177504
十六烷二酸
96%
别名:
塔普酸
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关于此项目
线性分子式:
HOOC(CH2)14COOH
化学文摘社编号:
分子量:
286.41
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
208-013-5
Beilstein/REAXYS Number:
1792831
MDL number:
General description
十六烷二酸(HDDA)，又称它普酸，是直链的脂肪二羧酸，分子式C₁₆H30O₄。其饱和烃链的两端有两个羧酸基(-COOH)，赋予聚合物热稳定性、疏水性和生物相容性。
Application
十六烷二酸可用于：
- 作为心脏代谢成像的示踪剂（镓-68放射性标记），在心脏PET扫描中可视化脂肪酸代谢。它的生物相容性和天然脂肪酸途径模拟，可增强对心脏功能的诊断评估能力。
- 作为前体，经由熔融缩聚反应制备非交联三元共聚酯。所得材料可用于制作环保型食品包装材料。
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
A Aarsland et al.
Journal of lipid research, 30(11), 1711-1718 (1989-11-01)
Previous work in this laboratory indicated that sulfur-substituted fatty acid analogues, 1.10-bis(carboxymethylthio)decane and alkylthioacetic acid, both non-beta-oxidizable compounds, and the beta-oxidizable alkylthiopropionic acid (1) caused, to different extents, dose-related hepatomegaly and proliferation of peroxisomes and enhanced peroxisomal fatty acid beta-oxidation.
Young-Jae You et al.
European journal of medicinal chemistry, 39(2), 189-193 (2004-02-28)
Esters of 4'-demethyl-4-deoxypodophyllotoxin (DDPT) with alkanoic acids and alkanedioic acids were prepared and tested for cytotoxic and antitumor activity. Among 19 esters, esters of propanoic acid, tetradecanedioic acid, 13-carboxyundecanoic acid, and hexadecanedioic acid improved the antitumor activity compared with that
N Shirane et al.
Biochemistry, 32(49), 13732-13741 (1993-12-14)
Cytochrome P450BM-3 preferentially oxidized fatty acids with terminal double or triple bonds to the omega-2 hydroxylated fatty acids rather than, respectively, to the epoxide or diacid metabolites. The enzyme is inactivated during catalytic turnover of long, terminally unsaturated fatty acids
Anupam Mathur et al.
Bioorganic & medicinal chemistry, 16(17), 7927-7931 (2008-08-15)
Development of a (99m)Tc-fatty acid analogue is of interest, as (99m)Tc is logistically advantageous over the cyclotron-produced (11)C and (123)I. Synthesis of a 16 carbon fatty acid derivative and its radiolabeling with the novel [(99m)TcN(PNP)](2+) core is described here. Hexadecanedioic
J E Pettersen et al.
Journal of lipid research, 15(6), 551-556 (1974-11-01)
The activation of hexadecanedioic acid has been studied in subcellular fractions of human liver. The activation capacity in a total homogenate of human liver was found to be 0.5 micro mole/min/g wet wt of tissue, about 10% of that for
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