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1,10-Bis(4-hydroxydiphenoxy)decane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70856-53-0

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70856-53-0 Usage

Family

Bisphenols

Use

Widely used in the production of plastics and resins

Structure

Long carbon chain with two hydroxydiphenoxy groups attached at the 1st and 10th positions

Commonly used in

Building block in the production of high-performance thermoplastics, such as polyetherimide and polysulfone

Health risks

Potential endocrine disrupting properties and suspected carcinogen

Environmental impact

Persists in the environment and has been detected in various water bodies

Ongoing research

Debate about the regulation and safety of this chemical in various consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 70856-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,5 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70856-53:
(7*7)+(6*0)+(5*8)+(4*5)+(3*6)+(2*5)+(1*3)=140
140 % 10 = 0
So 70856-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H30O4/c23-19-9-13-21(14-10-19)25-17-7-5-3-1-2-4-6-8-18-26-22-15-11-20(24)12-16-22/h9-16,23-24H,1-8,17-18H2

70856-53-0SDS

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 4-[10-(4-hydroxy-2-phenoxyphenoxy)decoxy]-3-phenoxyphenol

1.2 Other means of identification

Product number -
Other names 4,4'-dihydroxy-1,10-diphenoxydecane

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:70856-53-0 SDS

70856-53-0Relevant academic research and scientific papers

Acyclic cucurbit[n]urils capped with alkylene linkers: synthesis and molecular recognition properties

Ganapati, Shweta,Isaacs, Lyle

, p. 114 - 126 (2018/11/02)

We report the synthesis and characterization of three new acyclic cucurbit[n]uril-type receptors that feature a covalent capping group in the form of an alkylene linker (2a–2c) that we hypothesized would have higher binding affinity toward alkylammonium i

Relationship between conformational flexibility and chelate cooperativity

Misuraca, M. Cristina,Grecu, Tudor,Freixa, Zoraida,Garavini, Valentina,Hunter, Christopher A.,Van Leeuwen, Piet W.N.M.,Segarra-Maset, M. Dolores,Turega, Simon M.

experimental part, p. 2723 - 2732 (2011/06/21)

A family of four biscarbamates (AA) and four bisphenols (DD) were synthesized, and H-bonding interactions between all AA?DD combinations were characterized using 1H NMR titrations in carbon tetrachloride. A chemical double mutant cycle analysis

PREPARATION AND PROPERTIES OF OLIGOMERS OF DEFINED CHAIN LENGTH AND STRUCTURE AS MODELS FOR TECHNICAL COPOLYMERS

Seliger, H.,Bitar, M. B.,Goeldner, E.,Kittel, I.,Kilian, H. G.

, p. 171 - 186 (2007/10/03)

Oligomeric segments of the macromolecules with defined structure have been prepared in an attempt to answer the question whether the thermal and mechanical properties of the elastomers (polyester) are mainly influenced by the segregation or by the structu

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