推荐产品
等级
reagent grade
蒸汽密度
4.63 (vs air)
蒸汽压
0.12 mmHg ( 20 °C)
产品线
Vetec™
检测方案
99%
形式
liquid
expl. lim.
1.2 %, 135 °F
23.5 %, 182 °F
杂质
≤0.10% water
water
折射率
n20/D 1.427 (lit.)
bp
202 °C (lit.)
mp
-80 °C (lit.)
密度
0.999 g/mL at 25 °C (lit.)
SMILES字符串
CCOCCOCCO
InChI
1S/C6H14O3/c1-2-8-5-6-9-4-3-7/h7H,2-6H2,1H3
InChI key
XXJWXESWEXIICW-UHFFFAOYSA-N
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法律信息
CARBITOL is a trademark of The Dow Chemical Company or an affiliated company of Dow
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
WGK
WGK 1
闪点(°F)
closed cup
闪点(°C)
closed cup
International journal of pharmaceutics, 423(2), 153-160 (2012-01-03)
To achieve rapid onset of action and improved bioavailability of udenafil, a microemulsion system was developed for its intranasal delivery. Phase behavior, particle size, transmission electron microscope (TEM) images, and the drug solubilization capacity of the microemulsion were investigated. A
Journal of drug targeting, 19(3), 189-196 (2010-05-08)
The aim of this work was to evaluate the ability of Transcutol (Trc) to produce elastic vesicles with soy lecithin (SL) and study the influence of the obtained vesicles on in vitro (trans)dermal delivery of minoxidil. To this purpose, so-called
Journal of cosmetic dermatology, 11(2), 101-110 (2012-06-08)
Skin-lightening preparations are used by people all over the world for a diverse range of dermatologic indications. The gold standard treatment for skin lightening is with hydroquinone but has been controversial because of the presence of several side effects. Therefore
International journal of pharmaceutics, 434(1-2), 264-271 (2012-05-31)
The objective of the present study was to enhance solubility and bioavailability of itraconazole by a combined use of membrane emulsification and spray drying solidification technique. A shirasu-porous-glass (SPG) membrane with a mean pore size of 2.5 μm was used
Regulatory toxicology and pharmacology : RTP, 57(2-3), 284-290 (2010-03-30)
Drug safety research is frequently faced with the challenge of the selection of appropriate vehicles for use in in vivo non-clinical safety assessment studies. Reported here are the results of blend Labrasol, Labrafil and Transcutol, [L/L/T, (4/4/2, v/v/v)], excipients used
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