NO132415B - - Google Patents
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- Publication number
- NO132415B NO132415B NO535/70A NO53570A NO132415B NO 132415 B NO132415 B NO 132415B NO 535/70 A NO535/70 A NO 535/70A NO 53570 A NO53570 A NO 53570A NO 132415 B NO132415 B NO 132415B
- Authority
- NO
- Norway
- Prior art keywords
- weight
- film
- polymer
- water
- active agent
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 claims description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 27
- 239000013543 active substance Substances 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 239000000516 sunscreening agent Substances 0.000 claims description 17
- 230000000475 sunscreen effect Effects 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 9
- 239000002304 perfume Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000000077 insect repellent Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000003974 emollient agent Substances 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 19
- 238000002360 preparation method Methods 0.000 description 19
- 235000019441 ethanol Nutrition 0.000 description 11
- 230000037072 sun protection Effects 0.000 description 11
- 239000002562 thickening agent Substances 0.000 description 8
- 229920000058 polyacrylate Polymers 0.000 description 6
- 229940096529 carboxypolymethylene Drugs 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 210000000245 forearm Anatomy 0.000 description 4
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 4
- 229960001860 salicylate Drugs 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 206010042496 Sunburn Diseases 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- KUYQDJOFVBGZID-UHFFFAOYSA-N n,n-diethyl-2-methylbenzamide Chemical compound CCN(CC)C(=O)C1=CC=CC=C1C KUYQDJOFVBGZID-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- FIWQKJBSPKNFAM-QGAMPUOQSA-N (z)-4-ethoxy-4-oxobut-2-enoic acid;styrene Chemical compound C=CC1=CC=CC=C1.CCOC(=O)\C=C/C(O)=O FIWQKJBSPKNFAM-QGAMPUOQSA-N 0.000 description 1
- GVJRTUUUJYMTNQ-UHFFFAOYSA-N 2-(2,5-dioxofuran-3-yl)acetic acid Chemical compound OC(=O)CC1=CC(=O)OC1=O GVJRTUUUJYMTNQ-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 229940091181 aconitic acid Drugs 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- -1 polysiloxane Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume 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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of 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; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79987369A | 1969-02-17 | 1969-02-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
NO132415B true NO132415B (fr) | 1975-08-04 |
NO132415C NO132415C (fr) | 1975-11-12 |
Family
ID=25176986
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO535/70A NO132415C (fr) | 1969-02-17 | 1970-02-16 |
Country Status (14)
Country | Link |
---|---|
US (1) | US3784488A (fr) |
JP (1) | JPS4924223B1 (fr) |
AT (1) | AT323328B (fr) |
BE (1) | BE746015A (fr) |
CA (1) | CA921629A (fr) |
CH (1) | CH537437A (fr) |
DE (1) | DE2005084C3 (fr) |
DK (1) | DK125956C (fr) |
FR (1) | FR2034760B1 (fr) |
GB (1) | GB1296241A (fr) |
MY (1) | MY7300339A (fr) |
NL (1) | NL7001258A (fr) |
NO (1) | NO132415C (fr) |
SE (1) | SE354783B (fr) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE787932A (fr) * | 1971-09-13 | 1973-02-26 | Bristol Myers Co | Produits tels que des tampons, pour nettoyage ou d'autres usages et compositions liquides pour preparer ces produits |
GB1552942A (en) * | 1975-07-17 | 1979-09-19 | Sumitomo Electric Industries | Process for producing a porous material having a fine pore size |
US4938951A (en) * | 1980-12-30 | 1990-07-03 | Union Carbide Chemicals And Plastics Company Inc. | Potentiation of topical compositions wherein a uniform microdispersion of active agent is formed |
