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26533-36-8

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26533-36-8 Usage

Description

2-Nonadecanol, also known as eicosanol, is a long-chain fatty alcohol with a molecular formula of C20H42O. It is a waxy solid at room temperature and is commonly found in plant waxes and animal fats. 2-Nonadecanol is known for its variety of industrial applications and its relatively safe profile for human and environmental health, characterized by low toxicity and minimal risk of adverse effects.

Uses

Used in Lubricant Industry:
2-Nonadecanol is used as a lubricant due to its waxy solid nature at room temperature, providing a smooth and effective means of reducing friction between surfaces.
Used as an Emulsifier:
In the emulsification process, 2-Nonadecanol serves as an emulsifier, helping to mix and stabilize oil and water, which are typically immiscible.
Used in Cosmetics and Pharmaceuticals:
2-Nonadecanol is utilized in the production of cosmetics and pharmaceuticals, where its properties contribute to the formulation of various products, enhancing their texture, stability, and efficacy.
Used as a Raw Material for Chemical Synthesis:
2-Nonadecanol is also used as a raw material for the synthesis of other chemicals, such as surfactants and detergents, where its long-chain structure plays a crucial role in the performance of these products.
Used in Antimicrobial Applications:
2-Nonadecanol exhibits antimicrobial properties, making it a potential candidate for use in applications requiring the control of microbial growth.
Used as an Insecticide and Insect Repellent:
Due to its potential as an insecticide and insect repellent, 2-Nonadecanol can be employed in agricultural and household settings to manage and deter insect populations.

Check Digit Verification of cas no

The CAS Registry Mumber 26533-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26533-36:
(7*2)+(6*6)+(5*5)+(4*3)+(3*3)+(2*3)+(1*6)=108
108 % 10 = 8
So 26533-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H40O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(2)20/h19-20H,3-18H2,1-2H3

26533-36-8SDS

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 nonadecan-2-ol

1.2 Other means of identification

Product number -
Other names 2-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:26533-36-8 SDS

26533-36-8Downstream Products

26533-36-8Relevant articles and documents

Design of Manganese Phenol Pi-complexes as Shvo-type Catalysts for Transfer Hydrogenation of Ketones

Shvydkiy, Nikita V.,Vyhivskyi, Oleksandr,Nelyubina, Yulia V.,Perekalin, Dmitry S.

, p. 1602 - 1605 (2019/03/07)

Catalytic hydrogenation is one of the most important reactions both in academic research and industry. We explored ability of the manganese pi-complexes to act as Shvo-type catalysts for transfer hydrogenation of ketones. DFT calculations suggested that the transfer of hydrogen atoms from the hypothetical intermediate [(C6Me3H2OH)Mn(CO)2H] to acetone has low activation barrier of 10.9 kcal mol?1. Experimentally a number of ketones with various functional groups (OMe, NH2, Cl, CF3, pyridyl) were successfully reduced in isopropanol at 90 °C in the presence of the complex [(C6Me3H2OH)Mn(CO)3]BF4 (1 mol %) and tBuOK (75 mol %). However, further investigation revealed that the reduction was mainly promoted by base rather than the manganese complex.

Studies on PPL catalyzed acetylation of 2-alkanols: Its application for the synthesis of 2-dodecanol and 2-tridecyl acetate, the pheromones of Crematogaster ants and Drosophila mulleri flies

Sharma, Anubha,Pawar, Archana S.,Chattopadhyay, Subrata

, p. 19 - 25 (2007/10/03)

Several aliphatic 2-alkanols with varying chain length has been efficiently resolved by their acetylation using vinyl acetate/PPL in diisopropyl ether. The effect of solvent polarity, position and type of unsaturation and chain length has been probed. This has led to more convenient synthesis of some insect pheromones.

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