Welcome to LookChem.com Sign In|Join Free
  • or
Heptadecane, 9-methyleneis a chemical compound composed of seventeen carbon atoms with a methylene carbon group (CH2) at the ninth position. It is a type of hydrocarbon found in natural sources such as plants, animals, and petroleum.

51655-66-4

Post Buying Request

51655-66-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

51655-66-4 Usage

Uses

Used in Industrial Applications:
Heptadecane, 9-methyleneis used as a solvent, lubricant, and in the production of polymers and plastics due to its chemical properties and versatility in various processes.
Used in Biodiesel Fuel Additives:
Heptadecane, 9-methyleneis considered for use as a biodiesel fuel additive because of its high energy content and low emissions, which can potentially improve fuel efficiency and reduce environmental impact.
Used in Plant Protection:
Heptadecane, 9-methyleneis found as a constituent of the waxy coating on the leaves of some plant species, where it serves as a protective layer against dehydration and environmental stress, contributing to the plant's overall health and survival.

Check Digit Verification of cas no

The CAS Registry Mumber 51655-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,5 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51655-66:
(7*5)+(6*1)+(5*6)+(4*5)+(3*5)+(2*6)+(1*6)=124
124 % 10 = 4
So 51655-66-4 is a valid CAS Registry Number.

51655-66-4SDS

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 9-methylideneheptadecane

1.2 Other means of identification

Product number -
Other names Heptadecane,9-methylene

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:51655-66-4 SDS

51655-66-4Downstream Products

51655-66-4Relevant academic research and scientific papers

Behavior of protonated cyclopropyl intermediates during polyalphaolefin synthesis: Mechanism and predicted product distribution

Gee, Jeffrey C.,Small, Brooke L.,Hope, Kenneth D.

, p. 1409 - 1417 (2012)

A new mechanism for the origin of multiple skeletal isomers observed in the cationic dimerization of 1-decene is proposed, and products that should form based on this mechanism are predicted. A protonated cyclopropyl intermediate appeared to form directly from combination of 2-decyl carbocation with 1-decene; formation of this intermediate did not appear to occur via ring closure of a branched secondary carbocation. The authors propose that rapid, repeated isomerizations of the protonated cyclopropyl intermediates lead to multiple skeletal isomers in decene dimers. The proposed mechanism can account for structures previously identified in mixtures of decene dimers and butene dimers. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 51655-66-4