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Octadecane-1,9,10-triol, also known as 1,9,10-trihydroxyoctadecan-2-one or glycerol tristearate, is a naturally occurring organic compound with the chemical formula C39H76O5. It is a triglyceride, which is a type of ester derived from glycerol and three fatty acids, specifically stearic acid in this case. Octadecane-1,9,10-triol is a waxy, white solid that is insoluble in water but soluble in organic solvents. It is commonly found in various plant and animal fats, and is used in the food industry as an emulsifier, stabilizer, and texturizer. Additionally, it has applications in the cosmetics and pharmaceutical industries due to its moisturizing and skin conditioning properties.

7023-01-0

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7023-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7023-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7023-01:
(6*7)+(5*0)+(4*2)+(3*3)+(2*0)+(1*1)=60
60 % 10 = 0
So 7023-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H38O3/c1-2-3-4-5-8-11-14-17(20)18(21)15-12-9-6-7-10-13-16-19/h17-21H,2-16H2,1H3

7023-01-0SDS

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 (9SR,10SR)-octadecane-1,9,10-triol

1.2 Other means of identification

Product number -
Other names 1,9,10-OCTADECANETRIOL

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:7023-01-0 SDS

7023-01-0Relevant academic research and scientific papers

Hot water as a mild Bronsted acid catalyst in ring opening reactions of epoxides

Xu, Zhaobing,Qu, Jin

experimental part, p. 1718 - 1725 (2012/04/18)

Ring opening of extremely hydrophobic epoxides with water, amines, sodium azide and thiophenol was realized in the mixture solvent of water and 1, 4-dioxane under reflux condition. Hot water was believed to act as a mild Bronsted acid catalyst in the epoxide-opening reactions.

Modified isocyanates

-

, (2009/12/27)

Modified stable polyisocyanates are described having at least one isocyanate function modified by a group having cross-linking functionality. The modified stable polyisocyanates may be prepared by reacting at least one polyisocyanate with a compound of the formula:

Synthesis and Characterization of Single-Chain Second Generation Cleavable Surfactants

Jaeger, David A.,Sayed, Yasmin M.

, p. 2619 - 2627 (2007/10/02)

Three series of single-chain, second generation cleavable surfactants, trans-trimethylammonium methanesulfonate (1) and sodium (2) and triethanolammonium trans-8-(2,2-dialkyl-5-octyl-1,3-dioxolan-4-yl)octane-1-sulfate (3) (a, R = Me; b, R = Et; c, R = Pr; d, R = Bu), were prepared.They were characterized by critical micelle concentration, Krafft temperature, and dynamic laser light scattering measurements.Acid-catalyzed hydrolysis of surfactants 1, 2, and 3 gives (threo-9,10-dihydroxyoctadecyl)trimethylammonium methanesulfonate (4) and sodium (6) and triethanolammonium threo-9,10-dihydroxyoctadecane-1-sulfate (7), respectively, and a dialkyl ketone 5 (a, Me2CO; b, Et2CO; c, Pr2CO; d, Bu2CO).Cleavage of these surfactants thus gives another surfactant, with a higher critical micelle concentration, and a water-soluble neutral compound.Surfactants 3 were about 20 times more reactive than 1.

Non-metal-requiring Catalyst Contained in Recovered Methyl Linolenate from an Autoxidizing Sample

Morita, Makio

, p. 2403 - 2408 (2007/10/02)

Non-metal-requiring catalysts in recovered methyl lenolenate from an autoxidizing sample were unstable on contact with silicic acid and the activity varied widely with the way of recovery, countercurrent extraction and column chromatography under different conditions.After reduction with stannous chloride, a substance was found which was characteristically present in the products deriver from the recovered methyl linolenate high in the catalytic activity.It was tentatively indentified by MS, IR, OsO4 oxidation-IO41- oxidation, and LiAlH4 reduction-IO41- oxidation as methyl 9,13-dihydroxy-10-epoxy-15-octadecenoate.

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