WO1998024409A1 - Schäumende körperreinigungsmittel - Google Patents
Schäumende körperreinigungsmittel Download PDFInfo
- Publication number
- WO1998024409A1 WO1998024409A1 PCT/EP1997/006556 EP9706556W WO9824409A1 WO 1998024409 A1 WO1998024409 A1 WO 1998024409A1 EP 9706556 W EP9706556 W EP 9706556W WO 9824409 A1 WO9824409 A1 WO 9824409A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- surfactant
- atoms
- formula
- foaming
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- 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
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
-
- 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
- A61K8/60—Sugars; Derivatives thereof
- A61K8/604—Alkylpolyglycosides; Derivatives thereof, e.g. esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/596—Mixtures of surface active compounds
Definitions
- the invention relates to foaming body cleansing agents in the form of a liquid surfactant composition based on a combination of strongly foaming anionic surfactants and foam-reinforcing alkyl (poly) glycosides, which, in order to further improve the foam properties, in particular the fine bubbles and durability (creaminess) of the foam, are a combination of a zwitterionic surfactant and an ampholytic surfactant.
- Liquid personal cleansing agents such as those e.g. as liquid soaps, shampoos, shower bath preparations and bubble bath additives are not only good cleaners, they should also be well tolerated by the skin and mucous membranes and should not lead to excessive degreasing or dry skin even with frequent use.
- the consumer also assesses the properties of use according to the amount and quality of the foam that forms during use. In particular, rapid foaming to form fine-bubble and stable foam is desired, and these properties of the foam are usually also described as the creaminess of the foam.
- the body cleansers themselves should also be characterized by a certain thick liquid so that they can be applied to the hand, for example, and not before they are used can be spread on the body surface or on the head, run between the fingers.
- an aqueous detergent composition which contains alkyl sulfate surfactants, alkyl ether sulfate surfactants, alkyl (oligo) glucosides and amphoteric or zwitterionic surfactants.
- the foam properties in particular the fine bubbles and durability of the foam, can be further increased if a combination of a zwitterionic and an ampholytic surfactant is used instead of a betaine or amphoteric surfactant.
- the invention therefore relates to aqueous personal cleansing compositions containing high-foam, skin-compatible anionic surfactants (A) and alkyl (oligo) glycosides (B), which are characterized in that they are a combination to further improve the foam properties and viscosity from a zwitterionic surfactant (C) of the formula I.
- A skin-compatible anionic surfactants
- B alkyl glycosides
- C zwitterionic surfactant
- anionic surfactants A large number of foam-rich, skin-compatible anionic surfactants (A) are known to the person skilled in the art from relevant manuals and are commercially available. These are, in particular, alkyl sulfates in the form of their ammonium or alkanolammonium salts, alkyl ether sulfates, alkyl ether carboxylates, acyl isethionates, acyl sarcosinates, acyl taurines with linear alkyl or acyl groups with 12-18 C atoms and in the form of their alkali metal or ammonium salts.
- the anionic surfactants (A) can be present in the compositions according to the invention in an amount of 3 to 30% by weight.
- alkyl ether sulfates are particularly preferred as anionic surfactants; it is therefore preferred as the anionic surfactant at least one alkyl ether sulfate surfactant of the formula III R 6 O (C 2 H 4 O) m - SO 3 (" ⁇ M (+) (III)
- R is an alkyl or alkenyl group with 12-18 C atoms
- m 1-4
- M (+) is an alkali, magnesium, ammonium or alkanolammonium ion, in an amount of at least 5% by weight of the entire composition included.
- Alkyl (oligo) glycosides (B) have long been known surface-active substances which can be prepared from sugars and aliphatic, primary alcohols with 8-22 C atoms with acetalization.
- Preferred sugar components (glycoses) are glucose, but also fructose, mannose, galactose, talose, gulose, allose, idose, arabinose, xylose, lyxose, ribose and mixtures thereof.
