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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线性分子式:
NH2(CH2)12NH2
化学文摘社编号:
分子量:
200.36
Beilstein:
1742765
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
98%
表单
flakes
mp
67-69 °C (lit.)
SMILES字符串
NCCCCCCCCCCCCN
InChI
1S/C12H28N2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-14H2
InChI key
QFTYSVGGYOXFRQ-UHFFFAOYSA-N
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应用
用于聚合物合成的原料。用于药物的十二碳链源。
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
311.0 °F - closed cup
闪点(°C)
155 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
R Hochreiter et al.
Naunyn-Schmiedeberg's archives of pharmacology, 361(3), 235-246 (2000-03-24)
A series of diamines with the general structure NH2(CH2)xNH2, x=2-12, was tested for their potential effects on cell proliferation of cultured rat C6 glioma cells in comparison to natural polyamines. Long chain diamines reduced cell number after 48 h in
J Lee et al.
Journal of nanoscience and nanotechnology, 1(1), 59-64 (2003-08-14)
The partial exchange of surface-passivating trioctylphosphine oxide (TOPO) on CdSe and ZnS-clad CdSe (CdSe/ZnS) nanocrystals with primary amines was utilized to grow ultra-thin films of these nanocrystals under nonaqueous conditions. This growth was achieved using 1,12-diaminododecane in a layer-by-layer assembly
Michelle J Pisani et al.
Dalton transactions (Cambridge, England : 2003), 39(8), 2078-2086 (2010-02-12)
A simpler method for the purification of cucurbit[10]uril (Q[10]) from the Q[10].Q[5] inclusion complex is reported. 1,12-Diaminododecane was used to displace Q[5], as opposed to the synthetic melamine derivative currently used. The binding of trans-[{PtCl(NH(3))(2)}(2)(micro-NH(2)(CH(2))(8)NH(2))](2+) (CT008) and [{Ru(phen)(2)}(2)(micro-bb(5))](4+) {phen =
A Sintov et al.
Biomaterials, 16(6), 473-478 (1995-04-01)
Chondroitin sulphate was cross-linked with 1,12-diaminododecane to give a series of cross-linked products with reduced water solubility. Since the water solubility of the modified polymers is low, their chemical characterization is complicated. A new method based on the adsorption of
Beibei Xue et al.
Journal of integrative plant biology, 51(3), 225-234 (2009-03-06)
Using pharmacological and biochemical approaches, the role of maize polyamine oxidase (MPAO) in abscisic acid (ABA)-induced antioxidant defense in leaves of maize (Zea mays L.) plants was investigated. Exogenous ABA treatment enhanced the expression of the MPAO gene and the
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