272264
1-(3-Aminopropyl)imidazole
≥97%
Sinónimos:
1-(3-Aminopropanyl)imidazole, 3-(1-Imidazolyl)propylamine, 3-(1H-Imidazol-1-yl)propylamine, 3-(Imidazol-1-yl)propylamine, N-(3-Aminopropyl)imidazole, N-[3-(1H-Imidazol-1-yl)propyl]amine
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Fórmula empírica (notación de Hill):
C6H11N3
Número CAS:
Peso molecular:
125.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
225-730-9
MDL number:
Assay:
≥97%
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥97%
form
liquid
refractive index
n20/D 1.519 (lit.)
density
1.049 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
NCCCn1ccnc1
InChI
1S/C6H11N3/c7-2-1-4-9-5-3-8-6-9/h3,5-6H,1-2,4,7H2
InChI key
KDHWOCLBMVSZPG-UHFFFAOYSA-N
Application
1-(3-Aminopropyl)imidazole was used in the synthesis of pH-sensitive polyaspartamide derivatives. It was also used in the preparation of pH-sensitive amphiphilic polymers with different degrees of octaceylamine (C18) substitution by graft reaction.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B
Clase de almacenamiento
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
309.2 °F
flash_point_c
154 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Kwangwon Seo et al.
Macromolecular bioscience, 6(9), 758-766 (2006-09-13)
New pH-sensitive polyaspartamide derivatives were synthesized by grafting 1-(3-aminopropyl)imidazole and/or O-(2-aminoethyl)-O'-methylpoly(ethylene glycol) 5000 on polysuccinimide for application in intracellular drug delivery systems. The DS of 1-(3-aminopropyl)imidazole was adjusted by the feed molar ratio, and the structure of the prepared polymer
Xiaodan Li et al.
Journal of controlled release : official journal of the Controlled Release Society, 260, 12-21 (2017-05-22)
Photodynamic therapy (PDT) efficacy is limited by the very short half-life and limited diffusion radius of singlet oxygen (
Kwangwon Seo et al.
Journal of nanoscience and nanotechnology, 10(10), 6986-6991 (2010-12-09)
The effect of hydrophobic octadecyl groups on pH-dependent aggregation behavior of polyaspartammide derivatives was studied. A series of pH-sensitive amphiphilic polymers with different degrees of octaceylamine (C18) substitution were synthesized through a successive graft reaction of octaceylamine, O-(2-aminoethyl)-O'-methylpolyethylene glycol, and