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E-2-OCTADECENAL, also known as (E)-2-octadecenal, is a naturally occurring aldehyde that is commonly found in various plants and insects. It is characterized by a long hydrocarbon chain with a double bond at the second carbon and an aldehyde functional group at the end. This organic compound is known for its distinct odor and is used in various applications due to its unique properties.

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  • 51534-37-3 Structure
  • Basic information

    1. Product Name: E-2-OCTADECENAL
    2. Synonyms: E-2-OCTADECENAL;(2E)-Octadecenal;Koiganal I;trans-2-Octadecenal
    3. CAS NO:51534-37-3
    4. Molecular Formula: C18H34O
    5. Molecular Weight: 266.46
    6. EINECS: N/A
    7. Product Categories: Aliphatics
    8. Mol File: 51534-37-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 364.1°C at 760 mmHg
    3. Flash Point: 187.1°C
    4. Appearance: /
    5. Density: 0.841g/cm3
    6. Vapor Pressure: 1.72E-05mmHg at 25°C
    7. Refractive Index: 1.453
    8. Storage Temp.: -20°C Freezer
    9. Solubility: Acetone (Slightly), Chloroform (Slightly), Ethyl Acetate (Slightly)
    10. CAS DataBase Reference: E-2-OCTADECENAL(CAS DataBase Reference)
    11. NIST Chemistry Reference: E-2-OCTADECENAL(51534-37-3)
    12. EPA Substance Registry System: E-2-OCTADECENAL(51534-37-3)
  • 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: 51534-37-3(Hazardous Substances Data)

51534-37-3 Usage

Uses

Used in Pheromone Production:
E-2-OCTADECENAL is used as a sex pheromone for attracting mates in several species of insects. It plays a crucial role in the reproductive behavior of these species, as the release of E-2-OCTADECENAL helps in the identification and attraction of potential mates.
Used in Fragrance Industry:
E-2-OCTADECENAL is used as a fragrance ingredient in the perfumery and cosmetics industry. Its distinct and pleasant odor makes it a valuable addition to various fragrance formulations, enhancing the overall scent profile of perfumes, colognes, and other scented products.
Used in Insect Attractants:
In the agricultural and pest control industries, E-2-OCTADECENAL is used as an attractant to lure specific insect species. By mimicking the natural pheromones of these insects, it can be employed in trapping and monitoring systems to control pest populations and protect crops.
Used in Chemical Research:
E-2-OCTADECENAL is also utilized in chemical research and development, particularly in the synthesis of various organic compounds and materials. Its unique structure and functional groups make it a versatile building block for creating new molecules with potential applications in various fields, such as pharmaceuticals, materials science, and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 51534-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51534-37:
(7*5)+(6*1)+(5*5)+(4*3)+(3*4)+(2*3)+(1*7)=103
103 % 10 = 3
So 51534-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h16-18H,2-15H2,1H3/b17-16+

51534-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E,Z)-2,13:octadecadienal

1.2 Other means of identification

Product number -
Other names (2E)-Octadecenal

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:51534-37-3 SDS

51534-37-3Downstream Products

51534-37-3Relevant articles and documents

A short synthesis of an acetylenic alcohol from the sponge cribrochalina vasculum

Gung, Benjamin W.,Dickson, Hamilton D.,Seggerson, Sara,Bluhm, Kristin

, p. 2733 - 2740 (2002)

A short synthesis of the acetylenic alcohol from cribrochalina vasculum is described. No protecting groups are used in this synthesis. The key step is an enzymatic resolution of a racemic mixture of the title compound.

Pheromone synthesis, CLXXV: Synthesis of koiganal I and II, the sex pheromone components of the webbing clothes moth

Takikawa, Hirosato,Takenaka, Motonobu,Mori, Kenji

, p. 139 - 140 (2007/10/03)

Koiganal I [(E)-2-octadecenal (1)] and II [(2E,13Z)-2,13-octadecadienal (2)], the female-produced pheromone components of the webbing clothes moth (Tineola bisselliella), were synthesized. VCH Verlagsgesellschaft mbH, 1997.

A Facile and Highly Stereoselective Synthesis of Trichonine by Two Consecutive Reactions of Arsonium Salts

Shi, Lilan,Yang, Jianhua,Li, Ming,Huang, Yao-Zeng

, p. 377 - 378 (2007/10/02)

Trichonine (5) has been synthesized from 1-hexadecanal (1) by two steps of consecutive olefination, in which formylmethyltriphenylarsonium bromide (2) and (pyrrolidinecarbonyl)methyltriphenylarsonium bromide (4) were used in the presence of potassium carbonate.The product was obtained in pure (2E,4E) configuration, and the overall yield reached 87percent.

ANION OF 1--2-PHENYLSULFONYLCYCLOPROPANE AS A NEW d3-REAGENT: PREPARATION OF β-SUBSTITUTED α,β-UNSATURATED ALDEHYDES

Pohmakotr, Manat,Pisutjaroenpong, Somchai

, p. 3613 - 3616 (2007/10/02)

Preparation of β-alkylsubstituted α,β-unsaturated aldehydes using a new d3-reagent is described.

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