Welcome to LookChem.com Sign In|Join Free
  • or
Octadecanedioic acid, 1-methyl ester, also known as methyl stearate, is a colorless and odorless liquid that belongs to the class of carboxylic acid esters. It is soluble in organic solvents but insoluble in water. This chemical compound is relatively safe for use in consumer products when used as directed and in accordance with applicable regulations and guidelines.

72849-35-5

Post Buying Request

72849-35-5 Suppliers

Recommended suppliers

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

72849-35-5 Usage

Uses

Used in Cosmetics and Personal Care Products:
Octadecanedioic acid, 1-methyl ester is used as a fragrance ingredient in cosmetics, soaps, and other personal care products. Its pleasant scent and solubility in organic solvents make it a suitable ingredient for these applications.
Used in Chemical Manufacturing:
Octadecanedioic acid, 1-methyl ester serves as an intermediate in the manufacture of other chemicals. Its versatile chemical properties allow it to be used in the synthesis of various compounds.
Used in the Automotive Industry:
In the automotive industry, Octadecanedioic acid, 1-methyl ester is used as a lubricant additive. Its properties contribute to the performance and longevity of lubricants, enhancing the efficiency and durability of engines and machinery.

Check Digit Verification of cas no

The CAS Registry Mumber 72849-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72849-35:
(7*7)+(6*2)+(5*8)+(4*4)+(3*9)+(2*3)+(1*5)=155
155 % 10 = 5
So 72849-35-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H36O4/c1-23-19(22)17-15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18(20)21/h2-17H2,1H3,(H,20,21)

72849-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 18-methoxy-18-oxooctadecanoic acid

1.2 Other means of identification

Product number -
Other names Octadecandisaeure-mono-methylester

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:72849-35-5 SDS

72849-35-5Relevant academic research and scientific papers

Design, synthesis, and characterization of fatty acid derivatives of a dimeric peptide-based postsynaptic density-95 (PSD-95) inhibitor

Nissen, Klaus B.,Andersen, Julie J.,Haugaard-Kedstr?m, Linda M.,Bach, Anders,Str?mgaard, Kristian

, p. 1575 - 1580 (2015)

Dimeric peptide-based inhibitors of postsynaptic density-95 (PSD-95) can reduce ischemic brain damage and inflammatory pain in rodents. To modify the pharmacokinetic profile, we designed a series of fatty acid linked dimeric ligands, which potently inhibits PSD-95 and shows improved in vitro blood plasma stability. Subcutaneous administration in rats showed extended stability and sustained release of these ligands. This can facilitate new pharmacological uses of PSD-95 inhibitors and further exploration of PSD-95 as a drug target.

COMPOUND COMPRISING A NUCLEIC ACID AND A HALF-LIFE EXTENSION MOTIF

-

Paragraph 0852, (2021/06/04)

Disclosed herein are compounds including a nucleic acid (A), their preparation, and their use.

Preparation method of surfactant

-

Paragraph 0026; 0029, (2020/05/14)

The invention provides a preparation method of a surfactant, specifically comprising the following four steps: 1, preparing an intermediate 1 by using methyl oleate as a raw material; 2, letting the intermediate 1 firstly react with borane in a solvent, then oxidizing with hydrogen peroxide, and finally performing alkaline hydrolysis to obtain an intermediate 2; 3, jointly oxidizing the intermediate 2 into an intermediate 3 in a solvent by sodium hypochlorite, sodium perchlorate and TEMPO (2, 2, 6, 6-tetramethylpiperidine-1-oxy CAS number: 2564-83-2); and 4, hydrolyzing the intermediate 3 in asolvent under an alkaline condition, and acidifying to obtain the surfactant octadecanedioic acid. The preparation method is a synthetic method including four steps of chemical reactions, and can efficiently convert methyl oleate into octadecanedioic acid. The method is simple to operate; and the reagent is cheap and easily available, green and safe, efficient and environmentally-friendly, and suitable for industrial production.

Direct interaction, instrumental for signaling processes, between LacCer and Lyn in the lipid rafts of neutrophil-like cells

Chiricozzi, Elena,Ciampa, Maria Grazia,Brasile, Giuseppina,Compostella, Federica,Prinetti, Alessandro,Nakayama, Hitoshi,Ekyalongo, Roudy C.,Iwabuchi, Kazuhisa,Sonnino, Sandro,Mauri, Laura

, p. 129 - 141 (2015/03/05)

Lactosylceramide [LacCer; β-Gal-(1-4)-β-Glc-(1-1)-Cer] has been shown to contain very long fatty acids that specifically modulate neutrophil properties. The interactions between LacCer and proteins and their role in cell signaling processes were assessed

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 72849-35-5