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16840-84-9

16840-84-9

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16840-84-9 Usage

General Description

10-Nonadecanol is a long-chain fatty alcohol that belongs to the class of organic compounds known as long-chain alcohols. It is a colorless solid with a waxy texture at room temperature and it is insoluble in water but soluble in organic solvents. 10-Nonadecanol is commonly used in the production of cosmetics, personal care products, and industrial applications, such as in the manufacturing of lubricants and plasticizers. It also exhibits antimicrobial properties and is used as an ingredient in some pharmaceutical and medicinal products. Additionally, it has been studied for its potential use in the synthesis of renewable biofuels.

Check Digit Verification of cas no

The CAS Registry Mumber 16840-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,4 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16840-84:
(7*1)+(6*6)+(5*8)+(4*4)+(3*0)+(2*8)+(1*4)=119
119 % 10 = 9
So 16840-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H40O/c1-3-5-7-9-11-13-15-17-19(20)18-16-14-12-10-8-6-4-2/h19-20H,3-18H2,1-2H3

16840-84-9SDS

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 nonadecan-10-ol

1.2 Other means of identification

Product number -
Other names 10-Nonadecanol

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:16840-84-9 SDS

16840-84-9Relevant articles and documents

COMPOUNDS USEFUL IN HIV THERAPY

-

Page/Page column 106-107; 135-136, (2021/10/02)

The invention relates to compounds of Formula (I), salts thereof, pharmaceutical compositions thereof, as well as methods of treating or preventing HIV in subjects.

TENSION SUPERFICIELLE ET MICELLISATION D'ALKYL SULFONATES DE SODIUM A DEUX CHAINES EGALES

Granet, Robert,Piekarski, Salomon

, p. 131 - 136 (2007/10/02)

Five new symetrical double tailed alkyl sodium sulfonates R(R)CH-SO3Na, each chain varying from 7 to 11 carbon atoms, have been synthesized and purified.Their solubilities in distillled water have been determined between 0 and 80 deg C.From measurement of surface tension, the curve γ = f(log C) permits the determination of the CMC and the surface excess.A linear plot of log(CMC) versus the total number of carbons have been established.The area per molecule near the CMC is the same for all the terms of the serie.The surface tension above the CMC decreases from 25.7 to 21.4 mN/m when the alkyl chain grows, from R = C7H16 to R = C11H23 at 60 deg C.In the presence of added NaCl, the area per molecule decreases to 55 +/- 5 Angstroem and the evolution of the CMC values versus salinity gives an estimation of the ionization degree of the micelles.

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