27610-92-0 Usage
Description
2-Butyloctanoic acid, a 2-butyl-substituted carboxylic acid, is a colorless liquid with unique chemical properties that make it suitable for various applications across different industries.
Uses
Used in Environmental Applications:
2-Butyloctanoic acid is used as a catalyst in the Fenton and photo-Fenton oxidation processes for the treatment of textile effluents. Its application in this context is due to its ability to enhance the degradation of pollutants and improve the overall efficiency of the wastewater treatment process.
Used in Chemical Industry:
2-Butyloctanoic acid serves as an important intermediate in the synthesis of various chemicals, pharmaceuticals, and specialty products. Its unique structure allows for the creation of a wide range of derivatives, making it a versatile building block in the chemical industry.
Used in Pharmaceutical Applications:
Due to its chemical properties, 2-butyloctanoic acid can be used as a starting material for the development of new drugs or as a component in the formulation of existing medications. Its versatility in chemical reactions enables the creation of novel compounds with potential therapeutic applications.
Used in Cosmetics and Personal Care:
The unique properties of 2-butyloctanoic acid make it a valuable ingredient in the cosmetics and personal care industry. It can be used as a component in the formulation of various products, such as creams, lotions, and shampoos, where it may provide benefits like improved texture, enhanced stability, or specific therapeutic effects.
Used in Research and Development:
As a colorless liquid with distinct chemical properties, 2-butyloctanoic acid is an essential compound for research and development in various scientific fields. It can be used in the study of chemical reactions, the development of new materials, and the investigation of biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 27610-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,1 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27610-92:
(7*2)+(6*7)+(5*6)+(4*1)+(3*0)+(2*9)+(1*2)=110
110 % 10 = 0
So 27610-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-3-5-7-8-10-11(12(13)14)9-6-4-2/h11H,3-10H2,1-2H3,(H,13,14)
27610-92-0Relevant articles and documents
METHOD FOR PRODUCING HIGHER LINEAR FATTY ACIDS OR ESTERS
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, (2021/11/26)
The present invention relates to a method of producing linear fatty acids comprising 7 to 28 carbon atoms or esters thereof using a combined biotechnological and chemical method. In particular, the present invention relates to a method of producing dodecanoic acid (i.e. lauric acid), via higher alkanones, preferably 6-undecanone.
Improved synthesis and low-temperature performance of a series of saturated α-branched fatty acids
Jiang, Yang,Hu, Wenjing,Xu, Jian,Li, Jiusheng
, p. 2359 - 2363 (2017/10/06)
Five saturated α-branched fatty acids, also known as Guerbet acids, including α-propylhexyl acid (G 1 ), α-butylhexyl acid (G 2 ), α-propyloctyl acid (G 3 ), α-butyloctyl acid (G 4 ), and α-hexyloctyl acid (G 5 ), were synthesized in high yields by four-step reaction. Colorless, almost odorless, and oily products were obtained with high purity, whose structures were confirmed by GC, 1H/13C NMR, and ESI-MS characterization. G 1, G 3, and G 4 had pour points lower than -60 °C, while G 2 and G 5 showed higher pour points (-42 °C and 6 °C, respectively) because of their molecular symmetry. Considering the low-temperature properties, G 1, G 3, G 4, and even G 2 held great potential applications in the lubricant and oilfield.
