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2,5-bis-O-(3-aminopropyl)-1,4:3,6-dianhydrohexitol is a complex organic compound with the molecular formula C12H25NO4. It is a derivative of hexitol, a type of sugar alcohol, with two 3-aminopropyl groups attached to the 2nd and 5th carbon atoms. 2,5-bis-O-(3-aminopropyl)-1,4:3,6-dianhydrohexitol is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The presence of aminopropyl groups allows for further functionalization and the formation of new chemical bonds, making it a versatile building block in organic chemistry.

6338-35-8

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6338-35-8 Usage

Uses

Used in Polymer Synthesis:
2,5-bis-O-(3-aminopropyl)-1,4:3,6-dianhydrohexitol is used as a crosslinking agent in the synthesis of polymer materials. Its ability to form covalent bonds with other molecules contributes to the creation of stable and robust polymer structures, enhancing their mechanical properties and performance in various applications.
Used in Drug Delivery Systems Development:
In the pharmaceutical industry, 2,5-bis-O-(3-aminopropyl)-1,4:3,6-dianhydrohexitol serves as a building block in the development of novel drug delivery systems. Its reactive amino groups allow for the attachment of drug molecules, enabling targeted and controlled release of therapeutic agents. This improves the efficacy and safety of drug administration, particularly for challenging drug molecules.
Used in Biocompatible Materials:
2,5-bis-O-(3-aminopropyl)-1,4:3,6-dianhydrohexitol is also utilized in the development of biocompatible materials for medical applications. Its non-toxic nature and ability to interact with biological systems make it suitable for use in implants, scaffolds, and other medical devices that require direct contact with living tissues.
Overall, 2,5-bis-O-(3-aminopropyl)-1,4:3,6-dianhydrohexitol's unique structure and properties offer a wide range of applications in various industries, with potential for further research and development in creating advanced materials and drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 6338-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6338-35:
(6*6)+(5*3)+(4*3)+(3*8)+(2*3)+(1*5)=98
98 % 10 = 8
So 6338-35-8 is a valid CAS Registry Number.

6338-35-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[[6-(3-aminopropoxy)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3-yl]oxy]propan-1-amine

1.2 Other means of identification

Product number -
Other names N-(2-METHOXYETHYL)-2-[3-(2-METHOXYETHYLCARBAMOYLMETHYL)-1-ADAMANTYL]ACETAMIDE

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:6338-35-8 SDS

6338-35-8Downstream Products

6338-35-8Relevant academic research and scientific papers

DIISOCYANATE COMPOUND HAVING ANHYDROSUGAR ALCOHOL CORE AND PREPARATION METHOD THEREFOR

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Paragraph 0302-0304, (2021/10/11)

The present invention relates to a diisocynate compound having anhydrosugar alcohol core and a preparation method therefor and, more specifically, to a diisocynate compound having anhydrosugar alcohol core and a preparation method therefor, wherein the di

NOVEL FUNCTIONAL COMPOUNDS WITH AN ISOSORBIDE OR ISOSORBIDE ISOMER CORE, PRODUCTION PROCESS AND USES OF THESE COMPOUNDS

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Page/Page column 4, (2010/06/14)

The present invention relates to compounds of formula (I): R—(CH2)2—O-A-O—(CH2)2—R, in which A represents a divalent radical chosen from: and R represents —CN or —CH2NH2. In order to prepare them, acrylonitrile is reacted, via a Michael reaction, with a compound of formula (II): HO-A-OH, in which A is as defined above, in order to obtain a compound of formula (I) in which R represents —CN, and that the hydrogenation of the latter is carried out in order to obtain the corresponding compound of formula (I) in which R represents —CH2NH2. Use is made of a compound of formula (I) in which R represents —CH2NH2 as a polar head in a surfactant, or as a monomer for a condensation polymerization, in particular in the manufacture of polyamides, or else as a crosslinking agents.

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