DD141454A1 - Lichtschutzmittel - Google Patents
Lichtschutzmittel Download PDFInfo
- Publication number
- DD141454A1 DD141454A1 DD21071377A DD21071377A DD141454A1 DD 141454 A1 DD141454 A1 DD 141454A1 DD 21071377 A DD21071377 A DD 21071377A DD 21071377 A DD21071377 A DD 21071377A DD 141454 A1 DD141454 A1 DD 141454A1
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- cation
- compounds
- protection means
- sun protection
- radical
- Prior art date
Links
- 230000037072 sun protection Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000000516 sunscreening agent Substances 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CIIDQQXQGARXMA-UHFFFAOYSA-N 2-(2-phenylfuran-3-yl)prop-2-enoic acid Chemical compound C1=COC(C=2C=CC=CC=2)=C1C(=C)C(=O)O CIIDQQXQGARXMA-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 235000013985 cinnamic acid Nutrition 0.000 description 2
- 239000002285 corn oil Substances 0.000 description 2
- 235000005687 corn oil Nutrition 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 2
- 239000001814 pectin Substances 0.000 description 2
- 235000010987 pectin Nutrition 0.000 description 2
- 229920001277 pectin Polymers 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 230000000622 irritating effect Effects 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Furan Compounds (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BG7633962A BG23482A1 (en) | 1976-08-09 | 1976-08-09 | Salts of 2- phenyl- 3- furil- 2- propene acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD141454A1 true DD141454A1 (de) | 1980-05-07 |
Family
ID=3902505
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD21071377A DD141454A1 (de) | 1976-08-09 | 1977-08-08 | Lichtschutzmittel |
| DD20049077A DD133236A1 (de) | 1976-08-09 | 1977-08-08 | Verfahren zur herstellung von 2-phenyl-3-furyl-2-propensaeure und deren derivaten |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD20049077A DD133236A1 (de) | 1976-08-09 | 1977-08-08 | Verfahren zur herstellung von 2-phenyl-3-furyl-2-propensaeure und deren derivaten |
Country Status (8)
| Country | Link |
|---|---|
| BG (1) | BG23482A1 (cs) |
| CS (1) | CS202170B1 (cs) |
| DD (2) | DD141454A1 (cs) |
| DE (1) | DE2735871A1 (cs) |
| ES (1) | ES461922A1 (cs) |
| FR (1) | FR2361379A1 (cs) |
| GR (1) | GR63993B (cs) |
| IT (1) | IT1115891B (cs) |
-
1976
- 1976-08-09 BG BG7633962A patent/BG23482A1/xx unknown
-
1977
- 1977-08-08 FR FR7724393A patent/FR2361379A1/fr active Granted
- 1977-08-08 DD DD21071377A patent/DD141454A1/de unknown
- 1977-08-08 DD DD20049077A patent/DD133236A1/xx unknown
- 1977-08-09 GR GR54121A patent/GR63993B/el unknown
- 1977-08-09 IT IT5060877A patent/IT1115891B/it active
- 1977-08-09 CS CS526577A patent/CS202170B1/cs unknown
- 1977-08-09 DE DE19772735871 patent/DE2735871A1/de not_active Withdrawn
- 1977-08-27 ES ES461922A patent/ES461922A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2361379A1 (fr) | 1978-03-10 |
| FR2361379B3 (cs) | 1980-08-22 |
| CS202170B1 (en) | 1980-12-31 |
| IT1115891B (it) | 1986-02-10 |
| BG23482A1 (en) | 1979-12-12 |
| ES461922A1 (es) | 1979-01-16 |
| DE2735871A1 (de) | 1978-02-23 |
| GR63993B (en) | 1980-01-18 |
| DD133236A1 (de) | 1978-12-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69918775T2 (de) | Ein Bärentraübenextrakt und ein Reduktionsmittel enthaltende Hautdepigmentierungszusammensetzung | |
| DE3441636C2 (de) | Ultraviolett-Absorber, enthaltend neue Chalkon-Derivate | |
| DE69202831T2 (de) | Depigmentiermittel Arbutosid enthaltend. | |
| DE3415413C2 (cs) | ||
| DE69010047T2 (de) | Hydrophile Derivate von Benzylidenkampfer enthaltende kosmetische und pharmazeutische Zusammensetzungen und sulfonierte hydrophile Derivate von Benzylidenkampfer. | |
| US4518614A (en) | Cosmetic preparation | |
| DE3010572A1 (de) | Hautpflege- und hautschutzpraeparate | |
| DE3403846A1 (de) | Kosmetisches mittel zum schutz vor uv-strahlung sowie anwendungsverfahren desselben | |
| DE3113177C2 (cs) | ||
| DE3427240A1 (de) | Antiinflammatorische und antipyretische creme | |
| DE69700147T2 (de) | Verwendung von mindestens einem Glykol zur Solubilisierung von Melatonin in Wasser und sie enthaltende Zusammensetzungen | |
| DE1617704B2 (de) | Haarbehandlungsmittel | |
| DE69700042T2 (de) | Stabile gelierte Zusammensetzung, die gegenüber Sauerstoff und/oder Wasser empfindliche lipophile Wirkstoffe enthält | |
| DE2728922C3 (de) | Glycerintri-3,5,5-trimethylhexanoat | |
| EP0044975A1 (de) | Polyalkoxycarbinolzimtsäureester, Verfahren zu ihrer Herstellung und diese enthaltende Lichtschutzmittel | |
| DE69120992T2 (de) | Alkyldiamide und kosmetische Behandlungszusammensetzungen | |
| DD141454A1 (de) | Lichtschutzmittel | |
| EP0119516B1 (de) | 3-Amino-tetrahydro-1,3-thiazin-2,4-dione, ihre Verwendung sowie diese Verbindungen enthaltende Hautbehandlungsmittel | |
| DE3028417A1 (de) | Neue veraetherte p-hydroxyzimtsaeureester, ihre herstellung und diese enthaltende zubereitungen als lichtschutzmittel | |
| EP0044970B1 (de) | Verwendung von verätherten 2-(4-Hydroxybenzyliden)-gamma-butyrolactonen als Lichtschutzmittel | |
| EP0095097B1 (de) | Gegebenenfalls in Form eines Salzes vorliegendes Zimtsäure-(p-sulfo-phenylamid), ein Verfahren zu seiner Herstellung und seine Verwendung in Lichtschutzmitteln | |
| DE2514878A1 (de) | Allantoin-ascorbinsaeure-komplex | |
| DE2509646A1 (de) | Neue derivate der dialkylaminoalkyl-p-dialkyl-aminobenzoesaeureester | |
| DE3133425A1 (de) | "percarbonsaeuren als antiseborrohische zusaetze fuer kosmetische mittel" | |
| DE3049123A1 (de) | Fettsaeureester von 4-isopropyltropolon und hautverschoenerndes, kosmetisches mittel |