D16401
1,12-十二烷二元胺
98%
别名:
1,12-十二烷胺, 十二亚甲基二胺
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关于此项目
线性分子式:
NH2(CH2)12NH2
化学文摘社编号:
分子量:
200.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-489-6
Beilstein/REAXYS Number:
1742765
MDL number:
产品名称
1,12-十二烷二元胺, 98%
InChI key
QFTYSVGGYOXFRQ-UHFFFAOYSA-N
InChI
1S/C12H28N2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-14H2
SMILES string
NCCCCCCCCCCCCN
assay
98%
form
flakes
mp
67-69 °C (lit.)
Quality Level
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Application
用于聚合物合成的原料。用于药物的十二碳链源。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
311.0 °F - closed cup
flash_point_c
155 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Michelle Henderson Pozzi et al.
Biochemistry, 48(7), 1508-1516 (2009-02-10)
Mammalian polyamine oxidases (PAOs) catalyze the oxidation of N1-acetylspermine and N1-acetylspermidine to produce N-acetyl-3-aminopropanaldehyde and spermidine or putrescine. Structurally, PAO is a member of the monoamine oxidase family of flavoproteins. The effects of pH on the kinetic parameters of mouse
Kangkyun Baek et al.
Chemical communications (Cambridge, England), 46(23), 4091-4093 (2010-05-19)
The X-ray crystal structure of 1,12-dodecane diammonium (C(12)DA(2+)) encapsulated in cucurbit[8]uril reveals an unconventional U-shaped conformation of C(12)DA(2+), which is attributed to the favorable host-guest interactions to overcome the charge-charge repulsion of the two ammonium groups in close proximity and
E Dziembor-Gryszkiewicz et al.
Biochemistry international, 6(5), 627-633 (1983-05-01)
The acid phosphatase [EC 3.1.3.2] from human prostate gland is very unstable glycoprotein. To stabilize the enzyme cross-linking reaction with diamines was adopted. The carboxyl groups of the enzyme were activated with 1-ethyl-(3-dimethylaminopropyl)-carbodiimide and then treated with diamines of H2N-(CH2)n-NH2
T M Weiger et al.
Biophysical journal, 74(2 Pt 1), 722-730 (1998-04-09)
In this study we compared polyamines to various diamines, and we modeled flexibility as well as hydrophobicity properties of these molecules to examine possible structural differences that could explain their external effects on the channels. The natural polyamines (putrescine, cadaverine
Andrew R Hirst et al.
Langmuir : the ACS journal of surfaces and colloids, 20(25), 10851-10857 (2004-12-01)
The self-assembly of diaminododecane with dendritic l-lysine-based peptides to form gel-phase materials was investigated in a range of different solvents. The degree of structuring was modulated by the solvent employed, an effect which induced subtle changes in the mesoscale aggregate
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