41433-81-2

Basic information

• Product Name: DIETHYL N-HEXADECYLMALONATE
• Synonyms: DIETHYL N-HEXADECYLMALONATE;DIETHYL HEXADECYLMALONATE;2-hexadecyl-malonicaciddiethylester;Diethyl 2-hexadecylmalonate;hexadecyl-propanedioicaciddiethylester;Propanedioic acid, hexadecyl-, diethyl ester;n-Hexadecylmalonic acid diethyl ester;DIETHYL N-HEXADECYLMALONATE: TECH., 90%
• CAS NO: 41433-81-2
• Molecular Formula: C₂₃H₄₄O₄
• Molecular Weight: 384.59
• EINECS: 255-364-5
• Mol File: 41433-81-2.mol
• Article Data: 18

Chemical Properties

• Melting Point: 24-27°C
• Boiling Point: 204-208°C 2mm
• Flash Point: 178.9°C
• Appearance: /
• Density: 0.9118
• Vapor Pressure: 1.15E-06mmHg at 25°C
• Refractive Index: 1.4445
• CAS DataBase Reference: DIETHYL N-HEXADECYLMALONATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHYL N-HEXADECYLMALONATE(41433-81-2)
• EPA Substance Registry System: DIETHYL N-HEXADECYLMALONATE(41433-81-2)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 41433-81-2(Hazardous Substances Data)

Usage

General Description

Diethyl N-hexadecylmalonate is a chemical compound that is classified as an ester. It is commonly used as a flavoring agent and fragrance ingredient in various consumer products such as perfumes, soaps, and cosmetics. This chemical is also used in the manufacturing of pharmaceuticals and as a lubricant in the production of plastics and rubbers. Diethyl N-hexadecylmalonate is known for its fruity and floral scent, making it a popular choice for adding fragrance to a wide range of products. Additionally, it has been found to have potential antioxidant and antimicrobial properties, making it a versatile ingredient in various industries. However, it is important to handle this chemical with care and follow safety guidelines due to potential hazards associated with its use.

InChI:InChI=1/C23H44O4/c1-4-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22(24)26-5-2)23(25)27-6-3/h21H,4-20H2,1-3H3

Upstream product

• 996-82-7 sodium diethylmalonate 
• 112-82-3 hexadecanyl bromide 
• 111-61-5 stearic acid ethyl ester 
• 141-52-6 sodium ethanolate 
• 105-58-8 Diethyl carbonate 
• 105-53-3 diethyl malonate 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 1221575-18-3 2-[(hexadecylamino)carbonyl]octadecanoic acid 
• 89547-15-9 2-hexadecyloctadecanoic acid 
• 4371-64-6 n-hexadecylmalonic acid 
• 91662-79-2 1-O-Benzyl-2-n-hexadecylpropan-1,3-diol-3-phosphorsaeure-2'-bromethylester 
• 91662-78-1 1-O-Benzyl-2-n-hexadecylpropan-1,3-diol 
• 96563-17-6 4,4'-(2-hexadecyl-1,3-propanediyl)bis<10-<(4-methylphenyl)sulfonyl>-1,7-dioxa-4,10-diazacyclododecane> 
• 96563-16-5 2-hexadecylpropane-1,3-diol bis(4-methylbenzenesulfonate) 

Relevant articles and documents

Synthesis, characterization and blood compatibilities of novel segmented polyurethanes containing poly (butadiene) soft segments and phosphatidylcholine analogues in the main chains and long-chain alkyl groups in the side chains

New segmented polyurethanes (SPUs) containing poly(butadiene) (PBD) soft segments and phospholipid moieties in the main chains and long-chain alkyl groups in the side chains were synthesized. The phospholipid moieties include bis [2-(2-hydroxyethyldimethylammonio)ethyl] 2-octylpropane- 1,3-diyl bis(phosphate) (OcPDP), bis [2-(2-hydroxyethyldimethylammonio)ethyl]2- oleylpropane-1,3-diyl bis (phosphate) (O1PDP) and bis[2-(2- hydroxyethyldimethylammonio)ethyl] 2-cetylpropane-1,3-diyl bis(phosphate) (CPDP). The bulk characterization of synthesized SPUs was investigated by infrared (IR) spectroscopy and gel-permeation chromatography (GPC). The mechanical properties were evaluated by dynamic viscoelasticity and tensile measurements. The existence of phospholipid analogous groups on the surface of these SPUs was revealed by attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS) and contact angle measurements. The blood compatibilities of the new polymers were evaluated by platelet rich plasma (PRP) contact studies and viewed by scanning electron microscopy (SEM) using medical grade BioSpan and non- phospholipid polyurethane as references. These new materials have good surfaces in terms of platelet adhesion, and the morphology of adhered platelets undergoes a relatively low degree of variation.

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Synthesis of new lipophilic Ortho-dicarboranes

The synthesis of several new lipoidal dicarborane compounds prepared by reaction of decaborane with several fatty mona- and bis-alkyl-1,3-diols is described.

4'-HALOGEN CONTAINING NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO

Disclosed are halogen containing nucleotide and nucleoside therapeutic compositions and uses related thereto. In certain embodiments, the disclosure relates to the treatment or prophylaxis of viral infections. Such viral infections can include tongaviridae, bunyaviridae, arenaviridae, coronaviridae, flaviviridae, picornaviridae, Eastern, Western, and Venezuelan Equine Encephalitis (EEE, WEE and VEE, respectively), Chikungunya fever (CHIK), Ebola, Influenza, RSV, and Zika virus infections.

NOVEL XYLENE-BASED AMPHIPHILIC COMPOUND AND USE THEREOF

The present invention relates to a xylene-based amphiphilic compound, a method for preparing the same, and a method for extracting, solubilizing, stabilizing or crystallizing a membrane protein using the same. By using the xylene-based compound according to the present invention, a membrane protein may be stably stored in an aqueous solution for a long time, and may be applied in functional and structural analyses. The structural and functional analysis of the membrane protein is one of the fields of highest interest in biology and chemistry, and the xylene-based compound according to the present invention can be applied in research on protein structure that is closely related to development of a new drug.