GB2447026A - Contact adhesive formulation - Google Patents

Contact adhesive formulation Download PDF

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Publication number
GB2447026A
GB2447026A GB0612614A GB0612614A GB2447026A GB 2447026 A GB2447026 A GB 2447026A GB 0612614 A GB0612614 A GB 0612614A GB 0612614 A GB0612614 A GB 0612614A GB 2447026 A GB2447026 A GB 2447026A
Authority
GB
United Kingdom
Prior art keywords
skin
adhering
contact adhesive
hair
unduly
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.)
Withdrawn
Application number
GB0612614A
Other versions
GB0612614D0 (en
Inventor
Susan Ayton-Moon
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB0612614A priority Critical patent/GB2447026A/en
Publication of GB0612614D0 publication Critical patent/GB0612614D0/en
Publication of GB2447026A publication Critical patent/GB2447026A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J171/00Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
    • C09J171/02Polyalkylene oxides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/12Aerosols; Foams
    • A61K9/122Foams; Dry foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q9/00Preparations for removing hair or for aiding hair removal
    • A61Q9/04Depilatories
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/08Homopolymers or copolymers of acrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J171/00Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
    • C09J171/08Polyethers derived from hydroxy compounds or from their metallic derivatives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/14Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02Polyalkylene oxides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Dispersion Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Birds (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)

Abstract

A formulation for a contact adhesive which is capable of adhering to the hair without unduly adhering to the skin and being suitable for use on the skin and suitable for dispensing from effluent only containers such as aerosol, bag-in-can or pump dispensers and preferably containing predominantly acrylates and or polymer such as polyethylene glycol (PEG) and containing trace elements of one, some or all of the following: Triclosan, di-iso-octyl maleate, di-propylene glycol, ethyl hexanol, phenyl hexyl acetate, octyl propionate, linalyl isobutyrate, ethyl hexyl butyrate. di-octyl ether, diethyl phthalate, phenyl methyl octanal, Galaxolide 1 and parfum, and preservatives such as Lilial, iso-methyl ionone, terpene compounds, butylated hydroxy toluene.

Description

* 2447026 Page 1 of 3 Contact Adhesive Formulation
Description
This invention is a skin-friendly contact adhesive formulation capable of foaming and of being dispensed via an aerosolized or effluent-only container.
The background to this invention lies in the depilatory industry. Hair removal via a tacky wax or sugar based compound has widely been used for centuries. However, the basic nature of the fbnnulation is one of stickiness and it often leaves an unpleasant residue on the skin. This can be removed with solvents but these are drying to the skin. More recently water-soluble waxes have become employed but these are still sticky. Many of the waxes on the market today require heating. None of the waxes on the market today are dispensed by an effluent-only dispenser. More often they are applied via a spatula which is dipped into the wax, or a roller bail. Both methods of application carry contamination back into the container from which the wax is dispensed. This allows for the possibility of cross-infection. None of the waxes are capable of foaming and therefore are inclined to drip. To overcome this the present invention can be dispensed from an effluent-only aerosol container and fbrm a foam mass which is easily manipulated onto the skin. It adheres to the hair without adhering unduly to the skin. It adheres to an adhesive strip which is then removed from the skin along with the unwanted hair-growth.
It is essential that this adhesive is capable of being dispensed by an effluent-only container and that it forms a manageable mass. This mass can either be applied directly to the skin or can be applied via an applicator. It is essential that the adhesive does not set in its container. It is desirable that the adhesive foams when dispensed.
Example: An aerosolized can is filled with the formulation. When dispensed it forms a foam ball which can be applied directly to the skin or via an applicator. It is spread onto areas of unwanted hair-growth. A removal strip is placed firmly in contact with the applied formulation and is removed along with the adhesive and the unwanted hair.

Claims (6)

  1. Page 2 of 3 Claims 1. A formulation for a contact adhesive which is
    capable of adhering to the hair without adhering unduly to the skin and being suitable fbr use on the skin and being dispensed via an effluent-only container.
  2. 2. A formulation according to claim I for a contact adhesive which is capable of adhering to the hair without adhering unduly to the skin and being suitable fbr use on the skin and being dispensed via an effluent-only container preferably such as an aerosolized container.
  3. 3. A formulation according to claim 1 for a contact adhesive which is capable of adhering to the hair without adhering unduly to the skin and being suitable for use on the skin and being dispensed via an effluent-only container such as a bag-in-can container.
  4. 4. A formulation according to claim 1 for a contact adhesive which is capable of adhering to the hair without adhering unduly to the skin and being suitable for use on the skin and being dispensed via an effluent-only container such as a pump-dispenser.
  5. 5.
    A formulation according to claims 1-4 for a contact adhesive which is capable of adhering to the hair without adhering unduly to the skin and being suitable fbr use on the skin preferably containing predominantly ACRYLATES and or COPOLYMER such as Polyethylene Glycol (PEG) and containing trace elements of one, some or all of the following: Triclosan; Di-iso-octyl Maleate; di-propylene glycol; Ethyl hexanol; Phenyl hexyl acetate, Octyl propionate, Linalyl isobutyrate, Ethyl hexyl Butyrate; di-octyl ether, Diethyl phthalate; Phenyl methyl octanal and Galaxolide 1.
  6. 6. A formulation according to claims 1-5 for a contact adhesive which is capable of adhering to the hair without adhering unduly to the skin and being suitable for use on the skin and preferably containing predominantly ACRYLATES and or COPOLYMER such as Polyethylene Glycol (PEG) and containing trace elements of one, some or all of the following: Triclosan; Di-iso-octyl Maleate; di-propylene glycol; Ethyl hexanol; Phenyl hexyl acetate, Octyl propionate, Linalyt isobutyrate, Ethyl hexyl Butyrate; di-octyl ether; Diethyl phthalate; Phenyl methyl octanal; Galaxolide I and parfiim, and preservatives such as Lilial, iso-methyl ionone, terpene compounds, Butylated hydroxy toluene.
GB0612614A 2006-06-24 2006-06-24 Contact adhesive formulation Withdrawn GB2447026A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB0612614A GB2447026A (en) 2006-06-24 2006-06-24 Contact adhesive formulation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB0612614A GB2447026A (en) 2006-06-24 2006-06-24 Contact adhesive formulation

Publications (2)

Publication Number Publication Date
GB0612614D0 GB0612614D0 (en) 2006-08-02
GB2447026A true GB2447026A (en) 2008-09-03

Family

ID=36803889

Family Applications (1)

Application Number Title Priority Date Filing Date
GB0612614A Withdrawn GB2447026A (en) 2006-06-24 2006-06-24 Contact adhesive formulation

Country Status (1)

Country Link
GB (1) GB2447026A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013181010A3 (en) * 2012-05-30 2014-03-20 The Procter & Gamble Company Cosmetic products for reducing hair appearance
US9216304B2 (en) 2010-03-26 2015-12-22 The Gillette Company Method of depilation and depilatory kit

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9216304B2 (en) 2010-03-26 2015-12-22 The Gillette Company Method of depilation and depilatory kit
WO2013181010A3 (en) * 2012-05-30 2014-03-20 The Procter & Gamble Company Cosmetic products for reducing hair appearance
CN104470496A (en) * 2012-05-30 2015-03-25 宝洁公司 Cosmetic products for reducing hair appearance

Also Published As

Publication number Publication date
GB0612614D0 (en) 2006-08-02

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WAP Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1)