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Detail of "1062-96-0"

  • CAS Number:
  • 1062-96-0
  • Name:
  • Cholest-5-en-3-ol (3b)-, hexanoate

  • Superlist Name:
  • Cholesteryl hexanoate
  • Molecular Structure:
  • Formula:
  • C33H56O2
  • Molecular Weight:
  • 484.80
  • Deleted CAS:
  • 313219-53-3
  • Synonyms:
  • Cholesterol,hexanoate (6CI,7CI,8CI);Hexanoic acid, cholesteryl ester (8CI);3b-(Caproyloxy)cholest-5-ene;5-Cholesten-3b-olcaproate;Cholest-5-en-3b-ol caproate;Cholesterol caproate;Cholesteryl caproate;
  • EINECS:
  • 213-899-1
  • Density:
  • 0.982 g/cm3
  • Melting Point:
  • 96 °C
  • Boiling Point:
  • 541.842 °C at 760 mmHg
  • Flash Point:
  • 279.217 °C

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CAS No.1062-96-0 Cholesteryl hexanoate

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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ISO 3875Integral
3875

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Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.1062-96-0 Cholesteryl hexanoate

CHOLESTERYL CAPROATE (HEXANOATE) CAS 1062-96-0 made on a custom basis

Supplier:Pressure Chemical Co. [ United States]

740Integral
740

Tel:412-682-5882

Address:3419 Smallman Street

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CAS No.1062-96-0 Cholesteryl hexanoate

Cholesteryl hexanoate

Supplier:TRUST&WE CO.,Ltd. [ China (Mainland)]

620Integral
620

Tel:+86-021-61551611

Address:No. 317, 219 Nong, Gao Muqiao Road, Zhangjiang Hightech. Park, Pudong, Shanghai

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CAS No.1062-96-0 Cholesteryl hexanoate

C33H56O2 99%

Supplier:Changzhou Vx Chemical Co.,Ltd [ China (Mainland)]

610Integral
610

Tel:+86-519-86011997

Address:NO.5 Binjiang Road, Jiangbian Chemical Park, Xinbei District

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Reference

Accumulation-type liquid crystal electrooptical display devices
Accumulation-type liquid crystal electrooptical display devices. Watanuki, Tsuneo; Iwasaki, Masayuki; Mochizuki, Akihiro; Saito, Kazumasa; Ikegami, Yoshizumi (Fujitsu Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 61197681 A2 1 Sep 1986 Showa, 6 pp. 604-35-3 and 1062-96-0 are also occured in this study. (Japan) CODEN: JKXXAF. CLASS: ICM: C09K019-50. ICS: C09K019-36; G02F001-13; G02F001-137. APPLICATION: JP 85-36297 27 Feb 1985. DOCUMENT TYPE: Patent CA Section: 74 (Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes) The liq. crystal compn. of the device contains 10-30% of a cholesteric liq. crystal compd. of the formula I (n = 0, 4) (e.g., cholesteryl acetate) that displays a pos. dielec. anisotropy. The display shows 2 optical states, i.e., a focal conic opaque state and a homeotropic transparent state, by applying an elec. potential to change the liq. crystal compn. between the cholesteric phase and nematic phase. The device provides a display with improved stability; it can provide large capacity displays and respond to keyboard input. .
Effect of cholesterol and cholesterol esters on the permeability and physical state of membranes
Effect of cholesterol and cholesterol esters on the permeability and physical state of membranes. Vasserman, A. N. (USSR). Deposited Doc. 1062-96-0 and 604-35-3 are also occured in this study., VINITI 5150-82, 229-37 Avail. VINITI (Russian) 1982. DOCUMENT TYPE: Report CA Section: 6 (General Biochemistry) Section cross-reference(s): 14 The introduction of cholesterol into planar bilayer lipid membranes (BLM) of pure lecithin decreased the membrane cond. ~50-fold from its initial level of 5.6 ′ 10-8 W-1 cm-2, presumably due to its ability to decrease the mobility of the hydrocarbon side chains. The cond. of thiophosphatidic acid BLM was less influenced by cholesterol than was that of lecithin membranes, probably reflecting differences in the mobilities of their hydrocarbon side chains. Addn. of cholesterol esters increased the membrane cond. of both lecithin and thiophosphatidic acid BLM, irresp. of the type of ester bond, in contrast to the effect of cholesterol. Even large amts. of cholesterol did not reverse the effect of the esters. The incorporation of even small amts. of cholesterol esters into the plasma membranes of vessel intimae may increase their permeability to ions and other metabolites, which could in turn disturb the cellular ionic balance and result in cell death. The possible relation of these results with the mechanism of atherosclerosis is discussed. .
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