JP2002080681A

JP2002080681A - 芳香および／または消臭用ゲル状組成物

芳香および／または消臭用ゲル状組成物

Info

Publication number: JP2002080681A
Authority: JP; Japan
Prior art keywords: component; gel composition; mass; deodorant; aroma
Prior art date: 2000-09-11
Legal status : Pending

Application number

JP2000274553A

Other languages

English (en)

Japanese (ja)

Other versions

JP2002080681A5 (enExample

Inventor

Tetsuya Ishii

徹弥石井

Tetsuo Wada

哲夫和田

Current Assignee

Resonac Holdings Corp

Original Assignee

Showa Denko KK

Priority date

2000-09-11

Filing date

2000-09-11

Publication date

2002-03-19

2000-09-11 Application filed by Showa Denko KK filed Critical Showa Denko KK

2000-09-11 Priority to JP2000274553A priority Critical patent/JP2002080681A/ja

2002-03-19 Publication of JP2002080681A publication Critical patent/JP2002080681A/ja

2007-08-30 Publication of JP2002080681A5 publication Critical patent/JP2002080681A5/ja

Status Pending legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 65
239000002781 deodorant agent Substances 0.000 title claims abstract description 54
229920001577 copolymer Polymers 0.000 claims abstract description 33
150000001875 compounds Chemical class 0.000 claims abstract description 29
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 claims abstract description 26
239000000178 monomer Substances 0.000 claims abstract description 25
229910052783 alkali metal Inorganic materials 0.000 claims abstract description 17
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
239000000499 gel Substances 0.000 claims description 97
-1 alkali metal salt Chemical class 0.000 claims description 73
239000003205 fragrance Substances 0.000 claims description 26
239000003431 cross linking reagent Substances 0.000 claims description 16
150000003863 ammonium salts Chemical class 0.000 claims description 13
229910052782 aluminium Inorganic materials 0.000 claims description 12
125000003118 aryl group Chemical group 0.000 claims description 12
238000004332 deodorization Methods 0.000 claims description 12
150000003839 salts Chemical class 0.000 claims description 7
238000004898 kneading Methods 0.000 claims description 6
239000004593 Epoxy Substances 0.000 claims description 5
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
229910052751 metal Inorganic materials 0.000 claims description 4
239000002184 metal Substances 0.000 claims description 4
239000003513 alkali Substances 0.000 claims 1
238000004132 cross linking Methods 0.000 abstract description 7
150000001340 alkali metals Chemical class 0.000 abstract description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 2
239000002361 compost Substances 0.000 abstract description 2
239000004971 Cross linker Substances 0.000 abstract 1
229920006037 cross link polymer Polymers 0.000 abstract 1
239000000126 substance Substances 0.000 description 32
239000000796 flavoring agent Substances 0.000 description 29
235000019634 flavors Nutrition 0.000 description 29
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PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 14
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235000014113 dietary fatty acids Nutrition 0.000 description 12
239000000194 fatty acid Substances 0.000 description 12
229930195729 fatty acid Natural products 0.000 description 12
239000007864 aqueous solution Substances 0.000 description 11
238000000034 method Methods 0.000 description 11
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HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 5
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239000000853 adhesive Substances 0.000 description 4
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VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
229940024545 aluminum hydroxide Drugs 0.000 description 4
230000007423 decrease Effects 0.000 description 4
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 4
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
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ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 4
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
238000000926 separation method Methods 0.000 description 4
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235000019698 starch Nutrition 0.000 description 4
238000013268 sustained release Methods 0.000 description 4
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MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
239000008371 vanilla flavor Substances 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
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GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 3
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