DE3204551A1 (de) * | 1982-02-10 | 1983-08-18 | Boehringer Ingelheim KG, 6507 Ingelheim | Verfahren zur herstellung einer pharmazeutischen zubereitung in form eines polyacrylat-films |
US4455272A (en) * | 1982-03-29 | 1984-06-19 | Standard Oil Company (Indiana) | Method of extruding a polystyrene foam using both a physical blowing agent and water |
US5364628A (en) * | 1985-05-31 | 1994-11-15 | Sandoz Ltd. | Pharmaceutical compositions |
US4663157A (en) * | 1985-02-28 | 1987-05-05 | The Proctor & Gamble Company | Sunscreen compositions |
EP0195575B1 (fr) * | 1985-03-21 | 1989-12-27 | Charles Of The Ritz Group Ltd. | Formule pour rouge à lèvres en bâton et procédé |
US4816256A (en) * | 1986-10-10 | 1989-03-28 | Minnesota Mining And Manufacturing Company | Mosquito repellent compositions |
US5004598A (en) * | 1986-11-10 | 1991-04-02 | The B. F. Goodrich Company | Stable and quick-breaking topical skin compositions |
US4810489A (en) * | 1986-12-04 | 1989-03-07 | Bristol-Myers Company | High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors |
US4897259A (en) * | 1986-12-04 | 1990-01-30 | Bristol-Myers Company | High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors |
JP2563814B2 (ja) * | 1987-11-12 | 1996-12-18 | 日東電工株式会社 | 液状活性物質徐放デバイス |
FR2696902B1 (fr) * | 1992-10-21 | 1995-01-06 | Health Business Dev | Composition antiparasitaire pour application externe. |
FI952065A0 (fi) * | 1995-03-01 | 1995-04-28 | Xyrofin Oy | Foerfarande foer tillvaratagande av en kristalliserbar organisk foerening |
JP3180131B2 (ja) | 1996-03-28 | 2001-06-25 | ザ、プロクター、エンド、ギャンブル、カンパニー | アルデヒドで官能化されたセルロース性繊維とポリマーから作られた湿潤強度を有する紙製品 |
US20090191243A9 (en) | 2000-01-03 | 2009-07-30 | Hill John C | High unsaponifiables and methods of using the same and its derivatives and uses thereof |
US8529970B2 (en) | 2000-01-03 | 2013-09-10 | International Flora Technologies, Ltd. | High unsaponifiables and methods of using the same |
FR2825628B1 (fr) | 2001-06-07 | 2004-03-19 | Oreal | Composition cosmetique comportant un polymere comprenant des groupes de jonction capables d'etablir chacun au moins trois liaisons h |
FR2894816B1 (fr) * | 2005-12-16 | 2008-02-01 | Oreal | Composition cosmetique ou pharmaceutique comprenant un copolymere comportant au moins un groupe ionisable, et procede de traitement cosmetique |
CN111939093B (zh) * | 2020-08-26 | 2023-04-07 | 广州市逸轩精细化工有限公司 | 一种具有发泡性和滋润性的沐浴油及其制备方法 |
-
1970
- 1970-01-19 CA CA072494A patent/CA921629A/en not_active Expired
- 1970-01-29 NL NL7001258A patent/NL7001258A/xx not_active Application Discontinuation
- 1970-02-04 DE DE2005084A patent/DE2005084C3/de not_active Expired
- 1970-02-11 CH CH197670A patent/CH537437A/de not_active IP Right Cessation
- 1970-02-13 FR FR7005150A patent/FR2034760B1/fr not_active Expired
- 1970-02-16 NO NO535/70A patent/NO132415C/no unknown
- 1970-02-16 BE BE746015D patent/BE746015A/fr not_active IP Right Cessation
- 1970-02-16 JP JP45013341A patent/JPS4924223B1/ja active Pending
- 1970-02-16 SE SE01931/70A patent/SE354783B/xx unknown
- 1970-02-16 DK DK74770*#A patent/DK125956C/da not_active IP Right Cessation
- 1970-02-17 GB GB1296241D patent/GB1296241A/en not_active Expired
- 1970-02-17 AT AT142270A patent/AT323328B/de not_active IP Right Cessation
-
1972
- 1972-02-14 US US00225994A patent/US3784488A/en not_active Expired - Lifetime
-
1973
- 1973-12-30 MY MY339/73A patent/MY7300339A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
NL7001258A (fr) | 1970-08-19 |
FR2034760B1 (fr) | 1975-05-30 |
NO132415C (fr) | 1975-11-12 |
SE354783B (fr) | 1973-03-26 |
DE2005084C3 (de) | 1979-06-13 |
US3784488A (en) | 1974-01-08 |
DE2005084A1 (de) | 1970-08-20 |
CH537437A (de) | 1973-05-31 |
GB1296241A (fr) | 1972-11-15 |
FR2034760A1 (fr) | 1970-12-18 |
CA921629A (en) | 1973-02-20 |
DK125956B (da) | 1973-05-28 |
MY7300339A (en) | 1973-12-31 |
DK125956C (da) | 1976-03-01 |
JPS4924223B1 (fr) | 1974-06-21 |
DE2005084B2 (de) | 1978-10-19 |
BE746015A (fr) | 1970-08-17 |
AT323328B (de) | 1975-07-10 |
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