Interesting facts
Interesting Facts about Diethyl Hexanedioate
Diethyl hexanedioate, often referred to as an ester, is renowned for its versatility and significance in both synthetic organic chemistry and industrial applications. Here are some compelling aspects of this compound:
- Synthesis: Diethyl hexanedioate can be synthesized through the reaction of diethyl malonate with a suitable acyl halide or by using a two-step condensation reaction. This process highlights the beauty of organic synthesis, allowing chemists to take simple building blocks and assemble complex structures.
- Applications: This compound is utilized as a intermediate in the production of various pharmaceuticals, fragrances, and plasticizers. The demand in these industries illustrates its importance in enhancing product characteristics, ranging from flavoring agents to materials properties.
- Structure and Properties: Diethyl hexanedioate features a backbone composed of a six-carbon chain with ester functional groups at both ends. This structure not only contributes to its reactivity but also impacts its physical properties, making it valuable for applications requiring specific solubility or volatility.
- Reactivity: As an ester, diethyl hexanedioate can undergo hydrolysis, transesterification, and other nucleophilic substitution reactions. These reactions are fundamental in organic chemistry, providing pathways to create new compounds or modify existing ones.
- Impact on Environment: Like many esters, diethyl hexanedioate is often studied for its environmental impact as well. Understanding its biodegradability and potential toxicity is crucial for sustainable product development.
In conclusion, diethyl hexanedioate stands as a prime example of the vital role that esters play in both environmental and synthetic chemistry. Its diverse applications and intriguing chemistry make it a fascinating subject for both students and established scientists. As one well-known chemist stated, "The connection between synthesis and application in chemistry reveals our capacity to innovate and create."
Synonyms
DIETHYL ADIPATE
141-28-6
Diethyl hexanedioate
Ethyl adipate
Hexanedioic acid, diethyl ester
1,6-Diethyl hexanedioate
Adipic acid, diethyl ester
Hexanedioic acid, 1,6-diethyl ester
ADIPIC ACID DIETHYL ESTER
Hexanedioic acid, diethyl-
Diethylester kyseliny adipove
Diethylhexanedioic acid
NSC 19160
Ethyl delta-carboethoxyvalerate
HSDB 5413
EINECS 205-477-0
Diethylester kyseliny adipove [Czech]
BRN 1780035
AI3-00342
DUB DEA
7B19K45L6C
NSC-19160
hexanedioic acid diethyl ester
DIETHYL ADIPATE [HSDB]
DTXSID2021999
Ethyl .delta.-carboethoxyvalerate
68201-71-8
WLN: 2OV4VO2
diethyladipate
UNII-7B19K45L6C
MFCD00009215
1,6Diethyl hexanedioate
Ethyl deltacarboethoxyvalerate
SCHEMBL50610
BIDD:ER0365
DIETHYL ADIPATE [INCI]
DTXCID201999
Diethyl adipate, >=99%, FG
CHEBI:34697
NSC3363
NSC-3363
NSC19160
Diethyl adipate, analytical standard
AKOS009031409
DS-5105
Diethyl adipate, ReagentPlus(R), 99%
A0162
NS00042075
EN300-19693
Diethyl adipate, Vetec(TM) reagent grade, 98%
Q27116229
F1905-6995
Z104474764
205-477-0
Solubility of Diethyl Hexanedioate
Diethyl hexanedioate, also known as diethyl adipate, has a unique solubility profile that is worth discussing. This compound is a diester derived from hexanedioic acid and is known for its moderate solubility in various solvents. Here are some key points regarding its solubility:
To summarize, diethyl hexanedioate showcases the typical behavior of larger diesters, being versatile among organic solvents while displaying limited solubility in water. Understanding these solubility characteristics is crucial for its practical applications in industrial and laboratory settings.