Lauryl acrylate
2156-97-0C=CC(=O)OCCCCCCCCCCCCPBOSTUDLECTMNL-UHFFFAOYSA-NLauryl 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.
2156-97-0DTXSID7022178CHEBI:191951안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
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.
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
Adhesive Manufacturing
2-Propenoic acid, dodecyl ester: ACTIVE
용도Lauryl 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).
일반 설명Lauryl acrylate monomers are extremely hydrophobic in nature.
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Colorless liquid