DE3133078A1 - "1,3-dialkyl-cyclohexan-verbindungen, verfahren zu deren herstellung und deren verwendung" - Google Patents
"1,3-dialkyl-cyclohexan-verbindungen, verfahren zu deren herstellung und deren verwendung"Info
- Publication number
- DE3133078A1 DE3133078A1 DE19813133078 DE3133078A DE3133078A1 DE 3133078 A1 DE3133078 A1 DE 3133078A1 DE 19813133078 DE19813133078 DE 19813133078 DE 3133078 A DE3133078 A DE 3133078A DE 3133078 A1 DE3133078 A1 DE 3133078A1
- Authority
- DE
- Germany
- Prior art keywords
- compounds
- alkyl radical
- compound
- cyclohexane
- dialkylcyclohexane
- 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- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 title abstract description 8
- 239000002537 cosmetic Substances 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000002360 preparation method Methods 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 16
- -1 alkyl radical Chemical class 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- 239000010941 cobalt Substances 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- 239000002671 adjuvant Substances 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 abstract 2
- 239000003921 oil Substances 0.000 description 10
- JHIVVAPYMSGYDF-PTQBSOBMSA-N cyclohexanone Chemical class O=[13C]1CCCCC1 JHIVVAPYMSGYDF-PTQBSOBMSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- 239000006071 cream Substances 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical class OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- DFIIJEHQGUKXKU-UHFFFAOYSA-N 1,3-bis(2-ethylhexyl)cyclohexane Chemical compound CCCCC(CC)CC1CCCC(CC(CC)CCCC)C1 DFIIJEHQGUKXKU-UHFFFAOYSA-N 0.000 description 2
- MEVPWSGMRKHLRE-UHFFFAOYSA-N 2,6-bis(2-ethylhexyl)cyclohexan-1-ol Chemical compound CCCCC(CC)CC1CCCC(CC(CC)CCCC)C1O MEVPWSGMRKHLRE-UHFFFAOYSA-N 0.000 description 2
- 241001440269 Cutina Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229940099259 vaseline Drugs 0.000 description 2
- MQYCFSAJJYAGBT-UHFFFAOYSA-N 1,3-bis(2-ethylbutyl)cyclohexane Chemical compound CCC(CC)CC1CCCC(CC(CC)CC)C1 MQYCFSAJJYAGBT-UHFFFAOYSA-N 0.000 description 1
- ZTLNZCYWGKJKGG-UHFFFAOYSA-N 1,3-bis(2-methylpentyl)cyclohexane Chemical compound CCCC(C)CC1CCCC(CC(C)CCC)C1 ZTLNZCYWGKJKGG-UHFFFAOYSA-N 0.000 description 1
- NTMWTTZDCVXCPC-UHFFFAOYSA-N 2,6-bis(2-ethylbutyl)cyclohexan-1-ol Chemical compound CCC(CC)CC1CCCC(CC(CC)CC)C1O NTMWTTZDCVXCPC-UHFFFAOYSA-N 0.000 description 1
- HSKXCNUDQDBQLC-UHFFFAOYSA-N 2,6-bis(2-methylpentyl)cyclohexan-1-ol Chemical compound CCCC(C)CC1CCCC(CC(C)CCC)C1O HSKXCNUDQDBQLC-UHFFFAOYSA-N 0.000 description 1
- KLDIFXMGDDZVFI-UHFFFAOYSA-N 2,6-bis(2-methylpropyl)cyclohexan-1-ol Chemical compound CC(C)CC1CCCC(CC(C)C)C1O KLDIFXMGDDZVFI-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 238000007869 Guerbet synthesis reaction Methods 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 244000078856 Prunus padus Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 238000005882 aldol condensation reaction Methods 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 238000009835 boiling Methods 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
- 239000004202 carbamide Substances 0.000 description 1
- 229940082500 cetostearyl alcohol Drugs 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 239000008278 cosmetic cream Substances 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- HPXRVTGHNJAIIH-PTQBSOBMSA-N cyclohexanol Chemical class O[13CH]1CCCCC1 HPXRVTGHNJAIIH-PTQBSOBMSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940116364 hard fat Drugs 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003883 ointment base Substances 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 230000010181 polygamy Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000002884 skin cream Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- 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
