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2-(2,6-Dimethylhept-5-enyl)-1,3-dioxolane


  • CAS
  • Purity
  • 66512-92-3
  • 99%
Inquiry

Cost-effective and customizable 2-(2,6-Dimethylhept-5-enyl)-1,3-dioxolane 66512-92-3 for sale

  • Molecular Formula: C12H22O2
  • Molecular Weight: 198.305
  • Vapor Pressure: 0.028mmHg at 25°C 
  • Boiling Point: 254.3°Cat760mmHg 
  • Flash Point: 110.4°C 
  • PSA: 18.46000 
  • Density: 0.91g/cm3 
  • LogP: 3.13190 

2-(2,6-Dimethylhept-5-enyl)-1,3-dioxolane(Cas 66512-92-3) Usage

Natural Occurrence

Found in citrus fruits and lemongrass.

Physical State

Colorless liquid.

Aroma

Strong, citrusy scent.

Industrial Use

Widely used in fragrance and flavor industries.

Flavoring Agent

Used in foods and beverages.

Fragrance Use

Utilized in perfumes, soaps, and candles.

Antimicrobial Property

Effective against various microorganisms.

Insecticidal Property

Repels and eliminates insects.

Household & Personal Care

Popular ingredient in cleaning and care products.

Therapeutic Effects

Possesses anti-inflammatory, antioxidative, and anti-cancer properties.

General Description

2-(2,6-Dimethylhept-5-enyl)-1,3-dioxolane, also known as citral, is a natural compound commonly found in citrus fruits and lemongrass. It is a colorless liquid with a strong, citrusy scent and is widely used in the fragrance and flavor industries. Citral is used as a flavoring agent in foods and beverages and as a fragrance in perfumes, soaps, and candles. It also has antimicrobial and insecticidal properties, making it a popular ingredient in household and personal care products. Research has also shown potential therapeutic effects of citral, including anti-inflammatory, antioxidative, and anti-cancer properties.

InChI:InChI=1/C12H22O2/c1-10(2)5-4-6-11(3)9-12-13-7-8-14-12/h5,11-12H,4,6-9H2,1-3H3

66512-92-3 Relevant articles

Synthesis and characterization of some oxidized derivatives of citronellal ethylene acetal

Taylor, Wesley G.

, p. 1847 - 1852 (1982)

Three pairs of geometrical isomers corre...

Organocatalytic epoxidation and allylic oxidation of alkenes by molecular oxygen

Orfanidou, Maria,Petsi, Marina,Zografos, Alexandros L.

supporting information, p. 9172 - 9178 (2021/11/30)

Pyrrole-proline diketopiperazine (DKP) a...

AN EFFICIENT SbCl3-METAL SYSTEM FOR ALLYLATION, REDUCTION AND ACETALIZATION OF ALDEHYDES

Wang, Wei-Bo,Shi, Li-Lan,Huang, Yao-Zeng

, p. 3315 - 3320 (2007/10/02)

SbCl3-Fe or SbCl3-Al could induce allyla...

66512-92-3 Process route

3,7-dimethyl-oct-6-enal
106-23-0,26489-02-1

3,7-dimethyl-oct-6-enal

ethylene glycol
107-21-1

ethylene glycol

2-(2,6-dimethylhept-5-en-1-yl)-1,3-dioxolane
66512-92-3

2-(2,6-dimethylhept-5-en-1-yl)-1,3-dioxolane

Conditions
Conditions Yield
antimony(III) chloride; aluminium; for 20h; Ambient temperature;
92%
With camphor-10-sulfonic acid; orthoformic acid triethyl ester; In dichloromethane; at 20 ℃; for 12h; Inert atmosphere;
91%
With toluene-4-sulfonic acid; In benzene;
57.5%
2-(2,6-dimethylhept-5-en-1-yl)-1,3-dioxolane
66512-92-3

2-(2,6-dimethylhept-5-en-1-yl)-1,3-dioxolane

Conditions
Conditions Yield
Citronellal XV, Aethylenglykol/Benzol/p-Toluolsulfonsaeure;
(yield);

66512-92-3 Upstream products

  • 106-23-0
    106-23-0

    3,7-dimethyl-oct-6-enal

  • 107-21-1
    107-21-1

    ethylene glycol

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