Ramakrishnan

, p. 7695 - 7701 (2008/02/02)

Copolymerization of two AB2-type monomers that incorporate spacer segments of similar lengths but different flexibility permitted, for the first time, the preparation of a range of hyperbranched copolymers, wherein the backbone rigidity was varied while maintaining similar branching densities. The copolymers were prepared via a recently developed melt transetherification methodology to yield moderately high molecular weight polymers, with molecular weights ranging from 20 000 to 50 000. 1H NMR spectroscopic studies revealed that the composition of the copolymers varied linearly with monomer composition, confirming the formation of truly random copolymers. Analogous linear copolymers based on suitably designed AB-type monomers, containing the same two spacers, were also prepared for comparison. Thermal analysis of these copolymers using DSC indicated that the Tg's of both linear copolymers and hyperbranched copolymers varied with composition in a manner that was in complete accordance with the Fox equation, although all the linear copolymers exhibited significantly higher Tg values than their hyperbranched counterparts. It is interesting that, despite their very different topology and the presence of large number of chain ends, hyperbranched copolymers exhibit a similar Tg variation as their linear analogues. The generality of this observation in the broader context of hyperbranched copolymers, such as those possessing different branching densities and terminal functionalities, remains to be tested.

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