308153

Sigma-Aldrich

N-Propyl-1,3-propanediamine

99%

Linear Formula:
CH3CH2CH2NH(CH2)3NH2
CAS Number:
Molecular Weight:
116.20
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

assay

99%

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

Application

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

Packaging

5 g in glass bottle

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 2734PSN2 3(8) / PGII

WGK Germany

WGK 3

Flash Point(F)

129.2 °F - closed cup

Flash Point(C)

54 °C - closed cup

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....
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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