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1-Hexadecanol, 16-[(tetrahydro-2H-pyran-2-yl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139386-65-5

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139386-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139386-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,8 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139386-65:
(8*1)+(7*3)+(6*9)+(5*3)+(4*8)+(3*6)+(2*6)+(1*5)=165
165 % 10 = 5
So 139386-65-5 is a valid CAS Registry Number.

139386-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 16-(oxan-2-yloxy)hexadecan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Hexadecanol,16-[(tetrahydro-2H-pyran-2-yl)oxy]

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:139386-65-5 SDS

139386-65-5Upstream product

139386-65-5Relevant academic research and scientific papers

Scalable Synthesis of Human Ultralong Chain Ceramides

Opálka, Luká?,Ková?ik, Andrej,Sochorová, Michaela,Roh, Jaroslav,Kune?, Ji?í,Len?o, Juraj,Vávrová, Kate?ina

, p. 5456 - 5459 (2015/11/18)

Ceramides with ultralong chains (≥30 carbons), also known as acylceramides, play a critical role in the survival of mammals on dry land. An efficient and scalable synthesis of four major classes of ultralong human skin ceramides is reported. The key approach involves the use of a succinimidyl ester that acts as a protective group, helps overcome the extremely low solubility, and simultaneously activates the fatty acid for its clean and high-yielding attachment to a sphingoid base.

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