JP2005118776A5 - - Google Patents

Info

Publication number

JP2005118776A5

JP2005118776A5 JP2004299721A JP2004299721A JP2005118776A5 JP 2005118776 A5 JP2005118776 A5 JP 2005118776A5 JP 2004299721 A JP2004299721 A JP 2004299721A JP 2004299721 A JP2004299721 A JP 2004299721A JP 2005118776 A5 JP2005118776 A5 JP 2005118776A5

Authority

JP

Japan

Prior art keywords

weight

mass

oligoglycoside

carbon atoms

self

Prior art date

2004-10-14

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.)

Pending

Links

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• 239000000203 mixture Substances 0.000 claims description 14
• 125000005456 glyceride group Chemical group 0.000 claims description 9
• 239000002537 cosmetic Substances 0.000 claims description 7
• 239000008194 pharmaceutical composition Substances 0.000 claims description 6
• 125000004432 carbon atom Chemical group C* 0.000 claims description 5
• LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims description 4
• 125000000217 alkyl group Chemical group 0.000 claims description 4
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
• 239000004615 ingredient Substances 0.000 claims description 4
• 125000002252 acyl group Chemical group 0.000 claims description 2
• 238000004519 manufacturing process Methods 0.000 claims description 2
• 125000001424 substituent group Chemical group 0.000 claims description 2
• BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims 2
• GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims 2
• 125000003342 alkenyl group Chemical group 0.000 claims 1
• 229960000541 cetyl alcohol Drugs 0.000 claims 1
• 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
• 150000002191 fatty alcohols Chemical class 0.000 claims 1
• 125000001421 myristyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
• GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims 1
• 125000000913 palmityl 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])C([H])([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 claims 1
• 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([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 claims 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
• 239000003995 emulsifying agent Substances 0.000 description 5
• 230000001804 emulsifying effect Effects 0.000 description 5
• 239000000839 emulsion Substances 0.000 description 4
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
• DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
• 230000001166 anti-perspirative effect Effects 0.000 description 3
• 239000003213 antiperspirant Substances 0.000 description 3
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
• 238000009472 formulation Methods 0.000 description 2
• IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
• 230000007774 longterm Effects 0.000 description 2
• 239000007764 o/w emulsion Substances 0.000 description 2
• 208000035985 Body Odor Diseases 0.000 description 1
• 241001440269 Cutina Species 0.000 description 1
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
• 235000021314 Palmitic acid Nutrition 0.000 description 1
• 206010040904 Skin odour abnormal Diseases 0.000 description 1
• 235000021355 Stearic acid Nutrition 0.000 description 1
• 239000003125 aqueous solvent Substances 0.000 description 1
• 239000012752 auxiliary agent Substances 0.000 description 1
• OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
• 239000007957 coemulsifier Substances 0.000 description 1
• 239000008139 complexing agent Substances 0.000 description 1
• 230000007423 decrease Effects 0.000 description 1
• 230000000694 effects Effects 0.000 description 1
• WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
• QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
• OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
• 238000005191 phase separation Methods 0.000 description 1
• 239000008117 stearic acid Substances 0.000 description 1
• 210000000106 sweat gland Anatomy 0.000 description 1
• 239000002562 thickening agent Substances 0.000 description 1
• 150000003626 triacylglycerols Chemical class 0.000 description 1