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2-BUTYL-1-DECANOL, also known as 2-butyldecyl alcohol, is a versatile chemical compound characterized by its colorless liquid form, mild pleasant odor, and solubility in ethanol and ether. It is insoluble in water and is recognized for its low volatility and high boiling point, making it a valuable additive in a variety of applications across the chemical and manufacturing industries.

21078-81-9

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21078-81-9 Usage

Uses

Used in Plastics Industry:
2-BUTYL-1-DECANOL is used as a plasticizer and lubricant for enhancing the flexibility and workability of plastics, particularly in the production of PVC. Its properties contribute to improved processing and performance of the final plastic products.
Used in Personal Care Products:
In the personal care industry, 2-BUTYL-1-DECANOL is used as an emollient and solvent in the formulation of various products such as creams, lotions, and cosmetics. Its mildness and solubility properties make it suitable for use in formulations that come into contact with the skin.
Used in Coatings and Adhesives:
2-BUTYL-1-DECANOL is utilized as a component in coatings and adhesives to improve their performance characteristics, such as adhesion, flexibility, and durability. Its role as a solvent helps in the proper dispersion of other ingredients, ensuring a uniform and effective end product.
Used in Industrial Processes:
As a solvent, 2-BUTYL-1-DECANOL is employed in various industrial processes to dissolve and carry other substances, facilitating chemical reactions and material treatments. Its high boiling point and low volatility are advantageous in applications requiring controlled evaporation rates.
Used as an Intermediate in Chemical Production:
2-BUTYL-1-DECANOL also serves as an intermediate in the synthesis of other chemicals, expanding its utility in the chemical manufacturing sector. Its ability to undergo further reactions makes it a key component in creating a range of derivative products.

Check Digit Verification of cas no

The CAS Registry Mumber 21078-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,7 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21078-81:
(7*2)+(6*1)+(5*0)+(4*7)+(3*8)+(2*8)+(1*1)=89
89 % 10 = 9
So 21078-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H30O/c1-3-5-7-8-9-10-12-14(13-15)11-6-4-2/h14-15H,3-13H2,1-2H3

21078-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyldecan-1-ol

1.2 Other means of identification

Product number -
Other names 2-butyloctanol

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:21078-81-9 SDS

21078-81-9Downstream Products

21078-81-9Relevant academic research and scientific papers

GUERBET CONDENSATION REACTION

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Page/Page column 17-18; 30-31, (2017/07/08)

The invention relates to a process for the preparation of a Guerbet alcohol, comprising the steps of: (a) providing at least one alcohol, wherein said at least one alcohol has a carbon atom bearing at least one hydrogen atom adjacent to the hydroxyl group; (b) providing a catalyst composition, wherein said catalyst composition comprises an alkaline catalyst and a copper-nickel catalyst comprised in a hydrotalcite; (c) mixing alcohol (a) with catalyst composition (b), thereby obtaining a mixture; and, (d) heating said mixture; thereby obtaining a Guerbet alcohol.

Amides for the treatment of atherosclerosis

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, (2008/06/13)

This invention provides amide compounds as inhibitors of acyl-Coenzyme A: cholesterol O-acyltransferase (ACAT), pharmaceutical compositions containing such compounds, processes for the preparation of such compounds, and the use of such compounds as antihypercholesterolemic and/or antiatherosclerotic agents.

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