- A61K8/31—Hydrocarbons
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/22—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms by reduction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/02—Monocyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/16—Monocyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with a six-membered ring
- C07C13/18—Monocyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with a six-membered ring with a cyclohexane ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
- C07C2523/42—Platinum
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
- C07C2523/44—Palladium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/745—Iron
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/75—Cobalt
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/755—Nickel
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813133078 DE3133078A1 (de) | 1981-08-21 | 1981-08-21 | "1,3-dialkyl-cyclohexan-verbindungen, verfahren zu deren herstellung und deren verwendung" |
| US06/332,950 US4457944A (en) | 1981-08-21 | 1981-12-21 | 1,3-Dialkyl-cyclohexanes, method of production and method of use in cosmetics |
| EP82107362A EP0072988B1 (de) | 1981-08-21 | 1982-08-13 | Verwendung von 1,3-Dialkyl-cyclohexan-Verbindungen als kosmetische Ölkomponente |
| AT82107362T ATE15882T1 (de) | 1981-08-21 | 1982-08-13 | Verwendung von 1,3-dialkyl-cyclohexanverbindungen als kosmetische oelkomponente. |
| DE8282107362T DE3266700D1 (en) | 1981-08-21 | 1982-08-13 | Use of 1,3-dialkylcyclohexanes as cosmetical oil component |
| JP57143475A JPS5841826A (ja) | 1981-08-21 | 1982-08-20 | １．３―ジアルキルシクロヘキサン化合物を含有する化粧品 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813133078 DE3133078A1 (de) | 1981-08-21 | 1981-08-21 | "1,3-dialkyl-cyclohexan-verbindungen, verfahren zu deren herstellung und deren verwendung" |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3133078A1 true DE3133078A1 (de) | 1983-03-10 |
Family
ID=6139784
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19813133078 Withdrawn DE3133078A1 (de) | 1981-08-21 | 1981-08-21 | "1,3-dialkyl-cyclohexan-verbindungen, verfahren zu deren herstellung und deren verwendung" |
| DE8282107362T Expired DE3266700D1 (en) | 1981-08-21 | 1982-08-13 | Use of 1,3-dialkylcyclohexanes as cosmetical oil component |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE8282107362T Expired DE3266700D1 (en) | 1981-08-21 | 1982-08-13 | Use of 1,3-dialkylcyclohexanes as cosmetical oil component |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4457944A (enExample) |
| EP (1) | EP0072988B1 (enExample) |
| JP (1) | JPS5841826A (enExample) |
| AT (1) | ATE15882T1 (enExample) |
| DE (2) | DE3133078A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19623383A1 (de) * | 1996-06-12 | 1997-12-18 | Henkel Kgaa | Verwendung von Fettstoffen als Siliconersatz zur Herstellung von kosmetischen und/oder pharmazeutischen Zubereitungen |
| WO2002024621A1 (de) * | 2000-09-20 | 2002-03-28 | Cognis Deutschland Gmbh & Co. Kg | Verfahren zur herstellung von verzweigten alkoholen und/oder kohlenwasserstoffen |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3226753A1 (de) * | 1982-07-14 | 1984-01-19 | Schering AG, 1000 Berlin und 4709 Bergkamen | Wundverband zur aufnahme von wundsekret |
