308153
N-Propyl-1,3-propanediamine
99%
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About This Item
Linear Formula:
CH3CH2CH2NH(CH2)3NH2
CAS Number:
Molecular Weight:
116.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
245-869-9
MDL number:
Product Name
N-Propyl-1,3-propanediamine, 99%
InChI key
OWKYZAGJTTTXOK-UHFFFAOYSA-N
InChI
1S/C6H16N2/c1-2-5-8-6-3-4-7/h8H,2-7H2,1H3
SMILES string
CCCNCCCN
assay
99%
form
liquid
refractive index
n20/D 1.4451 (lit.)
bp
169 °C (lit.)
density
0.841 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
Related Categories
Application
N-Propyl-1,3-propanediamine was used in the synthesis of 1-benzotriazolylmethyl-3-propylhexahydropyrimidine.
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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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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