85730
硬酯酰氯
technical, ≥90% (GC), strongly brown
别名:
十八烷酰氯
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关于此项目
线性分子式:
CH3(CH2)16COCl
化学文摘社编号:
分子量:
302.92
Beilstein:
639784
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
等级
technical
质量水平
方案
≥90% (GC)
表单
liquid
颜色
strongly brown
折射率
n20/D 1.454 (lit.)
沸点
174-178 °C/2 mmHg (lit.)
mp
21-22 °C (lit.)
密度
0.897 g/mL at 25 °C (lit.)
官能团
acyl chloride
SMILES字符串
CCCCCCCCCCCCCCCCCC(Cl)=O
InChI
1S/C18H35ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3
InChI key
WTBAHSZERDXKKZ-UHFFFAOYSA-N
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应用
Stearoyl chloride can modify cellulose diacetate (CDA) by replacing residual free hydroxyl groups in synthesizing materials that are used to produce surgical masks, smocks and other industrial products to absorb dust and haze-fog. It can be used in the synthesis of ultrastable coaxial cable-like superhydrophobic mesh. It is also used in the synthesis of stearoyl modified chitosan as drug vehicles for paclitaxel delivery.
警示用语：
Danger
危险声明
危险分类
Skin Corr. 1B
补充剂危害
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 2
闪点(°F)
329.0 °F - closed cup
闪点(°C)
165 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
Ultrastable coaxial cable-like superhydrophobic mesh with self-adaption effect: facile synthesis and oil/water separation application.
Xiao C, et al.
Journal of Material Chemistry A, 4(21), 8080-8090 (2016)
Acylation of Cellulose Diacetate by Stearoyl Chloride and Characterization for the Acylated Product.
Wang Q, et al.
J. Polym. Mater., 32(4) (2015)
Amphiphilic nanoparticles based on poly (vinyl pyrrolidone) and stearoyl modified chitosan as drug vehicles for paclitaxel delivery.
Liu Z, et al.
Materials Letters, 185, 226-229 (2016)
Çağla Koşak Söz et al.
ACS applied materials & interfaces, 10(43), 37478-37488 (2018-10-27)
We introduce the design of Janus-type paper sheets where one side of the paper exhibits superhydrophobic properties, whereas the other side of the sheet remains hydrophilic and therefore can take up aqueous solutions by capillary wicking. Such papers are being
A V Kabanov et al.
Biomedical science, 1(1), 63-67 (1990-01-01)
A method is proposed for the inhibition of viral reproduction in cells by means of fatty-acylated antiviral antibodies which, in contrast to the unmodified antibodies, have the ability to enter the cells. The potential of this technique is demonstrated in
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