- Preferred because of the easy availability and the good application properties are the acetalization products of glucose with fatty alcohols, which e.g. are available from natural oils and fats by known methods.
- both monoglycosides and oligoglycosides in which a sugar residue is glycosidically bonded to the fatty alcohol are suitable. Mixtures of mono- and oligoglucosides are usually present in the commercial products. ⁇
- Preferred alkyl (oligo) glycosides (B) are those of the formula R (G) x , in which R is a linear alkyl group having 8-16 carbon atoms and (G) x is an (oligo) glucoside residue with an average degree of oligomerization x is from 1 to 2.
- Zwitterionic surfactants (C) of the formula I have also been known for a long time and a large number are commercially available. The best known and most widespread group of these surfactants is that of betaine surfactants where R 2 and R 3 are methyl groups. A further distinction is made between the alkyl betaines in which R 1 is an alkyl or alkylene group and the amide betaines in which R 1 is a group R 5 CONH- (CH 2 ) n -.
- a cocoamidopropyl betaine of formula I in which R 1 is a radical R 5 CONH (CH 2) 3 -, where R 5 CO from a C I2 - is derived C 18 -Kokos- or palm kernel fatty acid, and R 2 and R 3 are methyl groups.
- R 1 is a radical R 5 CONH (CH 2) 3 -, where R 5 CO from a C I2 - is derived C 18 -Kokos- or palm kernel fatty acid, and R 2 and R 3 are methyl groups.
- R 1 is a radical R 5 CONH (CH 2) 3 -, where R 5 CO from a C I2 - is derived C 18 -Kokos- or palm kernel fatty acid, and R 2 and R 3 are methyl groups.
- R 5 CO from a C I2 - is derived C 18 -Kokos- or palm kernel fatty acid
- R 2 and R 3 are methyl groups.
- Amphoteric surfactants (D) of the formula II are also known and commercially available surfactants. They have the property of reacting in acidic solution by protonation on the tertiary nitrogen atom like cationic surfactants and in the alkaline range by salt formation on the carboxyl group like anionic surfactants.
- a particularly suitable ampholytic surfactant (D) is a cocoamphoglycinate of the formula II in which R 1 is a radical R 5 CONH (CH 2 ) 2 -, in which R 5 CO is derived from a Cj 2 -C 18 coconut oil or palm kernel oil fatty acid and R is a hydroxyethyl group.
- R 1 is a radical R 5 CONH (CH 2 ) 2 -, in which R 5 CO is derived from a Cj 2 -C 18 coconut oil or palm kernel oil fatty acid and R is a hydroxyethyl group.
- R 5 CO is derived from a Cj 2 -C 18 coconut oil or palm kernel oil
- aqueous preparations according to the invention can also contain further surfactants and additives. Such additional substances should not make up more than component (A) in their total amount.
- Suitable further additives are, for example, nonionic surfactants, water-soluble polymers, for example cationic polymeric finishing agents, pearlescent substances, dyes, fragrances and suitable emulsifiers, water-soluble polyols such as glycerol, sorbitol, Propylene glycol or polyethylene glycol, electrolyte salts, pH adjusters and cosmetic or dermatological agents.
- nonionic surfactants for example, nonionic surfactants, water-soluble polymers, for example cationic polymeric finishing agents, pearlescent substances, dyes, fragrances and suitable emulsifiers, water-soluble polyols such as glycerol, sorbitol, Propylene glycol or polyethylene glycol, electrolyte salts, pH adjusters and cosmetic or dermatological agents.
- the viscosity of personal cleansing agents according to the invention can still be unsatisfactory. It is a particular advantage of the preparations according to the invention that in such cases the viscosity can easily be increased by adding water-soluble inorganic electrolyte salts.
- Suitable inorganic electrolyte salts are all water-soluble alkali, ammonium and alkaline earth salts, e.g. the fluorides, chlorides, bromides, sulfates, phosphates, nitrates and hydrogen carbonates, insofar as they are soluble in water in an amount of at least 1% by weight at 20 ° C.
