JP2008512362A5 - - Google Patents

Info

Publication number

JP2008512362A5

JP2008512362A5 JP2007529310A JP2007529310A JP2008512362A5 JP 2008512362 A5 JP2008512362 A5 JP 2008512362A5 JP 2007529310 A JP2007529310 A JP 2007529310A JP 2007529310 A JP2007529310 A JP 2007529310A JP 2008512362 A5 JP2008512362 A5 JP 2008512362A5

Authority

JP

Japan

Prior art keywords

products

compound

antifungal

antibacterial

malodor neutralizing

Prior art date

2005-08-31

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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• 150000001875 compounds Chemical class 0.000 claims 18
• -1 ester compound Chemical class 0.000 claims 9
• 230000000844 anti-bacterial effect Effects 0.000 claims 8
• 230000000843 anti-fungal effect Effects 0.000 claims 8
• 229940121375 antifungal agent Drugs 0.000 claims 8
• 230000003472 neutralizing effect Effects 0.000 claims 8
• 239000000203 mixture Substances 0.000 claims 5
• 239000002537 cosmetic Substances 0.000 claims 4
• 239000003205 fragrance Substances 0.000 claims 4
• 239000000463 material Substances 0.000 claims 4
• 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 3
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
• 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 claims 3
• 238000004519 manufacturing process Methods 0.000 claims 3
• 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 3
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
• 229920006395 saturated elastomer Polymers 0.000 claims 3
• 150000001449 anionic compounds Chemical group 0.000 claims 2
• 125000004432 carbon atom Chemical group C* 0.000 claims 2
• 239000003795 chemical substances by application Substances 0.000 claims 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
• 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
• 229910001412 inorganic anion Inorganic materials 0.000 claims 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
• 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 claims 2
• SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 1
• 125000002704 decyl 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])* 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
• 238000000034 method Methods 0.000 claims 1
• 125000001400 nonyl 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])[H] 0.000 claims 1
• BEUQATKTSHPNNY-UHFFFAOYSA-N octan-3-yl 2-hydroxyacetate Chemical compound CCCCCC(CC)OC(=O)CO BEUQATKTSHPNNY-UHFFFAOYSA-N 0.000 claims 1
• 229930195734 saturated hydrocarbon Natural products 0.000 claims 1
• 125000002948 undecyl 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])[H] 0.000 claims 1