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1,5-Bis(4-aminophenoxy)pentane is an organic compound with the chemical formula C17H22N2O2. It is a colorless, crystalline solid that is soluble in organic solvents such as ethanol and acetone. 1,5-BIS(4-AMINOPHENOXY)PENTANE is primarily used as a monomer in the synthesis of polyetherimide polymers, which are known for their high thermal stability, mechanical strength, and chemical resistance. These polymers find applications in various industries, including aerospace, automotive, and electronics, where high-performance materials are required. The compound is also used in the production of certain types of adhesives and coatings. Due to its potential health and environmental risks, it is important to handle 1,5-bis(4-aminophenoxy)pentane with care, following proper safety guidelines.

1092-82-6

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1092-82-6 Usage

Structure

Pentane backbone with two 4-aminophenoxy (4-AP) groups attached at the first and fifth carbon positions

Applications

a. Curing agent in epoxy resins
b. Crosslinking agent in polyurethane production
c. Intermediate in pharmaceutical synthesis

Properties

a. Enhances mechanical properties of polymers
b. Improves thermal stability of polymers

Safety precautions

Skin and eye irritant; proper protective measures should be taken when handling

Check Digit Verification of cas no

The CAS Registry Mumber 1092-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1092-82:
(6*1)+(5*0)+(4*9)+(3*2)+(2*8)+(1*2)=66
66 % 10 = 6
So 1092-82-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H20N2O2/c18-14-8-6-12-4-2-1-3-5-13-7-9-15(19)17(11-13)21-20-16(14)10-12/h6-11H,1-5,18-19H2

1092-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-pentanediyldioxy-di-aniline, dihydrochloride

1.2 Other means of identification

Product number -
Other names 4,4'-Pentandiyldioxy-di-anilin, Dihydrochlorid

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:1092-82-6 SDS

1092-82-6Relevant academic research and scientific papers

Biological properties of amidinium sulfinic and sulfonic acid derivatives: inhibition of glycolytic enzymes of Trypanosoma brucei and protective effect on cell growth

Willson, M,Perie, JJ,Malecaze, F,Opperdoes, F,Callens, M

, p. 799 - 808 (2007/10/02)

The activity of the title compounds has been investigated on two biological targets: cultures of trypanosome and glycolytic enzymes inhibition of the parasite, and on retinal epithelium cells.In both cases, these compounds exhibit a significant activity,

MESOGENIC POLYMERS. 6. TWO SERIES OF ISOMERIC POLYAZOMETHINES.

Griffin,Britt,Hung,Steele

, p. 305 - 314 (2007/10/02)

Two homologoous series of alternating rigid-flexible, main chain liquid crystalline polyimines are reported; one based on terephthaldehyde the other based on p-phenylenediamine. It was found through examination of optical microscopic, x-ray diffraction an

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