- Sodium chloride and magnesium chloride are preferably used.
- the personal cleanser compositions according to the invention can be formulated as highly concentrated pastes with a water content of less than 30% by weight H 2 O or as dilute aqueous lotions with less than 5% by weight of the anionic surfactant (A).
- the content of anionic surfactants (A) is preferably in the range from 5 to 20% by weight.
- body cleansing agents according to the invention can be formulated in a viscosity range of approximately 1 to 200 Pas (20 ° C.), which are suitable as shampoos or shower gels.
- Texapon ® N70 '12 / 14 • Coconut fatty alcohol 2 EO adduct sulfate
- R'CO acyl group of C 8 -C lg coconut fatty acid
- R CO acyl group of Cg-Cjg coconut fatty acid
- Euperlan ® PK 810 pearlescent concentrate contains glycol distearate and Texapon N70.
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE59709526T DE59709526D1 (de) | 1996-12-02 | 1997-11-24 | Schäumende körperreinigungsmittel |
CA002273340A CA2273340A1 (en) | 1996-12-02 | 1997-11-24 | Foaming body-cleansing agents |
SK730-99A SK282097B6 (sk) | 1996-12-02 | 1997-11-24 | Penivé vodné zmesi telových čistiacich prostriedkov |
AT97951960T ATE234072T1 (de) | 1996-12-02 | 1997-11-24 | Schäumende körperreinigungsmittel |
US09/319,192 US6391834B1 (en) | 1996-12-02 | 1997-11-24 | Foaming body-cleansing agents |
EP97951960A EP0942713B1 (de) | 1996-12-02 | 1997-11-24 | Schäumende körperreinigungsmittel |
NO992630A NO992630L (no) | 1996-12-02 | 1999-06-01 | Skummende kroppsrengj°ringsmiddel |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19649895.3 | 1996-12-02 | ||
DE19649895A DE19649895A1 (de) | 1996-12-02 | 1996-12-02 | Schäumende Körperreinigungsmittel |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998024409A1 true WO1998024409A1 (de) | 1998-06-11 |
Family
ID=7813365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1997/006556 WO1998024409A1 (de) | 1996-12-02 | 1997-11-24 | Schäumende körperreinigungsmittel |
Country Status (12)
Country | Link |
---|---|
US (1) | US6391834B1 (de) |
EP (1) | EP0942713B1 (de) |
CN (1) | CN1239424A (de) |
AT (1) | ATE234072T1 (de) |
CA (1) | CA2273340A1 (de) |
CZ (1) | CZ289737B6 (de) |
DE (2) | DE19649895A1 (de) |
ES (1) | ES2195191T3 (de) |
HU (1) | HUP0000361A3 (de) |
NO (1) | NO992630L (de) |
SK (1) | SK282097B6 (de) |
WO (1) | WO1998024409A1 (de) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002097072A2 (en) * | 2001-05-30 | 2002-12-05 | Saechsisches Serumwerk Dresden Branch Of Smithkline Beecham Pharma Gmbh & Co. Kg | Influenza vaccine composition |
WO2004054522A2 (de) * | 2002-12-16 | 2004-07-01 | Henkel Kommanditgesellschaft Auf Aktien | Milde tensidzusammensetzungen |
FR2956975A1 (fr) * | 2010-03-03 | 2011-09-09 | Rhodia Operations | Nouvel agent pour ameliorer le depot d'huile sur les cheveux |
WO2017194339A1 (de) | 2016-05-10 | 2017-11-16 | Basf Se | Mikroemulsionskonzentrate mit amphoteren tensiden |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19957739A1 (de) * | 1999-12-01 | 2001-06-28 | Henkel Ecolab Gmbh & Co Ohg | Handwaschlotion für wiederbefüllbare Schaumerzeugungsvorrichtung |
