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N,N-dipropylpropane-1,3-diamine, also known as DIPA, is an organic compound with the chemical formula C9H21N. It is a colorless liquid with a slight amine odor and is soluble in water. This chemical is primarily used as a curing agent for epoxy resins, enhancing the mechanical properties and chemical resistance of the resulting polymer. It is also employed as a crosslinking agent in various applications, such as coatings, adhesives, and composite materials. Due to its amine nature, it can react with epoxy groups to form strong, durable bonds. N,N-dipropylpropane-1,3-diamine is known for its high reactivity and is often preferred for its ability to provide excellent adhesion and flexibility in the final product.

6345-82-0

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6345-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6345-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6345-82:
(6*6)+(5*3)+(4*4)+(3*5)+(2*8)+(1*2)=100
100 % 10 = 0
So 6345-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H22N2/c1-3-7-11(8-4-2)9-5-6-10/h3-10H2,1-2H3

6345-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N',N'-dipropylpropane-1,3-diamine

1.2 Other means of identification

Product number -
Other names 3-Dipropylamino-propylamin

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:6345-82-0 SDS

6345-82-0Relevant academic research and scientific papers

Parallel synthesis of 9-aminoacridines and their evaluation against chloroquine-resistant Plasmodium falciparum

Anderson, Marc O.,Sherrill, John,Madrid, Peter B.,Liou, Ally P.,Weisman, Jennifer L.,DeRisi, Joseph L.,Guy, R. Kiplin

, p. 334 - 343 (2007/10/03)

A parallel synthetic strategy to the 9-aminoacridine scaffold of the classical anti-malarial drug quinacrine (2) is presented. The method features a new route to 9-chloroacridines that utilizes triflates of salicylic acid derivatives, which are commercially available in a variety of substitution patterns. The route allows ready variation of the two diversity elements present in this class of molecules: the tricyclic aromatic heterocyclic core, and the disubstituted diamine sidechain. In this study, a library of 175 compounds was designed, although only 93 of the final products had purities acceptable for screening. Impurity was generally due to incomplete removal of 9-acridones (18), a degradation product of the 9-chloroacridine synthetic intermediates. The library was screened against two strains of Plasmodium falciparum, including a model of the drug-resistant parasite, and six novel compounds were found to have IC50 values in the low nanomolar range.

AMINE COMPOUNDS AND USE THEREOF

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Page/Page column 45-46, (2010/02/12)

It is intended to provide novel amine compounds which are efficacious against diseases such as infection with HIV virus, rheumatism and cancer metastasis. Namely, amine compounds represented by the following general formula (1):In a typical case, A1 and A2 represent each an optionally substituted monocyclic or polycyclic aromatic heterocycle; W represents cyclic C3-10 alkylene, an optionally substituted monocyclic or polycyclic aromatic heterocycle, a monocyclic or polycyclic aromatic ring or a partly saturated polycyclic aromatic ring; X represents O, CH2, C(=O) or NR11; and D is a group represented by the following general formula (4) or (6).-Q-Y-BIn the formula (6), Q represents a single bond, S, O or NR12; and Y is a group represented by the following general formula (7). z represents an optionally substituted monocyclic or polycyclic aromatic ring. In the formula (6), B represents NR25R26. In the above formulae, R1 to R26 each represents hydrogen, alkyl, alkenyl or alkynyl.

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