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1,3-Nonanediol acetate(CAS#1322-17-4)

Chemical Property:

Molecular Formula C11H22O3
Molar Mass 202.29
Density 0.959 g/mL at 25 °C(lit.)
Boling Point 265 °C(lit.)
Flash Point 230 °F
Refractive Index n20/D 1.446(lit.)
Physical and Chemical Properties Chemical properties colorless or yellowish oily liquid. Relative density 0.960-970, refractive index 1.4400-1.4500, flash point above 100 ℃, soluble in 4 volumes of 60% ethanol or 2 volumes of 70% ethanol, soluble in oily spices. It has a strong and fresh breath like jasmine, with a slight fragrance of oily herbs, strong aroma, and general persistence.
Use Widely used as the matrix of jasmine, can be introduced into the oil herb, is the characteristic aroma of the large flower jasmine net oil, stable and strong diffusion force, very suitable for soap flavor, lavender type is also very good. It can also be used for food flavor, such as for berries and fresh fruit compound.

Product Detail

Product Tags

WGK Germany 2

 

 

1,3-Nonanediol acetate(CAS#1322-17-4) introduce

nature
Jasmine ester is an organic compound.
It is relatively stable in air, but unstable under strong acid and alkali conditions.
It is also a flammable substance and requires attention to fire prevention measures when storing and handling.

Application and synthesis method
Jasmine ester is an organic compound. It has the fragrant smell of jasmine, and is widely used as a component of spice and essence.

There are various methods for synthesizing jasmonate. Jasmine ester is usually synthesized by reacting jasmine alcohol with acetic acid. The specific steps are as follows:
Add jasmine alcohol and acetic acid into the reaction vessel;
Esterification reaction can be carried out at an appropriate temperature using acid catalysts such as sulfuric acid or zinc chloride;
After the reaction is complete, extract the obtained jasmonate by distillation or other separation methods.

Jasmine esters can also be obtained through other synthetic routes, such as using ester exchange reactions or catalytic hydrogenation reactions to convert related compounds.


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