DE2248290A1 - HAIRCARE PRODUCTS AND METHOD OF MANUFACTURING THESS - Google Patents

HAIRCARE PRODUCTS AND METHOD OF MANUFACTURING THESS

Info

Publication number
DE2248290A1
DE2248290A1 DE19722248290 DE2248290A DE2248290A1 DE 2248290 A1 DE2248290 A1 DE 2248290A1 DE 19722248290 DE19722248290 DE 19722248290 DE 2248290 A DE2248290 A DE 2248290A DE 2248290 A1 DE2248290 A1 DE 2248290A1
Authority
DE
Germany
Prior art keywords
monostearate
urea
isopropyl myristate
nicotinic acid
possibly
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.)
Pending
Application number
DE19722248290
Other languages
German (de)
Inventor
Eino Marttinen
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.)
INDAL Oy
Original Assignee
INDAL Oy
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 INDAL Oy filed Critical INDAL Oy
Publication of DE2248290A1 publication Critical patent/DE2248290A1/en
Pending legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q7/00—Preparations for affecting hair growth
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36—Carboxylic acids; Salts or anhydrides thereof
    • A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42—Amides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67—Vitamins
    • A61K8/673—Vitamin B group
    • A61K8/675—Vitamin B3 or vitamin B3 active, e.g. nicotinamide, nicotinic acid, nicotinyl aldehyde

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

PATENTANWALTSBORO HOMSEN - TlEDTKE - BüHLSNGPATENT AGENT BORO HOMSEN - TlEDTKE - BüHLSNG

TEL. (0811) 53 0211 TELEX: 5-24 303 topat 22 A 8290TEL. (0811) 53 0211 TELEX: 5-24 303 topat 22 A 8290

53 021253 0212

PATENTANWÄLTEPATENT LAWYERS

München: Frankfurt/M.:Munich: Frankfurt / M .:

Dipl.-Chem.Dr.D.Thomsen Dipl.-Ing. W. WtelnkauffDipl.-Chem. Dr. D. Thomsen Dipl.-Ing. W. Wtelnkauff

Dipl.-Ing. H. Tiedtke (fuchshohl 71)Dipl.-Ing. H. Tiedtke (fuchshohl 71)

Dipl.-Chem. G. Bühling Dipl.-Ing. R. Kinne Dipl.-Chem. Dr. U. EggersDipl.-Chem. G. Bühling Dipl.-Ing. R. Kinne Dipl.-Chem. Dr. U. Eggers

8000 München 28000 Munich 2

Kalser-Ludwlg-Platz 6 2. Oktober 1972Kalser-Ludwlg-Platz 6 October 2nd, 1972

Indal Oy
Helsinki (Finnland)Indal Oy
Helsinki (Finland)

Haarpflegemittel sowie Verfahren zur Herstellung desselbenHair care products and processes for their manufacture

Die vorliegende Erfindung betrifft ein Haarpflegemittel, welches eine günstige Wirkung auf das Wachstum des Haars ausübt und -das keine schädlichen Nebenwirkungen hat.The present invention relates to a hair care product which has a beneficial effect on hair growth and that has no harmful side effects.

Das Mittel nach der vorliegenden Erfindung ist somit dadurch gekennzeichnet, dass das Mittel in Äthanol gelöste Nikotinsäure und möglicherweise eine oder mehrere aromatische Carbonsäuren, Harnstoff, Polyäthylensorbitan-Monopalmitat oder -Monostearat sowie Isopropy-1-myristat enthält. Günstige aromatische Carbonsäuren sind Salicyl- oder Benzoesäure, die also einzeln oder zusammen verwendet werden können.The agent according to the present invention is thus characterized that the agent is nicotinic acid dissolved in ethanol and possibly one or more aromatic carboxylic acids, urea, Polyethylene sorbitan monopalmitate or monostearate and isopropy-1-myristate contains. Favorable aromatic carboxylic acids are salicylic or benzoic acids, which are used individually or together can.

In einem Mittel nach der Erfindung kann man beispielsweise die folgenden Stoffmengen verwenden: 100 ml des Mittels enthalten 1 g Nikotinsäure und möglicherweise 0,1 g Salicyl- und/oder Benzoesäure ; in 10 ml Äthanol gelöst, 2 g Harnstoff, 60 ml Polyoxyäthylensorbitan-Monopalmitat oder -Monostearat, während der Rest aus Isopropylmyristat besteht.In an agent according to the invention, for example, the following can be used Use amounts of substance: 100 ml of the product contains 1 g of nicotinic acid and possibly 0.1 g of salicylic and / or benzoic acid; Dissolved in 10 ml of ethanol, 2 g of urea, 60 ml of polyoxyethylene sorbitan monopalmitate or monostearate, while the remainder is isopropyl myristate.

