- Chemical Name DIETHYL AZELATE
- CAS No. 624-17-9
- Contact Us Inquiry
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- Molecular Formula: C13H24 O4
- Molecular Weight: 244.331
- Vapor Pressure: 0.00194mmHg at 25°C
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Melting Point:
−16-−15.8 °C(lit.)
- Refractive Index: n20/D 1.435(lit.)
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Boiling Point:
172 °C18 mm Hg(lit.)
- Flash Point: >230°F
- PSA： 52.60000
- Density: 0.973g/mLat 25°C(lit.)
- LogP: 2.84330
DIETHYL AZELATE(Cas 624-17-9) Usage
|
General Description |
Diethyl azelate, also known as diethyl nonanedioate, is an ester compound with the chemical formula C12H22O4. It is a clear, colorless liquid with a fruity odor and is commonly used as a flavoring agent in food products. Diethyl azelate is also used as a fragrance ingredient in cosmetic and personal care products. It is considered to be a low-risk chemical with low acute toxicity and minimal environmental impact. However, it should still be handled with care and stored in a cool, dry place away from direct sunlight and heat sources. |
InChI:InChI=1/C13H24O4/c1-3-16-12(14)10-8-6-5-7-9-11-13(15)17-4-2/h3-11H2,1-2H3
624-17-9 Relevant articles
Lubricity, tribological and rheological properties of green ester oil prepared from bio-based azelaic acid
AHMED, WALED ABDO,SALIH, NADIA,SALIMON, JUMAT
, p. 1363 - 1369 (2021/06/09)
Plant oil derived compounds have been us...
The synthesis of di-carboxylate esters using continuous flow vortex fluidics
Britton, Joshua,Dalziel, Stuart B.,Raston, Colin L.
, p. 2193 - 2200 (2016/04/19)
A vortex fluidic device (VFD) is effecti...
Synthesis, antiproliferation, and docking studies of N-phenyl-lipoamide and 8-mercapto-N-phenyloctanamide derivatives: Effects of C6 position thiol moiety
Zhang, Shi-Jie,Hu, Wei-Xiao
, p. 3312 - 3320 (2012/11/07)
Some N-phenyl lipoamide and 8-mercapto- ...
METHODS AND COMPOSITIONS INVOLVING ESTERS OF AZELAIC ACID AND OTHER DICARBOXYLIC ACIDS
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Page/Page column 18-19, (2008/06/13)
The present invention relates to formula...
624-17-9 Process route
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123-99-9,26776-28-3
azelaic acid
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64-17-5
ethanol
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624-17-9
diethyl azelate
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
Heating / reflux;
|
88%
|
|
With
sulfuric acid;
at 20 ℃;
for 0.0541667h;
|
78%
|
|
With
phosphorus pentoxide; copper(II) sulfate; sodium sulfate;
for 2h;
Heating;
|
70%
|
|
With
hydrogenchloride;
|
|
|
With
sulfuric acid;
|
|
|
With
sulfuric acid;
durch Kochen unter azeotroper Destillation des entstehenden Wassers mit Toluol;
|
|
|
With
sulfuric acid;
durch Kochen unter azeotroper Destillation des entstehenden Wassers mit Benzol;
|
|
|
With
sulfuric acid;
|
|
|
With
sulfuric acid;
|
|
|
With
toluene-4-sulfonic acid;
In
toluene;
for 8h;
Reflux;
|
|
|
With
sulfuric acid;
In
toluene;
at 120 - 130 ℃;
for 4h;
Dean-Stark;
|
-
![(E)-3-[(1S,2R)-2-((E)-2-Ethoxycarbonyl-vinyl)-cyclopropyl]-acrylic acid ethyl ester](/upload/2026/5/2d24a5a2e0114208914d3850c9cbc49a_b403c369-5daf-4b89-ba87-d982a51b66ce.png)
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(E)-3-[(1S,2R)-2-((E)-2-Ethoxycarbonyl-vinyl)-cyclopropyl]-acrylic acid ethyl ester
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624-17-9
diethyl azelate
| Conditions | Yield |
|---|---|
|
With
hydrogen;
palladium on activated charcoal;
In
ethanol;
for 48h;
|
90%
|
624-17-9 Upstream products
-
123-99-9
azelaic acid
-
64-17-5
ethanol
-
1593-55-1
azelaic acid monoethyl ester
-
334-43-0
1-chloro-7-fluoro-heptane
624-17-9 Downstream products
-
502-49-8
cycloactanone
-
31067-25-1
1,9-diketocyclohexadecane
-
1593-55-1
azelaic acid monoethyl ester
-
3937-56-2
1,9-Nonanediol