FR2811570B1 (fr) * | 2000-07-12 | 2002-09-06 | Oreal | Composition de nettoyage moussante sous la forme d'un gel transparent |
US8361292B2 (en) | 2007-04-27 | 2013-01-29 | Arkray, Inc. | Method for analyzing hemoglobin by capillary electrophoresis and additive used therein |
DE102007028509A1 (de) * | 2007-06-18 | 2008-12-24 | Henkel Ag & Co. Kgaa | Flüssiges, hochschäumendes Wasch- oder Reinigungsmittel mit stabiler Viskosität |
CN101808613B (zh) * | 2007-06-19 | 2015-05-06 | 考格尼斯知识产权管理有限责任公司 | 具有改进的护理功效的洗发水组合物 |
US8846063B2 (en) * | 2008-12-16 | 2014-09-30 | Kimberly-Clark Worldwide, Inc. | Personal care composition containing a volatile and a terpene alcohol |
DE102010022062A1 (de) * | 2010-05-31 | 2011-12-01 | Beiersdorf Ag | Kosmetisches Körperreinigungsmittel mit nicht spürbarem Fehlen von alkoxylierten Tensiden |
FR2976483B1 (fr) * | 2011-06-17 | 2013-07-26 | Oreal | Composition cosmetique comprenant un tensioactif anionique, un tensioactif non ionique ou amphotere et un alcool gras solide et procede de traitement cosmetique |
US9138429B2 (en) | 2011-06-23 | 2015-09-22 | The Procter & Gamble Company | Process of forming crystals for use in a personal care composition |
US20220062136A1 (en) * | 2020-08-31 | 2022-03-03 | L'oreal | Compositions and methods for cleansing keratin materials |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4131992A1 (de) * | 1991-09-26 | 1993-04-01 | Wella Ag | Fixiermittel und verfahren zur dauerhaften haarverformung |
DE4234487A1 (de) * | 1992-10-14 | 1994-04-21 | Henkel Kgaa | Wäßrige Detergensgemische |
DE4301820A1 (de) * | 1993-01-23 | 1994-07-28 | Henkel Kgaa | Schäumende Emulsionen |
DE4435387A1 (de) * | 1994-10-04 | 1996-04-11 | Henkel Kgaa | Pumpfähige wäßrige Tensidkonzentrate |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6087320A (en) * | 1989-09-14 | 2000-07-11 | Henkel Corp. | Viscosity-adjusted surfactant concentrate compositions |
US5653970A (en) * | 1994-12-08 | 1997-08-05 | Lever Brothers Company, Division Of Conopco, Inc. | Personal product compositions comprising heteroatom containing alkyl aldonamide compounds |
US5858957A (en) * | 1995-01-26 | 1999-01-12 | The Procter & Gamble Company | Process for the manufacture of granular detergent compositions comprising nonionic surfactant |
US5981452A (en) * | 1995-12-04 | 1999-11-09 | Henkel Kommanditgesellschaft Auf Aktien | Syndet soaps comprising alkyl and/or alkenyl oligoglycosides |
-
1996
- 1996-12-02 DE DE19649895A patent/DE19649895A1/de not_active Withdrawn
-
1997
- 1997-11-24 CA CA002273340A patent/CA2273340A1/en not_active Abandoned
- 1997-11-24 DE DE59709526T patent/DE59709526D1/de not_active Expired - Fee Related
- 1997-11-24 AT AT97951960T patent/ATE234072T1/de not_active IP Right Cessation
- 1997-11-24 HU HU0000361A patent/HUP0000361A3/hu unknown
- 1997-11-24 CZ CZ19991950A patent/CZ289737B6/cs not_active IP Right Cessation
