JPS5714652A - Discoloration, color development, or color fading material composed of indoline derivative - Google Patents

Discoloration, color development, or color fading material composed of indoline derivative

Info

Publication number
JPS5714652A
JPS5714652A JP8952480A JP8952480A JPS5714652A JP S5714652 A JPS5714652 A JP S5714652A JP 8952480 A JP8952480 A JP 8952480A JP 8952480 A JP8952480 A JP 8952480A JP S5714652 A JPS5714652 A JP S5714652A
Authority
JP
Japan
Prior art keywords
color
indoline derivative
discoloration
alkyl
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP8952480A
Other languages
Japanese (ja)
Other versions
JPS6361994B2 (en
Inventor
Masaaki Hayamizu
Katsutoshi Mitsumoto
Katsumasa Taniguchi
Kazuteru Ogo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Kanko Shikiso Kenkyusho KK
Original Assignee
Nippon Kanko Shikiso Kenkyusho KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Kanko Shikiso Kenkyusho KK filed Critical Nippon Kanko Shikiso Kenkyusho KK
Priority to JP8952480A priority Critical patent/JPS5714652A/en
Publication of JPS5714652A publication Critical patent/JPS5714652A/en
Publication of JPS6361994B2 publication Critical patent/JPS6361994B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE: To obtain a discoloration, color development or fading material having long life and excellent stability, and capable of discoloring, developing or fading the color by the application of external energy stimmulation such as light, heat, ion, electricity, pressure, etc., by using a specific indoline derivative as a main component.
CONSTITUTION: The objective composition contains, as a main component, an indoline derivative of formula I (R is alkyl or phenyl; R1 and R2 are lower alkyl, hydroxyalkyl, etc.; R3 is H or alkyl; Z is methylene, ethylene, etc.; A is condensation reaction residue of aromatic aldehyde or heterocyclic aldehyde, etc.; n is 2 or 3), e.g. 3,3-dimethyl-5-methylsulfonyl-2- ( p-dimethylaminostyryl ) -indolino [ 2,1-b ] - oxazolo-5-one of formula II. The compound can be reversibly converted e.g. to the indolenium-type ring-opened colored structure (styryl dye) of formula III (X is halogen, acid radical, etc.) and colored or discolored by applying external energy stimmulation such as light, heat, ion, electricity, pressure, radiations, etc.
COPYRIGHT: (C)1982,JPO&Japio
JP8952480A 1980-06-30 1980-06-30 Discoloration, color development, or color fading material composed of indoline derivative Granted JPS5714652A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8952480A JPS5714652A (en) 1980-06-30 1980-06-30 Discoloration, color development, or color fading material composed of indoline derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8952480A JPS5714652A (en) 1980-06-30 1980-06-30 Discoloration, color development, or color fading material composed of indoline derivative

Publications (2)

Publication Number Publication Date
JPS5714652A true JPS5714652A (en) 1982-01-25
JPS6361994B2 JPS6361994B2 (en) 1988-11-30

Family

ID=13973186

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8952480A Granted JPS5714652A (en) 1980-06-30 1980-06-30 Discoloration, color development, or color fading material composed of indoline derivative

Country Status (1)

Country Link
JP (1) JPS5714652A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2888747A1 (en) * 2005-07-22 2007-01-26 Oreal USE FOR THE COLORING OF KERATIN FIBERS OF A COMPOSITION COMPRISING A STYRYLIC OR IMINIC COLORANT
US7527654B2 (en) 2006-10-13 2009-05-05 L'oreal S.A. Dyeing process using a dye of styryl or imine type in combination with a weak acid, and device for implementing the process
FR2930141A1 (en) * 2008-04-16 2009-10-23 Oreal Treatment of keratin fibers, preferably capillaries, comprises applying a washing composition, rinsing, and drying or leaving to dry the fibers, where the fibers have undergone coloring process with styryl or imine compounds

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2888747A1 (en) * 2005-07-22 2007-01-26 Oreal USE FOR THE COLORING OF KERATIN FIBERS OF A COMPOSITION COMPRISING A STYRYLIC OR IMINIC COLORANT
EP1747774A1 (en) * 2005-07-22 2007-01-31 L'Oréal Use of a composition comprising a colouring agent of the styrylic or imino type for dyeing keratinuous fibres
US7399319B2 (en) 2005-07-22 2008-07-15 L'oreal S.A. Dyeing composition comprising a dye chosen from styryl and imine dyes and methods for dyeing keratin fibers
US7527654B2 (en) 2006-10-13 2009-05-05 L'oreal S.A. Dyeing process using a dye of styryl or imine type in combination with a weak acid, and device for implementing the process
FR2930141A1 (en) * 2008-04-16 2009-10-23 Oreal Treatment of keratin fibers, preferably capillaries, comprises applying a washing composition, rinsing, and drying or leaving to dry the fibers, where the fibers have undergone coloring process with styryl or imine compounds
WO2010128214A1 (en) * 2008-04-16 2010-11-11 L´Oreal Treatment of colored fibers by styryl or imine compounds in the presence of organic or inorganic acids and zinc salts

Also Published As

Publication number Publication date
JPS6361994B2 (en) 1988-11-30

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