Die vorliegende Erfindung bezieht sich auch auf ein Verfahren zum Herstellen eines Haarmittels. Dae Verfahren ist dadurch gekennzeichnet,The present invention also relates to a method of making a hair composition. The process is characterized by

309820/1008309820/1008

Mündliche Abreden, Insbetonder· durch Telefon, bedürfen schriftlicher Betätigung PotUcheck (München) Kto. 116974 Drtidnar Bank (München) Kto. 5 569 708Verbal agreements, in particular by telephone, require written confirmation PotUcheck (Munich) Account 116974 Drtidnar Bank (Munich) Account 5 569 708

dass die Salicylsäure zusammen mit der Nikotinsäure in Alkohol unter Erwärmung auf etwa 3O-35°C gelöst wird, der Harnstoff und das Monopalmitat oder Monostearat unter Erwärmung auf etwa 500C gemischt werden, die Mischungen vereinigt werden und das Isopropylmyristat unter Umrühren zugesetzt wird,is achieved that the salicylic acid together with the nicotinic acid in alcohol under heating to about 3O-35 ° C, the urea and the monopalmitate or monostearate under heating are mixed at about 50 0 C, the mixtures are combined and the isopropyl myristate is added under stirring,

Beispielexample

1 g Nikotinsäure wird in 10 ml Äthanol (96prozentig oder absolut) gelöst. Die Auflösung wird durch behutsames Erwärmen auf etwa 3O-35°C auf dem Wasserbad beschleunigt. Alternativ kann man zusätzlich zur Nikotinsäure 0,1 g Salicyl- oder Benzoesäure oder 0,1 g dieser Säuren verwenden. Zu 60 ml Polyoxyäthylensorbinat-Monopalmitat oder -Monostearat werden 2 g Harnstoff zugesetzt. Diese Mischung wird auf dem Wasserbad auf etwa 500C erwärmt. Als zum Verbessern der Konsistenz der Salbe beabsichtigte Substanz wird handelsübliches Polyoxyäthylensorbitan-Monopalmitat ("Tween Ί0") oder Polyoxyäthylensorbitan-Monostearat ("Tween 60") benutzt. Die derart hergestellten beiden Mischungen werden unter Mischen vereinigt und zur Mischung wird zwecks Verbesserung der Löslichkeit des Monopalmitats oder Monostearats Isopropylmyristat in einer Menge von etwa 30 ml zugegeben, wobei die endgültige Menge des hergestellten Präparats 100 ml wird»1 g of nicotinic acid is dissolved in 10 ml of ethanol (96 percent or absolute). The dissolution is accelerated by gently warming to about 30-35 ° C on a water bath. Alternatively, 0.1 g of salicylic or benzoic acid or 0.1 g of these acids can be used in addition to nicotinic acid. 2 g of urea are added to 60 ml of polyoxyethylene sorbinate monopalmitate or monostearate. This mixture is heated to about 50 ° C. on the water bath. Commercially available polyoxyethylene sorbitan monopalmitate ("Tween Ί0") or polyoxyethylene sorbitan monostearate ("Tween 60") is used as the substance intended to improve the consistency of the ointment. The two mixtures prepared in this way are combined with mixing and isopropyl myristate is added to the mixture in an amount of about 30 ml in order to improve the solubility of the monopalmitate or monostearate, the final amount of the preparation produced being 100 ml »

3098 2 0/ IO C) B3098 2 0 / IO C) B.

Claims (3)

