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
Weitere Namen anzeigen
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
- Formalladung
- 0
- Komplexität
- 261
Experimentelle und physikochemische Eigenschaften
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
- storage temp.
- 2 · 2-8°C, stored under nitrogen
- Löslichkeit
- Insoluble in water
- Aggregatzustand
- powder to lump to clear liquid
- Farbe
- White or Colorless to Almost white or Almost colorless
- Wasserlöslichkeit
- 260.9 ng/L · 260.9ng/L at 25℃
- InChI
- 1S/C21H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23-21(22)4-2/h4H,2-3,5-20H2,1H3
- InChIKey
- FSAJWMJJORKPKS-UHFFFAOYSA-N
- SMILES
- CCCCCCCCCCCCCCCCCCOC(=O)C=C
- LogP
- 9.08 at · 9.08 at 25℃
- CAS Datenbank
- 4813 · 4813-57-4(CAS DataBase Reference)
- NIST chemische Informationen
- Octadecyl acrylate(4813-57-4)
- EPA chemische Informationen
- Stearyl acrylate (4813-57-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
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
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
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
- safety_code
- 26-39-61-36/37/39
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Aquatic Chronic 2Eye Irrit. 2Skin Irrit. 2STOT SE 3
Chemie und Industrie
Verwendung und Herstellung
General Manufacturing Information
Adhesive Manufacturing
2-Propenoic acid, octadecyl ester: ACTIVE
Anwendungen
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.
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