27610-92-0

Basic information

• Product Name: 2-BUTYLOCTANOIC ACID
• Synonyms: 2-BUTYLOCTANOIC ACID;ISOLAURIC ACID;JARICTM I-12;2-butyl-octanoicaci;2-Butyloctansaeure;5-Undecanecarboxylic acid;5-undecanecarboxylicacid;BUTYLOCTANOIC ACID
• CAS NO: 27610-92-0
• Molecular Formula: C₁₂H₂₄O₂
• Molecular Weight: 200.32
• EINECS: 248-570-1
• Product Categories: C11 to C12;Carbonyl Compounds;Carboxylic Acids
• Mol File: 27610-92-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 230 °C(lit.)
• Flash Point: 113 °C
• Appearance: /
• Density: 0.887 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000174mmHg at 25°C
• Refractive Index: n20/D 1.438(lit.)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
• PKA: 4.82±0.40(Predicted)
• Water Solubility: 2.2mg/L at 20℃
• Stability: Stable. Incompatible with strong oxidizing agents. Combustible.
• CAS DataBase Reference: 2-BUTYLOCTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BUTYLOCTANOIC ACID(27610-92-0)
• EPA Substance Registry System: 2-BUTYLOCTANOIC ACID(27610-92-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 1
• RTECS: RH0368000
• Hazardous Substances Data: 27610-92-0(Hazardous Substances Data)

Usage

Chemical Properties

Colorless liquid

Uses

2-Butyloctanoic Acid is a fenton and photo-fenton oxidation of textile effluents.

General Description

2-Butyloctanoic acid is a 2-butyl-substituted carboxylic acid.

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)

Upstream product

• 927-49-1 dipentyl ketone 
• 142-62-1 hexanoic acid 
• 4941-53-1 5-undecene 
• 201230-82-2 carbon monoxide 
• 23708-56-7 6-undecanol 
• 67-56-1 methanol 
• 109-65-9 1-bromo-butane 
• 106-32-1 octanoic acid ethyl ester 
• 544-10-5 1-Chlorohexane 
• 111-25-1 1-bromo-hexane 
• 5659-17-6 3-butyl-4-pentylidene-oxetan-2-one 
• 3913-02-8 2-(n-butyl)octanol 

Downstream Products

• 5447-45-0 (1-butyl)heptyl bromide 
• 1442749-92-9 dimethyl 5-(2-butyloctanamido)isophthalic acid 
• 3913-02-8 2-(n-butyl)octanol 

Relevant articles and documents

METHOD FOR PRODUCING HIGHER LINEAR FATTY ACIDS OR ESTERS

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

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.