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N,N'-Di-N-butyl-1,6-hexanediamine is an organic compound with the chemical formula C14H32N2. It is a colorless to pale yellow liquid at room temperature and is soluble in water. This chemical is primarily used as a curing agent for epoxy resins, enhancing their mechanical properties and thermal stability. It is also employed as a crosslinking agent in various polymers, contributing to improved adhesion and flexibility. Due to its amine groups, it can react with isocyanates and other reactive groups, making it a versatile component in the production of polyurethanes, coatings, and elastomers. The compound is synthesized by the reaction of 1,6-hexanediamine with butylamine, and its use in industrial applications is governed by safety regulations due to its potential health and environmental impacts.

4835-11-4

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4835-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4835-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4835-11:
(6*4)+(5*8)+(4*3)+(3*5)+(2*1)+(1*1)=94
94 % 10 = 4
So 4835-11-4 is a valid CAS Registry Number.

4835-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-dibutylhexane-1,6-diamine

1.2 Other means of identification

Product number -
Other names 1,6-N,N'-Dibutylhexanediamine

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:4835-11-4 SDS

4835-11-4Downstream Products

4835-11-4Relevant academic research and scientific papers

Use of additive sites to control nitric oxide release from nitric oxide donors contained within polymers

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Page/Page column 6; 9; 12, (2008/06/13)

A method for increasing, prolonging, and/or controlling the release rates of nitric oxide (NO) from polymeric materials containing NO adducts. Such NO-containing polymeric materials may find use in devices such as blood contacting devices, and biocompatible devices utilizing the same. The method and device utilizes anionic site additives, acidic site additives and/or acidic producing site additives in a polymer that contains NO-adducts to generate higher fluxes of NO to exceed NO threshold levels desirable to substantially prevent and/or minimize reactions such as platelet activation or adhesion.

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