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Acrylic Acid → Ethylacrylate acrylic acid acrylonitrile

HRID 1089092
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HRID 1089092 반응식
[C:1]([O:5][CH2:6][CH3:7])(=[O:4])[CH:2]=[CH2:3].[C:8](#[N:11])[CH:9]=[CH2:10].[C:12]([OH:16])(=[O:15])[CH:13]=[CH2:14].C(S)CCCCCCCCCCC.C(OOCCCCCCCCCCCC)CCCCCCCCCCC.C(OOC(=O)C1C=CC=CC=1)CCC>C1(C)C(C)=CC=CC=1>[CH2:6]([O:5][C:1](=[O:4])[CH:2]=[CH2:3])[CH3:7].[C:12]([OH:16])(=[O:15])[CH:13]=[CH2:14].[C:8](#[N:11])[CH:9]=[CH2:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 6581Acrylic AcidHCID 7855AcrylonitrileHCID 81951-DodecanethiolHCID 8821Ethyl AcrylateHCID 76169Lauryl peroxideHCID 83282Butyl perbenzoate

생성물 1

HCID 168852Ethylacrylate acrylic acid acrylonitrile

시약·촉매·용매 1

HCID 7237O-Xylene용매2회

실험 절차

this polymer material was produced by adding to 320 g xylene at 100° C. the monomer solution and a catalyst solution over a period of 3 hours. The monomer solution contained 2.900 g ethyl acrylate, 76 g acrylonitrile, 76 g acrylic acid and 3 g laurylmercaptan. The catalyst solution contained 26 g laurylperoxide and 7 g butylperbenzoate in 273 g of xylene. The material was highly viscous with comonomer proportions of 95:2.5:2.5.

후처리

  1. customthis polymer material was produced

출처 및 근거

ORD 기록
ord-3302c6cf61fb48c19c71da6e8611e7f0
출처 데이터셋
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04965117

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