14936-66-4

Basic information

• Product Name: ACETIC ACID 2-NONYL ESTER
• Synonyms: (±)-2-Nonanolacetate;1-Methyloctylethanoate;2-Nonanol,acetate;ACETIC ACID 2-NONYL ESTER;ACETIC ACID 1-METHYLOCTYL ESTER;1-METHYLOCTYL ACETATE;2-NONYL ACETATE;EINECS 239-010-7
• CAS NO: 14936-66-4
• Molecular Formula: C₁₁H₂₂O₂
• Molecular Weight: 186.29
• EINECS: 239-010-7
• Mol File: 14936-66-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: -26°C (estimate)
• Boiling Point: 215 °C
• Flash Point: 82.9°C
• Appearance: /
• Density: 0.86
• Vapor Pressure: 0.158mmHg at 25°C
• Refractive Index: 1.4180-1.4200
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: ACETIC ACID 2-NONYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: ACETIC ACID 2-NONYL ESTER(14936-66-4)
• EPA Substance Registry System: ACETIC ACID 2-NONYL ESTER(14936-66-4)

Safety Data

• Hazardous Substances Data: 14936-66-4(Hazardous Substances Data)

Usage

General Description

ACETIC ACID 2-NONYL ESTER is an organic compound commonly used as a fragrance ingredient in various household and personal care products. It is also known for its use as a solvent in the manufacturing of paints, coatings, adhesives, and synthetic resins. This chemical is generally recognized as safe for use in food and is commonly used as a flavoring agent in the food industry. ACETIC ACID 2-NONYL ESTER is also used in the production of plasticizers and as a raw material in the synthesis of other chemicals. It is important to handle this chemical with care as it may cause irritation to the skin, eyes, and respiratory system upon exposure.

InChI:InChI=1/C11H22O2/c1-4-5-6-7-8-9-10(2)13-11(3)12/h10H,4-9H2,1-3H3

Upstream product

• 628-99-9 nonan-2-ol 
• 127-09-3 sodium acetate 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 211996-16-6 non-1-en-3-yn-2-yl acetate 
• 13125-66-1 n-heptylmagnesium bromide 
• 821-55-6 2-Nonanone 
• 124-11-8 non-1-ene 
• 64-19-7 acetic acid 
• 2216-35-5 2-bromononane 
• 563-63-3 silver(I) acetate 

Downstream Products

• 628-99-9 nonan-2-ol 
• 628-99-9 (R)-2-nonanol 
• 70419-06-6 (S)-nonan-2-ol 
• 117636-58-5 (R)-2-nonyl hexanoate 
• 117636-46-1 (R)-2-nonyl butanoate 

Relevant articles and documents

Novel sol-gel lipases by designed bioimprinting for continuous-flow kinetic resolutions

The bioimprinting effect in sol-gel immobilization of lipases was studied to develop efficient novel immobilized biocatalysts with significantly improved properties for biotransformations in continuous-flow systems. The bioimprinting candidates were selected systematically among the substrate mimics already found in the active site of experimental lipase structures. Four lipases (Lipase AK, Lipase PS, CaLB and CrL) were immobilized by a sol-gel process with nine bioimprinting candidates using various combinations of tetraethoxysilane (TEOS), phenyltriethoxysilane (PhTEOS), octyltriethoxysilane (OcTEOS) and dimethyldiethylsilane (DMDEOS) as silica precursors. The biocatalytic properties of the immobilized lipases were characterized by enantiomer selective acylation of various racemic secondary alcohols in two different multisubstrate systems (mixture A: a series of alkan-2-ols rac-1a-e and mixture B: heptan-2-ol rac-1f and 1-phenylethanol rac-1g). Except with Lipase AK, the most significant activity enhancement was found with the imprinting molecules already found as substrate mimics in X-ray structures of various lipases. The synthetic usefulness of the best biocatalysts was demonstrated by the kinetic resolution of racemic 1-(thiophen-2-yl)ethanol (rac-1h) in batch and continuous-flow systems. Copyright

Mg(ClO4)2 as a powerful catalyst for the acylation of alcohols under solvent-free conditions

A trace amount of magnesium perchlorate (from 0.1 mol% to 1 mol%) is able to promote quantitative acylation, with anhydrides, of a large variety of functionalized alcohols in short times, at room temperature and under solvent-free conditions.