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CAS

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67715-81-5

1,4-Nonanediol, diacetate is an organic compound with the chemical formula C11H20O4. It is a diester derived from 1,4-nonanediol, where two hydroxyl groups are esterified with acetic acid. This colorless liquid is soluble in organic solvents and has a molecular weight of 216.28 g/mol. It is used as a synthetic intermediate in the production of various chemicals, including fragrances and pharmaceuticals, due to its ability to form esters with other compounds. The compound is characterized by its ester functional groups, which contribute to its reactivity and potential applications in chemical synthesis.

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  • 67715-81-5 Structure

  • Basic information

    1. Product Name: 1,4-Nonanediol, diacetate
    2. Synonyms: 1,4-Nonanediol, diacetate
    3. CAS NO:67715-81-5
    4. Molecular Formula: C13H24O4
    5. Molecular Weight: 244.3273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67715-81-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 311.9°Cat760mmHg
    3. Flash Point: 144.3°C
    4. Appearance: /
    5. Density: 0.975g/cm3
    6. Vapor Pressure: 0.000547mmHg at 25°C
    7. Refractive Index: 1.438
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,4-Nonanediol, diacetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,4-Nonanediol, diacetate(67715-81-5)
    12. EPA Substance Registry System: 1,4-Nonanediol, diacetate(67715-81-5)

  • 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: 67715-81-5(Hazardous Substances Data)

67715-81-5 Usage

Primary Uses

Plasticizer, solvent, and fragrance ingredient

Derivation

Derived from 1,4-Nonanediol, a diol compound made from petrochemical sources

Formation

Esterifying both hydroxyl groups of the nonanediol with acetic acid

Physical Properties

Clear, colorless liquid with a fruity odor

Application in Polymers

Used in the production of vinyl, PVC, and other polymer products to improve flexibility and durability

Application as a Solvent

Used in various industrial and consumer applications

Application in Fragrances

Used as a fragrance ingredient in personal care and household products

Safety Precautions

Important to handle and use with proper safety measures due to potential hazards if not handled properly

Check Digit Verification of cas no

The CAS Registry Mumber 67715-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,1 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67715-81:
(7*6)+(6*7)+(5*7)+(4*1)+(3*5)+(2*8)+(1*1)=155
155 % 10 = 5
So 67715-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O4/c1-4-5-6-8-13(17-12(3)15)9-7-10-16-11(2)14/h13H,4-10H2,1-3H3

67715-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-diacetoxy-nonane

1.2 Other means of identification

Product number -
Other names 1,4-Diacetoxy-nonan

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:67715-81-5 SDS

67715-81-5Downstream Products

67715-81-5Relevant articles and documents

ACTIVATION OF CARBOXYL GROUPS BY DIPHENYL 2-OXO-3-OXAZOLINYLPHOSPHONATE. FACILE PREPARATION OF VERSATILE REAGENTS, 3-ACYL-2-OXAZOLONES

Kunieda, Takehisa,Higuchi, Tsunehiko,Abe, Yoshihiro,Hirobe, Masaaki

, p. 3253 - 3260 (2007/10/02)

Synthetic utility of the 2-oxazolone moiety as an excellent new leaving group is described.Based on such a function of the heterocycles, diphenyl 2-oxo-3-oxazolinylphosphonate has been newly introduced as a carboxyl-activating reagent which permits a facile direct preparation of 3-acyl-2-oxazolones and amides including peptides from a wide variety of carboxylic acids.The 3-acyl-2-oxazolides also serve as versatile reactive agents for highly chemoselective acyl-transfer to the nucleophilic species such as amines, alcohols and thiols, providing convenient and high-yield routes to amides, esters and thiol esters under mild conditions.They are also useful intermediates for ketones and alcohols.

HIGHLY SELECTIVE ACYLATION OF AMINES AND ALCOHOLS BY POLY(3-ACYL-2-OXAZOLONE)

Kunieda, Takehisa,Higuchi, Tsunehiko,Abe, Yoshihiro,Hirobe, Masaaki

, p. 1159 - 1160 (2007/10/02)

Poly(3-acyl-2-oxazolone) serves as a convenient reagent for highly chemo- and regioselective acylation of polyamines, amino-alcohols and polyalcohols.

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