JP2010504992A5 - - Google Patents

Info

Publication number

JP2010504992A5

JP2010504992A5 JP2009530543A JP2009530543A JP2010504992A5 JP 2010504992 A5 JP2010504992 A5 JP 2010504992A5 JP 2009530543 A JP2009530543 A JP 2009530543A JP 2009530543 A JP2009530543 A JP 2009530543A JP 2010504992 A5 JP2010504992 A5 JP 2010504992A5

Authority

JP

Japan

Prior art keywords

substitution

personal care

care composition

substituents

cellulose ether

Prior art date

2007-09-24

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.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• 239000000203 mixture Substances 0.000 claims 12
• 238000006467 substitution reaction Methods 0.000 claims 12
• 125000001424 substituent group Chemical group 0.000 claims 10
• 229920003086 cellulose ether Polymers 0.000 claims 7
• 230000002209 hydrophobic effect Effects 0.000 claims 7
• TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 claims 6
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
• 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims 3
• 239000004354 Hydroxyethyl cellulose Substances 0.000 claims 3
• 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims 3
• 229910052757 nitrogen Inorganic materials 0.000 claims 2
• 239000004094 surface-active agent Substances 0.000 claims 2
• 125000002877 alkyl aryl group Chemical group 0.000 claims 1
• 125000000217 alkyl group Chemical group 0.000 claims 1
• 150000001350 alkyl halides Chemical class 0.000 claims 1
• 150000001450 anions Chemical class 0.000 claims 1
• 125000003710 aryl alkyl group Chemical group 0.000 claims 1
• WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical group OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 1
• 125000004432 carbon atom Chemical group C* 0.000 claims 1
• 125000002091 cationic group Chemical group 0.000 claims 1
• MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 claims 1
• 229940073507 cocamidopropyl betaine Drugs 0.000 claims 1
• GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 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
• 150000002118 epoxides Chemical class 0.000 claims 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
• -1 hydroxyethyl groups Chemical group 0.000 claims 1
• 238000000034 method Methods 0.000 claims 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
• BOUCRWJEKAGKKG-UHFFFAOYSA-N n-[3-(diethylaminomethyl)-4-hydroxyphenyl]acetamide Chemical compound CCN(CC)CC1=CC(NC(C)=O)=CC=C1O BOUCRWJEKAGKKG-UHFFFAOYSA-N 0.000 claims 1
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
• 238000005956 quaternization reaction Methods 0.000 claims 1
• 229940057950 sodium laureth sulfate Drugs 0.000 claims 1
• SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 claims 1
• 239000004711 α-olefin Substances 0.000 claims 1