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Heptadecane, 5-methylene-, also known as 5-methyleneheptadecane, is a chemical compound belonging to the alkane family. It is composed of 17 carbon atoms with a double bond located at the 5th position. This colorless liquid has a molecular formula of C18H36 and is commonly found in natural sources such as plants, insects, and marine organisms. With its low toxicity levels, Heptadecane, 5-methyleneis considered relatively safe for use in various industries.

57557-53-6

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57557-53-6 Usage

Uses

Used in Chemical Industry:
Heptadecane, 5-methyleneis used as a solvent for various chemical reactions due to its ability to dissolve a wide range of substances and facilitate the reaction process.
Used in Lubricant Industry:
Heptadecane, 5-methyleneis used as a lubricant in various applications, such as in machinery and engines, due to its low friction properties and ability to reduce wear and tear on moving parts.
Used in Fragrance Industry:
Heptadecane, 5-methyleneis used as a fragrance ingredient in perfumes, cosmetics, and other scented products due to its pleasant aroma and ability to blend well with other fragrance components.
Used in Research and Development:
Heptadecane, 5-methyleneis utilized in research and development for studying the properties and behavior of alkanes and their derivatives, as well as exploring potential applications in various fields.
Overall, Heptadecane, 5-methyleneis a versatile chemical compound with a wide range of applications across different industries, including chemical, lubricant, fragrance, and research and development, due to its unique properties and characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 57557-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,5 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57557-53:
(7*5)+(6*7)+(5*5)+(4*5)+(3*7)+(2*5)+(1*3)=156
156 % 10 = 6
So 57557-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H36/c1-4-6-8-9-10-11-12-13-14-15-17-18(3)16-7-5-2/h3-17H2,1-2H3

57557-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyl-1-tetradecene

1.2 Other means of identification

Product number -
Other names 2-Butyl-1-tetradecene

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:57557-53-6 SDS

57557-53-6Downstream Products

57557-53-6Relevant academic research and scientific papers

Cobalt-catalyzed dimerization of α-olefins to give linear α-olefin products

Broene, Richard D.,Brookhart, Maurice,Lamanna, William M.,Volpe Jr., Anthony F.

, p. 17194 - 17195 (2007/10/03)

[Cp*P(OMe)3CoCH2CH3]+ [BarF]-, generated by the addition of HBArF to Cp*P(OMe)3Co(ethene), catalyzes the oligomerization of 1-hexene to give dimers and trimers. When a deficit of the acid is used, linear α-olefin dimers are produced at the expense of trimeric products: e.g., 1-butene, 1-hexene, and 1-octene give 1-octene, 1-dodecene, and 1-hexadecene, respectively. Copyright

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