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2-Ethyltridecanoic acid, also known as 2-ethyl-2-tridecanoic acid, is a chemical compound with the molecular formula C16H32O2. It is a saturated fatty acid with a 16-carbon backbone and a carboxylic acid group. 2-Ethyltridecanoic acid is characterized by its solubility in organic solvents and a distinctive fatty odor.

69868-07-1

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69868-07-1 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Ethyltridecanoic acid is used as a building block in the synthesis of pharmaceuticals for its unique structural properties that can be incorporated into drug molecules to enhance their efficacy and pharmacokinetics.
Used in Surfactant Production:
In the chemical industry, 2-Ethyltridecanoic acid serves as a key component in the production of surfactants, which are essential for creating stable emulsions and dispersions in various applications, including detergents, cosmetics, and industrial processes.
Used in the Production of Lubricants:
2-Ethyltridecanoic acid is utilized as a raw material in the formulation of lubricants due to its ability to reduce friction and wear between moving parts, thus extending the life of machinery and equipment.
Used in Emulsifier Formulation:
2-Ethyltridecanoic acid is used as an emulsifier, which helps in mixing immiscible liquids such as oil and water, and is crucial in the food, cosmetic, and pharmaceutical industries for creating stable mixtures and improving product performance.
Used in Corrosion Inhibitor Formulation:
2-Ethyltridecanoic acid is used as a corrosion inhibitor, protecting metals from degradation and rusting, which is particularly important in industries such as automotive, aerospace, and construction where metal protection is critical.
Used in Natural Oils and Fats:
It is also found in some natural oils and fats, contributing to their properties and uses in various applications, including food products and personal care items.
Given its low toxicity and general safety, 2-Ethyltridecanoic acid is a versatile compound suitable for a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 69868-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69868-07:
(7*6)+(6*9)+(5*8)+(4*6)+(3*8)+(2*0)+(1*7)=191
191 % 10 = 1
So 69868-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O2/c1-3-5-6-7-8-9-10-11-12-13-14(4-2)15(16)17/h14H,3-13H2,1-2H3,(H,16,17)

69868-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyltridecanoic acid

1.2 Other means of identification

Product number -
Other names EINECS 274-169-6

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:69868-07-1 SDS

69868-07-1Upstream product

69868-07-1Downstream Products

69868-07-1Relevant academic research and scientific papers

SELECTIVE MIXED COUPLING OF CARBOXYLIC ACIDS (II). -PHOTOLYSIS OF UNSYMMETRICAL DIACYLPEROXIDES WITH ALKENYL-, HALO-, KETO-, CARBOXYL-GROUPS AND A CHIRAL α-CARBON. COMPARISON WITH THE MIXED KOLBE ELECTROLYSIS.

Feldhues, Michael,Schaefer, Hans J.

, p. 4213 - 4236 (2007/10/02)

- Alkenoyl and functionalized alkanoyl dodecanoyl peroxides are prepared in 70 to 97 percent yield and photolyzed at -78 deg C.Thereby 4- to 10-alkenoyl and 4-alkynoyl peroxides afford good yields (56 - 68 percent) of unsymmetrical coupling products.Similarly α- to δ-haloalkanoyl, cholanoyl or 3- and 4-carboxyalkanoyl peroxides can be coupled (40 - 70 percent).The α-chiral diacyl peroxide 1s undergoes the photochemical coupling reaction with 80 percent retention of its configuration.The photolysis of diacyl peroxides at -78 deg C proves to be a favorable supplement of the Kolbe-electrolysis in cases, where the electrolysis fails or produces low yields.

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