| DE3507175A1 (de) * | 1985-03-01 | 1986-09-04 | Basf Ag, 6700 Ludwigshafen | Dicyclohexylalkane, ihre herstellung, diese enthaltende kosmetische und pharmazeutische zubereitungen und ihre verwendung als oelkomponente |
| JPS62262974A (ja) * | 1986-05-10 | 1987-11-16 | Daiei Giken Kk | 包子の製造装置 |
| JPS62262975A (ja) * | 1986-05-10 | 1987-11-16 | Daiei Giken Kk | 包子の製造装置 |
| US4847073A (en) * | 1988-06-29 | 1989-07-11 | Ici Americas Inc. | Ultraviolet radiation absorbing cyclohexenylidene method |
| JP2006256980A (ja) * | 2005-03-15 | 2006-09-28 | Schwarzkopf & Henkel Kk | 染毛剤組成物 |
| US7998339B2 (en) * | 2005-12-12 | 2011-08-16 | Neste Oil Oyj | Process for producing a hydrocarbon component |
| US7850841B2 (en) * | 2005-12-12 | 2010-12-14 | Neste Oil Oyj | Process for producing a branched hydrocarbon base oil from a feedstock containing aldehyde and/or ketone |
| US7501546B2 (en) * | 2005-12-12 | 2009-03-10 | Neste Oil Oj | Process for producing a branched hydrocarbon component |
| US7888542B2 (en) * | 2005-12-12 | 2011-02-15 | Neste Oil Oyj | Process for producing a saturated hydrocarbon component |
| US8053614B2 (en) | 2005-12-12 | 2011-11-08 | Neste Oil Oyj | Base oil |
| KR101264148B1 (ko) * | 2011-01-18 | 2013-05-14 | 한화케미칼 주식회사 | 디에틸헥실사이클로헥산을 포함하는 벽지용 염화비닐계 수지 조성물 |
| EP3322488B1 (en) * | 2015-07-15 | 2022-11-30 | Bakel S.R.L. | Cosmetic composition |
| US9857006B2 (en) | 2016-03-31 | 2018-01-02 | Quick Fitting, Inc. | Retaining ring for pipe joint devices |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3748231A (en) * | 1972-01-27 | 1973-07-24 | Sun Research Development | Microbiological oxidation of alkyl-substituted cyclic compounds |
| CH616645A5 (enExample) * | 1975-11-17 | 1980-04-15 | Roure Bertrand Dupont Sa | |
| US4206090A (en) * | 1978-10-06 | 1980-06-03 | International Flavors & Fragrances Inc. | 3-Methyl-1-phenyl-pentanol-5 or its isomer and butanoyl cyclohexane derivatives |
-
1981
- 1981-08-21 DE DE19813133078 patent/DE3133078A1/de not_active Withdrawn
- 1981-12-21 US US06/332,950 patent/US4457944A/en not_active Expired - Lifetime
-
1982
- 1982-08-13 EP EP82107362A patent/EP0072988B1/de not_active Expired
- 1982-08-13 AT AT82107362T patent/ATE15882T1/de not_active IP Right Cessation
- 1982-08-13 DE DE8282107362T patent/DE3266700D1/de not_active Expired
- 1982-08-20 JP JP57143475A patent/JPS5841826A/ja active Granted
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19623383A1 (de) * | 1996-06-12 | 1997-12-18 | Henkel Kgaa | Verwendung von Fettstoffen als Siliconersatz zur Herstellung von kosmetischen und/oder pharmazeutischen Zubereitungen |
| DE19623383C2 (de) * | 1996-06-12 | 1999-07-01 | Henkel Kgaa | Verwendung von Fettstoffen als Siliconersatz zur Herstellung von kosmetischen und/oder pharmazeutischen Zubereitungen |
| US6432419B2 (en) | 1996-06-12 | 2002-08-13 | Cognis Deutschland Gmbh | Use of fats to replace silicone in cosmetic and/or pharmaceutical preparations |
| WO2002024621A1 (de) * | 2000-09-20 | 2002-03-28 | Cognis Deutschland Gmbh & Co. Kg | Verfahren zur herstellung von verzweigten alkoholen und/oder kohlenwasserstoffen |
| US7365235B2 (en) | 2000-09-20 | 2008-04-29 | Cognis Deutschland Gmbh & Co. Kg | Processes for producing branched compounds via condensation and hydrogenation |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0354082B2 (enExample) | 1991-08-19 |
| JPS5841826A (ja) | 1983-03-11 |
| EP0072988B1 (de) | 1985-10-02 |
| DE3266700D1 (en) | 1985-11-07 |
| ATE15882T1 (de) | 1985-10-15 |
| US4457944A (en) | 1984-07-03 |
| EP0072988A1 (de) | 1983-03-02 |
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