272264
1-(3-Aminopropyl)imidazole
≥97%
Synonyme(s) :
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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A propos de cet article
Formule empirique (notation de Hill) :
C6H11N3
Numéro CAS:
Poids moléculaire :
125.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
225-730-9
MDL number:
Assay:
≥97%
Form:
liquid
Service technique
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Laissez-nous vous aiderQuality 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
Classe de stockage
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.
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
Taehoon Sim et al.
Pharmaceutics, 12(9) (2020-09-06)
Combination therapy is considered to be a promising strategy for improving the therapeutic efficiency of cancer treatment. In this study, an on-demand pH-sensitive nanocluster (NC) system was prepared by the encapsulation of gold nanorods (AuNR) and doxorubicin (DOX) by a
Abootaleb Sedighi et al.
Talanta, 186, 568-575 (2018-05-23)
Several solution-based methods have recently been adapted for use in paper substrates for enzymatic amplification to increase the number of copies of DNA sequences. There is limited information available about the impact of a paper matrix on DNA amplification by