693-55-0

Basic information

• Product Name: ETHYL HYDROGEN SEBACATE
• Synonyms: ETHYL HYDROGEN SEBACATE;DECANEDIOIC ACID MONOETHYL ESTER;Decanedioic acid monoethyl ester~Monoethyl sebacate~Sebacic acid monoethyl ester;monoethyl sebacate;Monoethyl sebacate~Sebacic acid monoethyl ester;Ethylhydrogensebacate,Monoethylsebacate;Sebacicacidmonoethylester;Decanedioic acid 1-ethyl ester
• CAS NO: 693-55-0
• Molecular Formula: C₁₂H₂₂O₄
• Molecular Weight: 230.3
• EINECS: 211-753-1
• Product Categories: Miscellaneous
• Mol File: 693-55-0.mol
• Article Data: 12

Chemical Properties

• Melting Point: 35-38°C
• Boiling Point: 336℃
• Flash Point: 119℃
• Appearance: White Solid
• Density: 1.024
• Vapor Pressure: 2.17E-05mmHg at 25°C
• Refractive Index: 1.455
• BRN: 1782569
• CAS DataBase Reference: ETHYL HYDROGEN SEBACATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL HYDROGEN SEBACATE(693-55-0)
• EPA Substance Registry System: ETHYL HYDROGEN SEBACATE(693-55-0)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• TSCA: Yes
• Hazardous Substances Data: 693-55-0(Hazardous Substances Data)

Usage

General Description

Ethyl hydrogen sebacate is a chemical compound commonly used in the fragrance and flavor industry. It is a colorless to pale yellow liquid with a sweet, fruity odor. Ethyl hydrogen sebacate is primarily used as a flavoring agent in food products and as a scent enhancer in perfumes and cosmetic products. It is also used in the production of plasticizers, which are additives that improve the flexibility and durability of plastics. Additionally, ethyl hydrogen sebacate is used in the synthesis of other chemicals, such as pharmaceuticals and agricultural products. Overall, this chemical compound plays a vital role in various industries, particularly in enhancing the sensory qualities of consumer products.

InChI:InChI=1/C12H22O4/c1-2-16-12(15)10-8-6-4-3-5-7-9-11(13)14/h2-10H2,1H3,(H,13,14)

Upstream product

• 110-40-7 diethyl sebacate 
• 108-55-4 glutaric anhydride, 
• 25542-62-5 6-bromo-hexanoic acid ethyl ester 
• 64-17-5 ethanol 
• 106-79-6 dimethyl sebacate 
• 111-20-6 1,10-decanedioic acid 
• 79-21-0 peracetic acid 
• 692-86-4 ethyl 10-undecenenoate 

Downstream Products

• 14811-95-1 eicosa-1,19-diene 
• 18281-04-4 ethyl nonadecanoate 
• 1472-93-1 dimethyl 1,18-octadecanedioate 
• 1472-90-8 diethyl octadecanedioate 
• 28598-81-4 ethyl 9-bromononanoate 
• 6946-46-9 9-ethoxycarbonylnonanoic acid chloride 
• 257951-50-1 10-(2-hydroxy-4-methylanilino)-10-oxo-decanoic acid 
• 35194-39-9 ethyl non-8-enoate 
• 18490-59-0 ethyl 10-oxooctadecanoate 
• 638-26-6 10-hydroxystearic acid 
• 209962-97-0 10-(2-hydroxyanilino)-10-oxo-decanoic acid 
• 102707-65-3 12-<2-Carbomethoxy-phenyl>-dodecansaeure-(1)-methylester 
• 2388-78-5 11-oxododecanoic acid 
• 1120-10-1 9-chlorononanoic acid 

Relevant articles and documents

LIPIDS FROM THE BROWN ALGA CYSTOSEIRA BARBATA

Two new diunsaturated lipids, related to palmitic acid, were isolated from the brown alga Cystoseira barbata, one of which is toxic to mice during P388 lymphocytic leukemia tests. Key Word Index - Cystoseira barbata; Phaeophyceae; brown alga, ethyl-(Z),(Z)-hexadec-10,13-dienate; (Z),(Z)-hexadec-10,13-dienal.

Silica-Mediated Monohydrolysis of Dicarboxylic Esters

A new method for the monohydrolysis of dicarboxylic esters is presented, involving as key step a silanolysis at elevated temperatures at the silica gel surface. In the second step, the surface bound silyl esters are cleaved off under mild conditions, giving a straightforward and fast access to half esters. Based on recovered starting material generally yields well above 70 % are achieved, both, with stiff aromatic as well as flexible aliphatic substrates, as long as the ester groups involved are remote enough from each other. Otherwise competing reactions are becoming determinative, anhydride formation in the case of phthalates and decarbonylative fragmentation in the case of malonates. The new method was also successfully tested on a multigram scale with a minimalistic apparatus setup.

CATIONIC LIPID

The present invention provides a cationic lipid which can be utilized for nucleic acid delivery into the cytoplasm. The cationic lipid of the present invention is, for example, a compound represented by the following Formula (1) or a pharmaceutically acceptable salt thereof.