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Decanedioic acid hydrogen 1-butyl ester, also known as sebacic acid hydrogen 1-butyl ester, is a chemical compound with the molecular formula C14H26O4. It is an ester derived from decanedioic acid (sebacic acid) and 1-butanol. This organic compound is characterized by its long-chain structure, consisting of a 10-carbon dicarboxylic acid and a 4-carbon alcohol. Decanedioic acid hydrogen 1-butyl ester is a colorless liquid with a low melting point and is soluble in most organic solvents. It is used in various applications, including as a plasticizer, a lubricant, and a component in the production of certain polymers and resins. The compound is also known for its potential use in the synthesis of other chemicals and as a precursor in the pharmaceutical industry.

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  • 5278-98-8 Structure
  • Basic information

    1. Product Name: Decanedioic acid hydrogen 1-butyl ester
    2. Synonyms: Decanedioic acid hydrogen 1-butyl ester;Sebacic acid hydrogen 1-butyl ester
    3. CAS NO:5278-98-8
    4. Molecular Formula: C14H26O4
    5. Molecular Weight: 258.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5278-98-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Decanedioic acid hydrogen 1-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Decanedioic acid hydrogen 1-butyl ester(5278-98-8)
    11. EPA Substance Registry System: Decanedioic acid hydrogen 1-butyl ester(5278-98-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5278-98-8(Hazardous Substances Data)

5278-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5278-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5278-98:
(6*5)+(5*2)+(4*7)+(3*8)+(2*9)+(1*8)=118
118 % 10 = 8
So 5278-98-8 is a valid CAS Registry Number.

5278-98-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Decanedioic acid monobutyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5278-98-8 SDS

5278-98-8Relevant articles and documents

Selective monoesterification of dicarboxylic acids catalysed by ion-exchange resins

Nishiguchi, Takeshi,Ishii, Yasuhiro,Fujisaki, Shizuo

, p. 3023 - 3027 (2007/10/03)

Symmetrical dicarboxylic acids with 4-14 carbon atoms gave selectively the corresponding monoesters in high yields in the transesterification catalysed by strongly acidic ion-exchange resins in ester-hydrocarbon mixtures. It was found that the rate of the esterification of the dicarboxylic acids is much higher than that of the monocarboxylic acids formed. This result can explain the high selectivity for the monoester formation and can also be explained by the existence of an aqueous layer on the surface of the resins. This method of selective esterification is quite simple and practical. The Royal Society of Chemistry 1999.

Convenient selective monoesterification of α, ω-dicarboxylic acids catalyzed by ion-exchange resins

Saitoh, Masahiko,Fujisaki, Shizuo,Ishii, Yasuhiro,Nishiguchi, Takeshi

, p. 6733 - 6736 (2007/10/03)

Symmetric dicarboxylic acids, ranging from pentanedioic acid to tetradecanedioic acid, gave selectively the corresponding monoesters in high yields in the transesterification catalyzed by strongly acidic ion-exchange resins in ester/octane mixtures.

SELECTIVE MONOETHERIFICATION AND MONOESTERIFICATION OF DIOLS AND DIACIDS UNDER PHASE-TRANSFER CONDITIONS

Zerda, Jaime de la,Barak, Gabriela,Sasson, Yoel

, p. 1533 - 1536 (2007/10/02)

Research on the selectivity of etherification reactions of diols and esterification reactions of diacids by alkyl halides under phase-transfer catalysis has shown that under such conditions, selectivity of monoetherification increases in the order prim sec tert diols, though overall yield of monoether decreases from sec to tert diols.Monoesterification of diacids was accomplished with a high degree of selectivity.Optimal extraction of diols and diacids was found to correspond in general to chain lengths of around 5 carbons.This could mean that the complex formed between the catalyst and the anion to react is stabilized for certain carbon lengths by inner solvation in virtue of its spatial conformation.

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