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质量水平
表单
pellets
分子量
average Mn ~5,000
average Mw ~12,000
粘度
6.0 poise(190 °C, Brookfield Thermosel)(lit.)
mp
157 °C
酸值
<0.05 mg KOH/g
转变温度
softening point 163 °C (ring and ball, ASTM E 28)
密度
0.9 g/mL at 25 °C (lit.)
SMILES字符串
CC=C
InChI
1S/C22H42O3/c1-2-3-4-5-11-14-17-20-21(25-20)18-15-12-9-7-6-8-10-13-16-19-22(23)24/h20-21H,2-19H2,1H3,(H,23,24)/t20-,21+/m1/s1
InChI key
NSYDMBURIUSUDH-RTWAWAEBSA-N
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应用
用于减少结块、划痕和磨损的蜡改性剂。改善聚丙烯膜和纤维中颜料的分散性。
物理属性
低密度、低粘度的均聚物。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Hiroyuki Yanagisawa et al.
Molecules (Basel, Switzerland), 23(4) (2018-03-23)
This study was conducted with the aim of achieving the simultaneous screening of various additives in polymer materials by utilizing a solvent-free pyrolyzer/thermal desorption gas chromatography mass spectrometry (Py/TD-GC-MS) method. As a first step to achieve this goal, simultaneous screening
F Cassiola et al.
Artificial organs, 24(3), 168-173 (2000-04-12)
The introduction of microporous polypropylene hollow fibers in recent years has brought considerable advances to blood oxygenators. However, lifetime and assembly problems are still unresolved. In this work we tried to rate the oxygen permeation velocity by turning the fibers
[Procedure for membrane oxygenation of blood over hydrophilic polymer membranes].
H Körber et al.
Biomedizinische Technik. Biomedical engineering, 43 Suppl, 338-340 (1998-12-22)
G Imanidis et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 47(3), 283-287 (1999-06-26)
The possibility to control the release rate of salbutamol through the hydrophobic Celgard 2500 polypropylene membrane by varying the composition and the viscosity of hydrophilic drug vehicles was investigated. The use of the polypropylene membrane as a control membrane for
Simon J Gallagher et al.
Journal of drug targeting, 11(6), 373-379 (2003-12-12)
The aim of this study was to test the hypothesis that the most appropriate model for studying the diffusional release of an active from a topical formulation is one in which the membrane offers minimal resistance to release and involves
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