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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576739Generated: October 26, 2026

Dianisidine → 2-Naphthol

https://huagongshe.com/reaction/1576739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDianisidineHCID 8411—
ReactantSodium HydroxideHCID 14798—
Product2-NaphtholHCID 8663—

Reaction Steps

Silica particles were derivatized with o-dianisidine by Method No. 2. After drying, 1.0 gm of the carrier was diazotized with sodium nitrite. After diazotization the derivative was washed several times with borate (0.03M) buffered saline (0.15M) pH 8.0. The derivative was then reacted with 1.5 ml of T4 antisera (titer 1:10000) at 4°C. with stirring. The pH was maintained between 8.0 - 8.5 with 0.1N NaOH. After 30 minutes the pH stabilized at 8.2 and the reaction was stirred slowly at 4°C. overnight. After this time the composite gave a negative β-napthol test indicating no more remaining functional diazo groups. The preparation was then washed (4X) with phosphate-buffer (0.03M) saline (0.15M) containing 0.1% bovine serum albumin (PBS-BSA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03983000
Source datasetuspto-grants-1976_09
ORD IDord-2178f3db996a407b8d5833f978e270e8
Source noteuspto-grants-1976_09