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CAS

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39924-26-0

(Z)-oct-4-enal, also known as trans-4-octenal, is a colorless liquid chemical compound with the molecular formula C8H14O. It is characterized by a strong, fatty, waxy odor and is known for its green, fatty flavor profile. (Z)-oct-4-enal is naturally found in various fruits, vegetables, and plant aromas, and is valued for its potential antimicrobial and antioxidant properties, making it a versatile compound of interest across different industries.

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  • 39924-26-0 Structure

  • Basic information

    1. Product Name: (Z)-oct-4-enal
    2. Synonyms: (Z)-oct-4-enal;(Z)-4-Octenal;cis-4-Octenal
    3. CAS NO:39924-26-0
    4. Molecular Formula: C8H14O
    5. Molecular Weight: 126.19616
    6. EINECS: 254-701-3
    7. Product Categories: N/A
    8. Mol File: 39924-26-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 175℃
    3. Flash Point: 51℃
    4. Appearance: /
    5. Density: 0.832
    6. Vapor Pressure: 1.2mmHg at 25°C
    7. Refractive Index: 1.432
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (Z)-oct-4-enal(CAS DataBase Reference)
    11. NIST Chemistry Reference: (Z)-oct-4-enal(39924-26-0)
    12. EPA Substance Registry System: (Z)-oct-4-enal(39924-26-0)

  • 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: 39924-26-0(Hazardous Substances Data)

39924-26-0 Usage

Uses

Used in Food and Beverage Industry:
(Z)-oct-4-enal is used as a flavoring agent for its green, fatty flavor, enhancing the taste profiles of various food and beverage products.
Used in Fragrance Industry:
In the fragrance industry, (Z)-oct-4-enal is utilized for its vegetative and green notes, contributing to the creation of natural and refreshing scents in perfumes and other scented products.
Used in Antimicrobial Applications:
Due to its potential antimicrobial properties, (Z)-oct-4-enal can be employed as a natural preservative in various products to inhibit the growth of microorganisms, extending shelf life and ensuring safety.
Used in Antioxidant Applications:
Leveraging its antioxidant properties, (Z)-oct-4-enal can be used in the development of products aimed at preventing oxidation, which is crucial in industries such as food and cosmetics to maintain product quality and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 39924-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,2 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39924-26:
(7*3)+(6*9)+(5*9)+(4*2)+(3*4)+(2*2)+(1*6)=150
150 % 10 = 0
So 39924-26-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O/c1-2-3-4-5-6-7-8-9/h4-5,8H,2-3,6-7H2,1H3/b5-4+

39924-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name oct-4-enal

1.2 Other means of identification

Product number -
Other names (Z)-4-Octenal

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:39924-26-0 SDS

39924-26-0Downstream Products

39924-26-0Relevant articles and documents

OZONOLYSIS OF ALKENES AND REACTIONS OF POLYFUNCTIONAL COMPOUNDS. XXXV. SYNTHESIS OF 8Z-DODECENYL- AND 11Z-TETRADECENYL ACETATES FROM THE CYCLIC DIMER OF BUTADIENE

Odinokov, V. N.,Ishmuratov, G. Yu.,Galeeva, R. I.,Kharisov, R. Ya.,Sokol'skaya, O. V.,at al.

, p. 646 - 651 (2007/10/02)

The stereoselective synthesis of 8Z-dodecenyl- and 11Z-tetradecenyl acetates which are components of the sex pheromones of many species of insect of the order Lepidoptera, was realized on the basis of the partial ozonolysis of (Z,Z)-1,5-cyclooctadiene and its isomerization product (Z,Z)-1,3-cyclooctadiene.

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