50373-29-0

Usage

Explanation

The International Union of Pure and Applied Chemistry (IUPAC) name for 1-Hexanol, 2-ethyl-, (R)-, which follows a standardized naming convention.

Explanation

The molecular formula represents the number of atoms of each element present in a molecule, in this case, 8 carbon (C), 18 hydrogen (H), and 1 oxygen (O) atoms.

Explanation

The compound exists in a liquid state at room temperature and is colorless, meaning it does not have any visible color.

Explanation

The compound has a pleasant, natural scent that can be described as a combination of floral and fruity notes.

Explanation

It is commonly used in the perfume and personal care industries as a component to create various fragrances.

Explanation

The compound serves as a solvent in chemical processes such as extraction and chromatography, which are techniques used to separate and analyze mixtures.

Explanation

It is used in the production of flavors and fragrances for the food, beverage, and cosmetic industries.

Explanation

The compound is utilized as a starting material for the synthesis of various chemicals.

Explanation

(R)-2-ethylhexan-1-ol has been studied for its potential as a biofuel due to its high energy density and low volatility.

Explanation

It is essential to handle this chemical with care, as it can cause harm if it is swallowed, breathed in, or touches the skin. Proper safety measures should be taken during its use and storage.

Physical State

Colorless liquid

Odor

Floral, fruity

Application

Fragrance ingredient

Application

Solvent in extraction and chromatography

Application

Flavor and fragrance manufacturing

Application

Raw material for chemical synthesis

Potential use

Biofuel

Safety Precaution

Harmful if ingested, inhaled, or comes into contact with the skin

Upstream product

• 108-05-4 vinyl acetate 
• 104-76-7 2-Ethylhexyl alcohol 

Downstream Products

• 18908-66-2 3-(bromomethyl)heptane 
• 1653-16-3 (-)(R)-3-iodomethyl-heptane 
• 393562-89-5 (Z)-but-2-enedioic acid mono[(R)-2-ethylhexyl] ester 
• 74746-55-7 di[(R)-2-ethylhexyl] phthalate 
• 18908-66-2 (-)-3-bromomethyl-heptane 
• 1418183-68-2 C₁₇H₂₆O₃ 
• 1418183-67-1 (R)-2-ethylhexyl (E)-3-[3-(benzyloxy)phenyl]acrylate 
• 1418196-09-4 C₁₇H₂₆O₃ 
• 1418183-66-0 (R)-2-ethylhexyl (E)-3-[2-(benzyloxy)phenyl]acrylate 
• 1116651-74-1 (4S,5R)-2-((R)-2-ethylhexylselanyl)-4-methyl-5-phenyl-4,5-dihydrooxazole 

Relevant academic research and scientific papers

Di[(R)-2-ethylhexyl] phthalate, a bioactive metabolite first isolated from three different bacillus species, and its synthesis

Di(2-ethylhexyl) phthalate (DEHP) is the most common phthalate ester, which has been used as a plasticizer for the production of numerous polymers, particularly polyvinyl chloride (PVC). Many other groups have synthesized meso-DEHP indicating interest in this molecule, but we are the first to synthesize enantiomerically pure di[(R)-2-ethylhexyl] phthalate. We report herein, for the first time, the isolation-from the cultures of Bacillus thuringiensis, B. subtilis, and B. velezensis strains-of di[(R)-2-ethylhexyl] phthalate, enantiomerically pure and in good yields: its biological activity against bacteria and fungi was probed and for the first time its synthesis was done.

Lipase-catalyzed transesterification of primary alcohols: Resolution of 2-ethylhexan-1-ol and 2-ethylhex-5-en-1-ol

Both the (R) and (S) enantiomers of 2-ethylhex-5-en-1-ol (R)-(-)-1, (S)-(+)-1 and 2-ethylhexan-1-ol (R)-(-)-2, (S)-(+)-2 were prepared in good yields and in high enantiomeric excess via lipase-catalyzed transacetylation of racemic alcohols 1 and 2 with vinyl acetate. Various experimental conditions (lipase PSL or PLF, solvent and temperature ranging from 30 to -30°C) are used and their influence on the enantioselectivity and on the reaction rate is evaluated. The (S) unsaturated alcohol 1 is specifically esterified by lipase PS in CH2Cl2 at 0°C with a very high enantiomeric ratio (E ～ 750) thus allowing the production of both enantiomers (R)-(-)-1 and (S)-(+)-1 with fairly good yields from the same enzymatic transformation. The comparison of unsaturated and saturated primary alcohols 1 and 2 shows that, for a similar atomic framework, the enantioselectivity of PSL is greatly enhanced by the presence of a terminal double bond. On the other hand, an enhancement of PSL enantioselectivity without loss of catalytic activity is achieved by decreasing the temperature to -30°C thus giving access to both enantiomers.