Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2442-49-1

Post Buying Request

2442-49-1 Suppliers

Recommended suppliersmore

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

2442-49-1 Usage

Description

Lignoceric acid methyl ester, also known as the methyl ester of lignoceric acid, is a wax-like solid esterified form of lignoceric acid. It has been identified in biodiesel produced from various types of animal fat and is characterized by its insolubility in water and solubility in alcohol and ether. Additionally, it is combustible.

Uses

Used in Analytical Chemistry:
Lignoceric acid methyl ester is used as an analytical reference standard for the determination of specific analytes in biodiesel produced from yellow horn oil using high-performance liquid chromatography (HPLC) technique.
Used in Gas Chromatography:
Lignoceric acid methyl ester serves as an external standard to study the pentafluorobenzylation reaction of estradiol in a biphasic methylene chloride/sodium hydroxide system, and in the absence of phase transfer agents, by gas chromatography (GC) technique.
Used in Special Synthesis:
Lignoceric acid methyl ester is utilized as an intermediate in special synthesis processes, contributing to the development of various chemical compounds.
Used in Biochemical Research:
LIGNOCERIC ACID METHYL ESTER is also employed as a reference standard in biochemical research, aiding in the study and understanding of biological processes and the development of new bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 2442-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2442-49:
(6*2)+(5*4)+(4*4)+(3*2)+(2*4)+(1*9)=71
71 % 10 = 1
So 2442-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C25H50O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25(26)27-2/h3-24H2,1-2H3

2442-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl tetracosanoate

1.2 Other means of identification

Product number -
Other names Tetracosanoic acid, methyl ester

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:2442-49-1 SDS

2442-49-1Downstream Products

2442-49-1Relevant articles and documents

Two amphoteric galactocerebrosides possessing a tri-unsaturated long-chain base from the leech (Hirudo nipponica)

Noda,Tanaka,Tsujino,Miura,Miyahara,Hayakawa

, p. 567 - 570 (1995)

Six amphoteric galactocerebrosides were isolated from the land annelid (Hirudo nipponica). Two of them have a tri-unsaturated long-chain base, D-erythro-(4E,8Z,11Z)-docosasphingatrienine. The position and geometry of the double bonds in the long-chain base unit were determined on the bases of chemical and spectral data.

Dammarane triterpenoids from Carnauba, Copernicia prunifera (Miller) H. E. Moore (Arecaceae), wax

De Almeida, Buana C.,Araújo, Bruno Q.,Barros, Elcio D. S.,Freitas, Samya D. L.,Maciel, Dayany S. A.,Ferreira, Ari J. S.,Guadagnin, Rafael C.,Vieira, Gerardo M.,Lago, Jo?o H. G.,Chaves, Mariana H.

, p. 1371 - 1376 (2017/07/13)

Phytochemical investigation from carnauba (Copernicia prunifera) wax led to the identification of sixteen dammarane–type triterpenes, including thirteen new characterized as: (24R*)-methyldammara-20,25-dien-3α-ol and a mixture of alkyl (24R*)-methyldammar-25-en-20-ol-3β-carboxylates, together with three previously described triterpenes: carnaubadiol, (24R*)-methyldammara-20,25-dien-3β-ol and (24R*)-24-methyldammara-20,25-dien-3-one. Moreover, four fatty alcohols (eicosanol, docosanol, tetracosanol and hexacosanol) as well as four sterols (cholesterol, campesterol, stigmasterol, and sitosterol) were also obtained. These compounds were isolated using classical chromatographic methods and their structures were determined by spectroscopic and chemical methods.

Nickel-butadiene catalytic system for the cross-coupling of bromoalkanoic acids with alkyl grignard reagents: A practical and versatile method for preparing fatty acids

Iwasaki, Takanori,Higashikawa, Kiyokazu,Reddy, Vutukuri P.,Ho, Willbe W. S.,Fujimoto, Yukari,Fukase, Koichi,Terao, Jun,Kuniyasu, Hitoshi,Kambe, Nobuaki

supporting information, p. 2956 - 2960 (2013/03/28)

The knights who say Ni: A practical and convenient synthetic route to fatty acids involves the Ni-catalyzed alkyl-alkyl cross-coupling of bromoalkanoic acids and alkyl Grignard reagents in the presence of 1,3-butadiene as an additive (see scheme). 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

What can I do for you?
Get Best Price

Get Best Price for 2442-49-1