Octadecylacrylat

Stearyl acrylate

HCID 62552CAS 4813-57-4

Grundinformationen

Standard-SMILES
C=CC(=O)OCCCCCCCCCCCCCCCCCC
InChIKey
FSAJWMJJORKPKS-UHFFFAOYSA-N
Summenformel
C21H40O2
Durchschnittliche Molmasse
324,5 g/mol
Monoisotopische Masse
324,30283052

Überblick

See also: Stearyl acrylate polymer (110000 MW) (monomer of).

Namen und Bezeichner

Bevorzugter Name
Stearyl acrylate
IUPAC
octadecyl prop-2-enoate
Lokaler Name
Octadecylacrylat
Englischer Name
Octadecyl acrylate
Summenformel
C21H40O2
Molmasse
324.54

Namen und Synonyme

Octadecyl acrylate4813-57-4Stearyl acrylaten-Octadecyl acrylate2-Propenoic acid, octadecyl esterOctadecyl 2-propenoateL37WJG7RTHBLEMMER SAEXCEPARL SUNII-L37WJG7RTHLIGHT ACRYLATE S-AEINECS 225-383-3
Weitere Namen anzeigen
Octadecyl2-propenoate60%C18,20%C16OctadecylacrylatAcrylic acid octadecyloctadecyl prop-2-enoateStearyl acrylate COA TDSACRYLIC ACID STEARYL ESTER
VISCOAT STAAI3-15687EC 225-383-3Acrylic acid, octadecyl ester1-OCTADECANOL, ACRYLATEDTXSID9063613RefChem:9276DTXCID2040608

Datenbank-Bezeichner

CAS
4813-57-4
PubChem CID
62552
DTXSID
DTXSID9063613
UNII
L37WJG7RTH
EC Number
225-383-3
Nikkaji
J82.109H

Eigenschaften

Berechnete Struktureigenschaften

XLogP
9,4
Polarare Oberfläche (TPSA)
26,3 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
19
Schwere Atome
23

Experimentelle und physikochemische Eigenschaften

LogP7.1
Physical DescriptionLiquid; Other Solid; Liquid; Other Solid

Physikochemische Eigenschaften

Schmelzpunkt
32 · 32-34 °C (lit.)
Siedepunkt
402.85 °C · 402.85°C (rough estimate)
Dichte
0.8 g/mL · 0.8 g/mL at 25 °C (lit.)
Dampfdruck
0.001 Pa · 0.001Pa at 25℃
Brechungsindex
1.5344 · 1.5344 (estimate)
Flammpunkt
230 °F · >230 °F

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 5 Einträge

This chemical does not meet GHS hazard criteria for 0.9% (3 of 339) of reports.

Warning

H315 (99.1%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P333+P317, P337+P317, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 339 reports by companies from 21 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Regulatory Information · 4 Einträge

Chemical: 2-Propenoic acid, octadecyl ester

2-Propenoic acid, octadecyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 2-Propenoic acid, octadecyl ester are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 08-03-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/14496

2-Propenoic acid, octadecyl ester: Does not have an individual approval but may be used under an appropriate group standard

Hazard Classes and CategoriesSkin Irrit. 2 (99.1%)

Sicherheitsdaten

wgk
2
tsca
TSCA listed
ridadr
UN 3077 9 / PGIII
hs_code
29161290
risk_code
41-51/53-36/37/38-43-38
hazard_code
Xi,N

Chemie und Industrie

Verwendung und Herstellung

U.S. Production2023: 400,000 - <550,000 lb
Consumer UsesMonomers
Industry UsesIntermediate
General Manufacturing Information · 2 Einträge

Adhesive Manufacturing

2-Propenoic acid, octadecyl ester: ACTIVE

Anwendungen · 2 Einträge

BeschreibungOctadecyl acrylate is a versatile monomer extensively utilized in synthesizing polymer materials. It presents as a colorless and viscoelastic liquid. Its wide-ranging applications encompass coatings, adhesives, sealants, and printing inks, making it an indispensable ingredient in the polymer industry. Notably, Octadecyl acrylate contributes to the production of polymers used in various medical applications and the manufacturing of polyurethane foams. It serves as a valuable model for studying polymerization reactions, offering insights into the properties of polymer materials. During the polymerization process, Octadecyl acrylate undergoes a crucial reaction. This reaction involves the formation of covalent bonds between the monomer molecules. Precisely, addition polymerization occurs, where a monomer molecule adds to a double bond between two other monomer molecules, establishing the covalent bonds that create the polymer material.

VerwendenOctadecyl Acrylate is a reagent used in the synthesis of comb-like polymers which are incorporated into waterborne latexes improving barrier properties.

Anbieter50 Anbieter

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