999-21-3C=CCOC(=O)/C=C\C(=O)OCC=CZPOLOEWJWXZUSP-WAYWQWQTSA-NSee also: 2-Butenedioic acid, (Z)-, di-2-propenyl ester (annotation moved to).
999-21-3安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Danger
H301 (90%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 90 reports by companies from 14 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
2-Butenedioic acid (2Z)-, 1,4-di-2-propen-1-yl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 2-Butenedioic acid (2Z)-, 1,4-di-2-propen-1-yl 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: 16-12-2020 https://echa.europa.eu/registration-dossier/-/registered-dossier/23360
2-Butenedioic acid (2Z)-, di-2-propenyl ester: Does not have an individual approval but may be used under an appropriate group standard
All Other Basic Organic Chemical Manufacturing
2-Butenedioic acid (2Z)-, 1,4-di-2-propen-1-yl ester: ACTIVE
使用Diallyl maleate has potential applications in polyester resins, adhesives, and ion exchange resins. When used at low levels, Diallyl Maleate is an effective agent for the promotion of branching in emulsion polymers.
製造方法Diallyl maleate is obtained by the sulfuric acid-catalyzed esterification of maleic anhydride with propyl alcohol.
読み込み中…
DTXSID3044752CHEMBL3186659化学的特性colorless liquid with a pungent odor.