26118-61-6

Basic information

• Product Name: 1,10-DIACETOXYDECANE
• Synonyms: Bisacetic acid 1,10-decanediyl ester;Diacetic acid decane-1,10-diyl ester;Decamethylene Diacetate 1,10-Decanediol Diacetate;DECAMETHYLENE DIACETATE;1,10-DIACETOXYDECANE;1,10-DECANEDIOL DIACETATE
• CAS NO: 26118-61-6
• Molecular Formula: C₁₄H₂₆O₄
• Molecular Weight: 258.35
• EINECS: 247-471-0
• Mol File: 26118-61-6.mol

Chemical Properties

• Melting Point: 26 °C
• Boiling Point: 300.9°Cat760mmHg
• Flash Point: 26 °C
• Appearance: /
• Density: 0.969g/cm³
• Vapor Pressure: 0.00109mmHg at 25°C
• Refractive Index: 1.441
• CAS DataBase Reference: 1,10-DIACETOXYDECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-DIACETOXYDECANE(26118-61-6)
• EPA Substance Registry System: 1,10-DIACETOXYDECANE(26118-61-6)

Safety Data

• Hazardous Substances Data: 26118-61-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
1,10-DIACETOXYDECANE is used as a synthetic intermediate for the production of various organic compounds. Its versatile structure allows it to be a key component in the creation of a wide range of chemical products.
Used in the Food Industry:
1,10-DIACETOXYDECANE is used as a flavoring ingredient in the food industry. Its unique properties contribute to the development of flavors in food products, enhancing the overall taste experience for consumers.
Used in Pharmaceutical Industry:
Due to its distinctive chemical characteristics, 1,10-DIACETOXYDECANE has potential applications in the pharmaceutical industry. It may be utilized in the development of new drugs or as a component in existing medications, depending on its reactivity and compatibility with other compounds.
Used in Cosmetic Industry:
1,10-DIACETOXYDECANE also finds use in the cosmetic industry, where it may serve various functions such as a solvent, emulsifier, or preservative, thanks to its chemical properties that can be tailored to meet specific product requirements.
It is crucial to handle 1,10-DIACETOXYDECANE with care due to its potential health and environmental hazards if mismanaged. Proper safety measures and disposal methods should be strictly adhered to in all applications of 1,10-DIACETOXYDECANE.

InChI:InChI=1/C14H26O4/c1-13(15)17-11-9-7-5-3-4-6-8-10-12-18-14(2)16/h3-12H2,1-2H3

Upstream product

• 112-47-0 1,10-Decanediol 
• 75-36-5 acetyl chloride 
• 1600-27-7 mercury(II) diacetate 
• 4101-68-2 1,10-dibromodecane 
• 141-78-6 ethyl acetate 
• 552-86-3 furoin 
• 51490-07-4 1,2-di(furan-2-yl)ethanone 
• 1793-98-2 1,2-di(tetrahydrofuran-2-yl)ethane 
• 4464-77-1 1,2-di-furan-2-yl-ethane-1,2-diol 
• 64-19-7 acetic acid 
• 98-01-1 furfural 
• 5416-79-5 1,2-di(furan-2-yl)ethylene 
• 127-09-3 sodium acetate 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 1647-16-1 1,10-decadiene 
• 50816-18-7 9-decen-1-yl acetate 

Relevant articles and documents

A Rotaxane Scaffold for the Construction of Multiporphyrinic Light-Harvesting Devices

A sophisticated photoactive molecular device has been prepared by combining recent concepts for the preparation of multifunctional nanomolecules (click chemistry on multifunctional scaffolds) with supramolecular chemistry (self-assembly to prepare rotaxanes). Specifically, a clickable [2]rotaxane scaffold incorporating a free-base porphyrin stopper has been prepared and functionalized with ten peripheral Zn(II)-porphyrin moieties. Electrochemical investigations of the final compound revealed a peculiar behavior resulting from the intramolecular coordination of the Zn(II) porphyrin moieties to 1,2,3-triazole units. Finally, steady state investigations of the compound combining Zn(II) and free-base porphyrin moieties have shown that this compound is a light-harvesting device capable of channeling the light energy from the peripheral Zn(II)-porphyrin subunits to the core by singlet–singlet energy transfer.

