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1-Octadecanol methyl ether, also known as methyl octadecyl ether or methylstearyl ether, is a chemical compound with the molecular formula C19H38O. It is a colorless to pale yellow liquid with a mild, characteristic odor. This ether derivative is derived from 1-octadecanol, a long-chain alcohol, and is formed by the reaction of 1-octadecanol with methyl iodide or other methylating agents. 1-Octadecanol methyl ether is used in various applications, including as a non-ionic surfactant, emulsifier, and intermediate in the synthesis of other chemicals. It is also found in some personal care products and pharmaceuticals due to its solubilizing and stabilizing properties.

6838-81-9

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6838-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6838-81-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6838-81:
(6*6)+(5*8)+(4*3)+(3*8)+(2*8)+(1*1)=129
129 % 10 = 9
So 6838-81-9 is a valid CAS Registry Number.

6838-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-octadecane

1.2 Other means of identification

Product number -
Other names 1-Methoxy-octadecan

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:6838-81-9 SDS

6838-81-9Upstream product

6838-81-9Downstream Products

6838-81-9Relevant academic research and scientific papers

A triruthenium carbonyl cluster bearing a bridging acenaphthylene ligand: An efficient catalyst for reduction of esters, carboxylic acids, and amides by trialkylsilanes

Matsubara, Kouki,Iura, Takafumi,Maki, Tomoyuki,Nagashima, Hideo

, p. 4985 - 4988 (2007/10/03)

An efficient reduction of carboxylic acids, esters, and amides with trialkylsilanes is accomplished using a triruthenium carbonyl cluster bearing a bridging acenaphthylene ligand, (μ3,η2:η3:η5 -acenaphthylene)Ru3(CO)7, as the catalyst. Preactivation of the catalyst by hydrosilanes accelerates the reactions. Sterically small trialkylsilanes are effective in these reactions. Reduction of carboxylic acids and amides efficiently produces the corresponding silyl ethers and amines, respectively. Reduction of esters gives a mixture of silyl and alkyl ethers, but can be controlled by changing the silanes and solvents.

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