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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1757374생성일: 2026년 10월 25일

4-((4-Isothiocyanatophenyl)azo)-N,N-dimethylaniline → Erythrosine

https://huagongshe.com/reaction/1757374

반응식

참여 물질

역할이름HCID투입량
반응물4-((4-Isothiocyanatophenyl)azo)-N,N-dimethylanilineHCID 82084—
반응물Erythrosine isothiocyanateHCID 188262—
용매DimethylformamideHCID 6228—
용매Sodium BicarbonateHCID 516892—
생성물ErythrosineHCID 3259—

반응 단계

Antibody (2 mg) was dissolved in 2 ml of 1% NaHCO3, pH 8.6, and a 20-μl aliquot of a solution of 1 mg/ml 4-dimethylaminoazobenzene-4'-isothiocyanate in dimethylformamide (DMF) added. The mixture was stirred overnight, then desalted on a Sephadex G-25(coarse) column (1×30 cm). The ultraviolet and visible spectrum of the conjugate was compared to that of DAB and antibody alone, to determinethe degree of substitution. The erythrosin-antibody conjugate was prepared the same way, except the concentration of the erythrosin-isothiocyanate inDMF was 2.5 mg/ml.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05445972
출처 데이터셋uspto-grants-1995_08
ORD IDord-bce9d857e0eb4c0a94ae0512de36b0d3
출처 메모uspto-grants-1995_08