Dodecylacrylat
Lauryl acrylate
Grundinformationen
- CAS
2156-97-0- Standard-SMILES
C=CC(=O)OCCCCCCCCCCCC- InChIKey
PBOSTUDLECTMNL-UHFFFAOYSA-N- Summenformel
- C15H28O2
- Durchschnittliche Molmasse
- 240,38 g/mol
- Monoisotopische Masse
- 240,20893013
Überblick
Lauryl acrylate is an acrylate ester obtained by the formal condensation of the hydroxy group of dodecan-1-ol with the carboxy group of acrylic acid. It has a role as a pheromone and an animal metabolite. It is functionally related to an acrylic acid and a dodecan-1-ol.
Namen und Bezeichner
- Bevorzugter Name
- Lauryl acrylate
- IUPAC
- dodecyl prop-2-enoate
- Lokaler Name
- Dodecylacrylat
- Englischer Name
- Dodecyl acrylate
- Summenformel
- C15H28O2
- Molmasse
- 240.38
Namen und Synonyme
Dodecyl acrylateLauryl acrylatedodecyl prop-2-enoate2-Propenoic acid, dodecyl esterAcrylic Acid Lauryl EsterAcrylic Acid Dodecyl Esterdodecyl propenoate90IK36WGVRAgeflex FA-12EINECS 218-463-4NSC-24177LIGHT ACRYLATE L-A
Weitere Namen anzeigen
LAMonomerSR-335218-463-4L-61018 LADodecylacrylatF6-BISPHENOL A
UNII-90IK36WGVRPHOTOMER 4812N-Lauryl acrylate (monomer)2-propenoic acid dodecyl esterAI3-03198DTXSID7022178CHEBI:1919512-Propenoic acid, n-dodecyl ester
Datenbank-Bezeichner
- CAS
2156-97-0- PubChem CID
- 75084
- DTXSID
DTXSID7022178- ChEBI
CHEBI:191951- UNII
- 90IK36WGVR
- EC Number
- 218-463-4
- Nikkaji
- J107.540C
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 6,2
- Polarare Oberfläche (TPSA)
- 26,3 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 13
- Schwere Atome
- 17
- Formalladung
- 0
- Komplexität
- 187
Experimentelle und physikochemische Eigenschaften
SpringerMaterials PropertiesBoiling point
Physical DescriptionCBI; Liquid
Physikochemische Eigenschaften
- Schmelzpunkt
- 4 °C · 4 °C
- Siedepunkt
- 120 °C/0.8 · 120 °C/0.8 mmHg
- Dichte
- 0.88 · 0.88
- Dampfdruck
- 0.274 Pa · 0.274Pa at 25℃
- Brechungsindex
- 1.44 · 1.44
- Flammpunkt
- 145 °C · 145 °C
- storage temp.
- Sealed in dry,Room Temperature
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- Aggregatzustand
- clear liquid
- Farbe
- Colorless to Almost colorless
- Wichte
- 0.87 · 0.870.884
- Wasserlöslichkeit
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 3.1% (30 of 956) of reports.
Warning
H315 (96.9%): 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 956 reports by companies from 18 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: 2-Propenoic acid, dodecyl ester
2-Propenoic acid, dodecyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 2-Propenoic acid, dodecyl 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)
REACH registered substance: Dodecyl acrylate (EC: 218-463-4)
2-Propenoic acid, dodecyl ester: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and CategoriesSkin Irrit. 2 (96.9%)
Sicherheitsdaten
- wgk
- 2
- tsca
- TSCA listed
- ridadr
- UN 3082 9/PG 3
- hs_code
- 2916129000
- risk_code
- 36/37/38-51/53
- hazard_code
- Xi,N
Chemie und Industrie
Verwendung und Herstellung
U.S. Production2023: 75,000 - <100,000 lb
Consumer UsesMonomers
Industry UsesMonomers
General Manufacturing Information
Adhesive Manufacturing
2-Propenoic acid, dodecyl ester: ACTIVE
Anwendungen
VerwendenLauryl acrylate can undergo atom transfer radical polymerization (ATRP) to form its polymer. Lauryl acrylate may undergo photoinitiated polymerization in the presence of N-acetyl-4-nitro-1-naphthylamine (ANNA) and N,N-dimethylaniline (DMA).
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