推荐产品
等级
certified reference material
Agency
ERM®
制造商/商品名称
JRC
密度
0.9 g/mL at 25 °C (lit.)
应用
chemicals and industrial polymers
包装形式
neat
储存温度
−20°C
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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分析说明
For more information please see:
ERMEC591
ERMEC591
法律信息
ERM is a registered trademark of European Commission
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Thomas P J Linsinger et al.
Analytical chemistry, 81(10), 3792-3800 (2009-03-28)
The first reference materials certified for several polybrominated flame retardants in polymers were developed. Commercially available polyethylene and polypropylene were fortified with technical mixtures of Pentabrominated diphenylether (Penta-BDE), Octa-BDE, Deca-BDE, and Decabrominated biphenyl (BB) (where the capitalized forms refer to
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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