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1184-05-0

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  • [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] octadecanoate

    Cas No: 1184-05-0

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1184-05-0 Usage

General Description

Cholesteryl stearate is a chemical compound that consists of a cholesterol molecule bonded to a stearic acid molecule. It is a waxy, odorless solid that is insoluble in water and stable at room temperature. Cholesteryl stearate is commonly used in the cosmetic and personal care industry as an additive in skincare and hair care products due to its emollient properties, which help to soften and smooth the skin and hair. It also functions as a thickening agent in various cosmetic formulations, providing a smooth and creamy texture. Additionally, cholesteryl stearate is used in the pharmaceutical industry as an excipient in the manufacture of oral and topical medications.

Check Digit Verification of cas no

The CAS Registry Mumber 1184-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1184-05:
(6*1)+(5*1)+(4*8)+(3*4)+(2*0)+(1*5)=60
60 % 10 = 0
So 1184-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C45H80O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25-43(46)47-38-30-32-44(5)37(34-38)26-27-39-41-29-28-40(36(4)24-22-23-35(2)3)45(41,6)33-31-42(39)44/h26,35-36,38-42H,7-25,27-34H2,1-6H3/t36-,38+,39+,40?,41+,42+,44+,45-/m1/s1

1184-05-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] octadecanoate

1.2 Other means of identification

Product number -
Other names 2,15-dimethyl-14-(6-methylheptan-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl octadecanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1184-05-0 SDS

1184-05-0Downstream Products

1184-05-0Relevant articles and documents

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Labarrere et al.

, p. 1466,1468 (1958)

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Purification of recombinant acyl-coenzyme a:cholesterol acyltransferase 1 (ACAT1) from H293 cells and binding studies between the enzyme and substrates using difference intrinsic fluorescence spectroscopy

Chang, Catherine C. Y.,Miyazaki, Akira,Dong, Ruhong,Kheirollah, Alireza,Yu, Chunjiang,Geng, Yong,Higgs, Henry N.,Chang, Ta-Yuan

, p. 9957 - 9963 (2010)

Acyl-coenzyme A:cholesterol acyltransferase 1 (ACAT1) is a membrane-bound enzyme utilizing long-chain fatty acyl-coenzyme A and cholesterol to form cholesteryl esters and coenzyme A. Previously, we had expressed tagged human ACAT1 (hACAT1) in CHO cells and purified it to homogeneity; however, only a sparse amount of purified protein could be obtained. Here we report that the hACAT1 expression level in H293 cells is 18-fold higher than that in CHO cells. We have developed a milder purification procedure to purify the enzyme to homogeneity. The abundance of the purified protein enabled us to conduct difference intrinsic fluorescence spectroscopy to study the binding between the enzyme and its substrates in CHAPS/phospholipid mixed micelles. The results show that oleoyl-CoA binds to ACAT1 with Kd = 1.9 μM and elicits significant structural changes of the protein as manifested by the significantly positive changes in its fluorescence spectrum; stearoyl-CoA elicits a similar spectrum change but much lower in magnitude. Previously, kinetic studies had shown that cholesterol is an efficient substrate and an allosteric activator of ACAT1, while its diastereomer epicholesterol is neither a substrate nor an activator. Here we show that both cholesterol and epicholesterol induce positive changes in the ACAT1 fluorescence spectrum; however, the magnitude of spectrum changes induced by cholesterol is much larger than epicholesterol. These results show that stereospecificity, governed by the 3β-OH moiety in steroid ring A, plays an important role in the binding of cholesterol to ACAT1.

COMPOSITION FOR PREVENTING HAIR LOSS AND ACCELERATING HAIR GROWTH

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Paragraph 0017, (2015/10/05)

Disclosed is a composition for prevention of hair loss and promotion of hair growth. The composition includes a compound represented by Formula 1, wherein A is derived from polycyclic compounds, and R is a hydroxyl group, or a saturated or unsaturated straight or branched alkyloxy or acyloxy group having 1 to 20 carbon atoms.

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