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Key Documents

308153

Sigma-Aldrich

N-Propyl-1,3-propanediamine

99%

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About This Item

Linear Formula:
CH3CH2CH2NH(CH2)3NH2
CAS Number:
Molecular Weight:
116.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.4451 (lit.)

bp

169 °C (lit.)

density

0.841 g/mL at 25 °C (lit.)

SMILES string

CCCNCCCN

InChI

1S/C6H16N2/c1-2-5-8-6-3-4-7/h8H,2-7H2,1H3

InChI key

OWKYZAGJTTTXOK-UHFFFAOYSA-N

Related Categories

Application

N-Propyl-1,3-propanediamine was used in the synthesis of 1-benzotriazolylmethyl-3-propylhexahydropyrimidine.

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

129.2 °F - closed cup

Flash Point(C)

54 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Alan R Katritzky et al.
The Journal of organic chemistry, 67(9), 3115-3117 (2002-04-27)
1-Benzotriazolylmethyl-3-propylhexahydropyrimidine (1) and 1,3-bis(1H-1,2,3-benzotriazol-1-ylmethyl)-1,2,3,4-tetrahydroquinazoline (3) were readily prepared by reactions of N-propyl-1,3-propanediamine or 2-aminobenzylamine with benzotriazole and formaldehyde, respectively. Intermediate 1 reacted with alkyl and aryl Grignard reagents to produce N,N'-unsymmetrically substituted hexahydropyrimidines 2a,b in 90 and 92% yields, respectively.
Ahmed Salman et al.
Genes, 11(10) (2020-10-04)
In this study, we seek to exclude other pathophysiological mechanisms by which Frmd7 knock-down may cause Idiopathic Infantile Nystagmus (IIN) using the Frmd7.tm1a and Frmd7.tm1b murine models. We used a combination of genetic, histological and visual function techniques to characterize
C M Maragos et al.
Cancer research, 53(3), 564-568 (1993-02-01)
Cell-mediated antitumor effects have, in part, been attributed to the production of NO. Compounds which generate NO might, therefore, be useful in attenuating the growth of tumor cells. Six nitric oxide/nucleophile adducts that release NO spontaneously in solution were tested

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