- 1997-11-24 WO PCT/EP1997/006556 patent/WO1998024409A1/de active IP Right Grant
- 1997-11-24 CN CN97180195A patent/CN1239424A/zh active Pending
- 1997-11-24 US US09/319,192 patent/US6391834B1/en not_active Expired - Fee Related
- 1997-11-24 EP EP97951960A patent/EP0942713B1/de not_active Expired - Lifetime
- 1997-11-24 SK SK730-99A patent/SK282097B6/sk unknown
- 1997-11-24 ES ES97951960T patent/ES2195191T3/es not_active Expired - Lifetime
-
1999
- 1999-06-01 NO NO992630A patent/NO992630L/no not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4131992A1 (de) * | 1991-09-26 | 1993-04-01 | Wella Ag | Fixiermittel und verfahren zur dauerhaften haarverformung |
DE4234487A1 (de) * | 1992-10-14 | 1994-04-21 | Henkel Kgaa | Wäßrige Detergensgemische |
DE4301820A1 (de) * | 1993-01-23 | 1994-07-28 | Henkel Kgaa | Schäumende Emulsionen |
DE4435387A1 (de) * | 1994-10-04 | 1996-04-11 | Henkel Kgaa | Pumpfähige wäßrige Tensidkonzentrate |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002097072A2 (en) * | 2001-05-30 | 2002-12-05 | Saechsisches Serumwerk Dresden Branch Of Smithkline Beecham Pharma Gmbh & Co. Kg | Influenza vaccine composition |
WO2002097072A3 (en) * | 2001-05-30 | 2003-04-24 | Saechsisches Serumwerk | Influenza vaccine composition |
US7316813B2 (en) | 2001-05-30 | 2008-01-08 | Saechsisches Serumwerk Dresden Branch Of Smithkline Beecham Pharma Gmbh & Co Kg | Influenza vaccine composition |
EP2039761A1 (de) * | 2001-05-30 | 2009-03-25 | Saechsisches Serumwerk Dresden | Grippe-Impstoffzusammensetzung |
WO2004054522A2 (de) * | 2002-12-16 | 2004-07-01 | Henkel Kommanditgesellschaft Auf Aktien | Milde tensidzusammensetzungen |
WO2004054522A3 (de) * | 2002-12-16 | 2004-09-10 | Henkel Kgaa | Milde tensidzusammensetzungen |
FR2956975A1 (fr) * | 2010-03-03 | 2011-09-09 | Rhodia Operations | Nouvel agent pour ameliorer le depot d'huile sur les cheveux |
WO2011107713A2 (fr) * | 2010-03-03 | 2011-09-09 | Rhodia Operations | Nouvel agent pour améliorer le dépôt d'huile sur les cheveux |
WO2011107713A3 (fr) * | 2010-03-03 | 2012-10-26 | Rhodia Operations | Nouvel agent pour améliorer le dépôt d'huile sur les cheveux |
CN102821745A (zh) * | 2010-03-03 | 2012-12-12 | 罗地亚管理公司 | 改善油在头发上的沉积的新试剂 |
WO2017194339A1 (de) | 2016-05-10 | 2017-11-16 | Basf Se | Mikroemulsionskonzentrate mit amphoteren tensiden |
Also Published As
Publication number | Publication date |
---|---|
ES2195191T3 (es) | 2003-12-01 |
CZ195099A3 (cs) | 1999-10-13 |
HUP0000361A2 (en) | 2000-07-28 |
US6391834B1 (en) | 2002-05-21 |
SK73099A3 (en) | 2000-02-14 |
SK282097B6 (sk) | 2001-11-06 |
NO992630D0 (no) | 1999-06-01 |
DE19649895A1 (de) | 1998-06-04 |
DE59709526D1 (de) | 2003-04-17 |
EP0942713A1 (de) | 1999-09-22 |
ATE234072T1 (de) | 2003-03-15 |
EP0942713B1 (de) | 2003-03-12 |
CN1239424A (zh) | 1999-12-22 |
HUP0000361A3 (en) | 2002-11-28 |
CA2273340A1 (en) | 1998-06-11 |
NO992630L (no) | 1999-06-01 |
US20020032133A1 (en) | 2002-03-14 |
CZ289737B6 (cs) | 2002-03-13 |
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