Synthesis of 1,10-decanediol diacetate and 1-decanol acetate from furfural

A green and efficient method was developed for upgrading furfural to 1,10-decanediol diacetate and 1-decanol acetate. 92% yield of the acetates was obtained through the tandem benzoin condensation and hydrodeoxygenation reaction. During the benzoin condensation, furfural was catalyzed into furoin in a quantitative yield by the immobilized NHC catalyst under solvent-free conditions. After dissolving the furoin intermediate in acetic acid, the Sc(OTf)3and Pd/C catalytic system was introduced for hydrodeoxygenation. The effects of reaction factors have been investigated in detail and the hydrodeoxygenation process has been explored by1H-NMR and GC-MS.

Method for preparing sebacic acid ester and derivatives thereof (by machine translation)

. Uses the compound of the formula, as the raw material, in the acid solvent selective hydrodeoxygenation to obtain.decanediol and n-decanol: and the method (I) is characterized in that the product is cheap and easily available, product in yield, high in purity, and suitable for industrial production 1,10 - in a simple, process route . The product obtained by the method has the advantages of high yield, high yield and low pollution, to the environment, and the corresponding alcohol, is obtained by saponification reaction. (by machine translation)

Method for synthesizing 1,9-decadiene

The invention discloses a method for synthesizing 1,9-decadiene. The method sequentially comprises the following steps: adding carboxylic acid and 1,10-decadienol into a reaction container, heating the container until the 1,10-decadienol is dissolved, adding a catalyst, carrying out an esterification reaction at 120-200 DEG C, and collecting water evaporated in the esterification reaction; continuously heating the container to 300-350 DEG C after no water is produced in the esterification reaction, carrying out a reaction for 5-8 h, and evaporating and collecting a mixed solution of 1,9-decadiene and carboxylic acid; and respectively post-processing the mixed of 1,9-decadiene and carboxylic acid to obtain carboxylic acid and 1,9-decadiene respectively. The method for preparing 1,9-decadiene is efficient, economical and green, and meets industrial production requirements.

Molecular iodine in isopropenyl acetate (IPA): a highly efficient catalyst for the acetylation of alcohols, amines and phenols under solvent free conditions

Iodine in isopropenyl acetate (IPA) is a highly efficient catalyst for the acetylation of a variety of alcohols, phenols and amines under solvent free conditions. Primary, secondary, tertiary alcohols, amines and mono to polyhydroxy phenols and anilines with electron donating or withdrawing substituents can be easily acetylated in good to excellent yield at 85-90 °C.

Process for preparing monoesters

A process for preparing monoesters comprises the step of reacting at least one diol with at least one carboxylic acid in a biphasic solvent system, the carboxylic acid being sufficiently water soluble to allow esterification to occur, and the biphasic solvent system comprising water and at least one aprotic solvent in which the resulting monoester has greater solubility than in water.

Facile and highly selective monoacylation of symmetric diols adsorbed on silica gel with acetyl chloride

Monoacetylated alcohols of symmetric 1,n-diols are synthesized quantitatively by refluxing a suspension of the diols adsorbed on silica gel with acetylchloride.

Mercury-assisted solvolyses of alkyl halides. Simple procedures for the preparation of nitrate esters, acetate esters, alcohols and ethers

The reactions of a wide variety of alkyl halides with mercury(I) and/or (II) nitrate in 1,2-dimethoxyethane, mercury(II) acetate in acetic acid, aqueous mercury(II) perchlorate, and mercury(II) perchlorate in alcohol solvents have been investigated; as a result, simple high yield procedures for the conversion of alkyl halides into the corresponding nitrate esters, acetate esters, alcohols and ethers have been developed.