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HRID 1158183作成日:2026年10月27日

Formaldehyde → Melamine formaldehyde

https://huagongshe.com/reaction/1158183

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物MelamineHCID 7955—
反応物Sodium HydroxideHCID 14798—
反応物Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one, 2'-chloro-6'-(diethylamino)-HCID 117320—
溶媒WaterHCID 962—
生成物Melamine formaldehydeHCID 93374—

反応条件

温度60 °C

反応手順

A solution prepared by dissolving 2.5 parts by weight of 3-diethylamino-7-chlorofluoran in 80 parts by weight of NISSEKI HISOL N-296 (an oil, a trade name, mfd. by Nippon Sekiyu Kagaku K.K.) was emulsified in 100 parts by weight of a 5% aqueous solution of pH 4.0 prepared by dissolving a styrene-maleic anhydride copolymer together with a small amount of sodium hydroxide. On the other hand, when a mixture of 10 parts by weight of melamine, 25 parts by weight of a 37% aqueous formaldehyde solution and 65 parts by weight of water was adjusted to pH 9.0 with sodium hydroxide and heated at 60° C., the mixture became transparent after 15 minutes and a melamine-formaldehyde precondensate was obtained. The precondensate was added to the emulsion obtained above, and the resulting mixture was continuously stirred for 4 hours while maintaining the mixture at 60° C., and then was cooled to room temperature. The solid content of the resulting microcapsule dispersion was 45%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07807738B2
出典データセットuspto-grants-2010_10
ORD IDord-d70a22e89aca47e3bd3315e5a4277552
出典メモuspto-grants-2010_10