PatentansprücheClaims 1. Haarpflegemittel, dadurch gekennzeichnet, dass das Mittel in Äthanol gelöste Nikotinsäure und möglicherweise eine oder mehrere aromatische Carbonsäuren, Harnstoff, Polyoxyäthylensorbitan-Monopalmitat oder -Monostearat sowie Isopropylmyristat enthält,1. Hair care products, characterized in that the means in Nicotinic acid dissolved in ethanol and possibly one or more aromatic carboxylic acids, urea, polyoxyethylene sorbitan monopalmitate or monostearate and isopropyl myristate, 2. Mittel nach Anspruch 1, dadurch gekennzeichnet, dass als aromatische Carbonsäure Salicyl- oder Benzoesäure verwendet wird, ·2. Means according to claim 1, characterized in that as aromatic Carboxylic acid salicylic or benzoic acid is used, 3. Mittel nach Anspruch 1 oder 2, dadurch gekennzeichnet, dass ml des Mittels 1 g Nikotinsäure und möglicherweise 0,1 g Salicyl- und/oder Benzoesäure in 10 ml Äthanol gelöst, 2 g Harnstoff, 60 ml Polyoxyäthylensorbitan-Monopalmitat oder -Monostearat enthalten, während der restliche Teil aus Isopropylmyristat besteht.3. Means according to claim 1 or 2, characterized in that ml of the agent 1 g of nicotinic acid and possibly 0.1 g of salicylic and / or benzoic acid dissolved in 10 ml of ethanol, 2 g of urea, 60 ml Contain polyoxyethylene sorbitan monopalmitate or monostearate, while the remaining part consists of isopropyl myristate. 1J. Verfahren zum Herstellen eines Mittels nach den vorhergehenden Ansprüchen, dadurch gekennzeichnet, dass die Nikotinsäure zusammen möglicherweise mit einer oder mehreren aromatischen Carbonsäuren in Alkohol unter Erwärmung auf etwa 30-35°C gelöst wird, der Harnstoff und das Monopalmitat oder Monostearat unter Erwärmung auf etwa 50-60°C gemischt werden, die Mischungen vereinigt werden und das Isopropylmyristat unter Mischen zugesetzt wird, 1 J. Process for producing an agent according to the preceding claims, characterized in that the nicotinic acid is dissolved together possibly with one or more aromatic carboxylic acids in alcohol with heating to about 30-35 ° C, the urea and the monopalmitate or monostearate with heating mixed to about 50-60 ° C, the mixtures combined and the isopropyl myristate added with mixing, 309820/1008309820/1008
DE19722248290 1971-11-11 1972-10-02 HAIRCARE PRODUCTS AND METHOD OF MANUFACTURING THESS Pending DE2248290A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FI322371 1971-11-11

Publications (1)

Publication Number Publication Date
DE2248290A1 true DE2248290A1 (en) 1973-05-17

Family

ID=8508166

Family Applications (1)

Application Number Title Priority Date Filing Date
DE19722248290 Pending DE2248290A1 (en) 1971-11-11 1972-10-02 HAIRCARE PRODUCTS AND METHOD OF MANUFACTURING THESS

Country Status (7)

Country Link
JP (1) JPS4858149A (en)
CA (1) CA986414A (en)
CH (1) CH566133A5 (en)
DE (1) DE2248290A1 (en)
FR (1) FR2159400B1 (en)
GB (1) GB1354446A (en)
NL (1) NL7214875A (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3514087A1 (en) * 1985-04-18 1986-10-23 Laszlo Dr Med Szekely Hair treatment composition and process for the cosmetic treatment of hair and hair matrix
WO1989005626A1 (en) * 1987-12-24 1989-06-29 Fujisawa Pharmaceutical Co., Ltd. Hair growth promoting agent
GB2235380A (en) * 1989-08-29 1991-03-06 Oswald Morton Anti-dandruff composition
EP0471135B1 (en) * 1990-08-14 1997-06-11 Kenneth M. Hallam Composition for the promotion of hair growth
US5959066A (en) * 1998-04-23 1999-09-28 Hna Holdings, Inc. Polyesters including isosorbide as a comonomer and methods for making same
US5958581A (en) * 1998-04-23 1999-09-28 Hna Holdings, Inc. Polyester film and methods for making same
US6025061A (en) * 1998-04-23 2000-02-15 Hna Holdings, Inc. Sheets formed from polyesters including isosorbide
US6063495A (en) * 1998-04-23 2000-05-16 Hna Holdings, Inc. Polyester fiber and methods for making same
US6140422A (en) * 1998-04-23 2000-10-31 E.I. Dupont De Nemours And Company Polyesters including isosorbide as a comonomer blended with other thermoplastic polymers
US6126992A (en) 1998-04-23 2000-10-03 E.I. Dupont De Nemours And Company Optical articles comprising isosorbide polyesters and method for making same
US7598278B2 (en) 2002-04-11 2009-10-06 L'oreal Administration of pyridinedicarboxylic acid compounds for stimulating or inducing the growth of human keratinous fibers and/or arresting their loss
FR3030248B1 (en) 2014-12-22 2018-03-23 L'oreal PYRIDINE-DICARBOXYLIC ACID DERIVATIVE ASSOCIATION / PARTICULAR ANTIOXIDANT AGENT

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE547445A (en) * 1955-04-29
BE592793A (en) * 1959-07-09

Also Published As

Publication number Publication date
GB1354446A (en) 1974-06-05
FR2159400A1 (en) 1973-06-22
NL7214875A (en) 1973-05-15
FR2159400B1 (en) 1975-03-28
CA986414A (en) 1976-03-30
CH566133A5 (en) 1975-09-15
JPS4858149A (en) 1973-08-15

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