CA1050382A - Surfactant iodine composition and method for preparing same - Google Patents
Surfactant iodine composition and method for preparing sameInfo
- Publication number
- CA1050382A CA1050382A CA226,350A CA226350A CA1050382A CA 1050382 A CA1050382 A CA 1050382A CA 226350 A CA226350 A CA 226350A CA 1050382 A CA1050382 A CA 1050382A
- Authority
- CA
- Canada
- Prior art keywords
- iodine
- surfactant
- iodide
- composition
- nonionic
- 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.)
- Expired
Links
- 229910052740 iodine Inorganic materials 0.000 title claims abstract description 133
- 239000011630 iodine Substances 0.000 title claims abstract description 126
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 title claims abstract description 100
- 239000000203 mixture Substances 0.000 title claims abstract description 78
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 54
- 238000000034 method Methods 0.000 title claims abstract description 33
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 19
- 229910001505 inorganic iodide Inorganic materials 0.000 claims abstract description 12
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 11
- 230000008569 process Effects 0.000 claims description 27
- 239000000463 material Substances 0.000 claims description 17
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 7
- 229940107816 ammonium iodide Drugs 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 125000002091 cationic group Chemical group 0.000 claims description 7
- 229910000043 hydrogen iodide Inorganic materials 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 229910001619 alkaline earth metal iodide Inorganic materials 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910001516 alkali metal iodide Inorganic materials 0.000 claims description 4
- 150000002894 organic compounds Chemical class 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000004694 iodide salts Chemical class 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 230000006872 improvement Effects 0.000 claims description 2
- 230000002070 germicidal effect Effects 0.000 abstract description 5
- 238000004140 cleaning Methods 0.000 abstract description 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract description 2
- 150000002496 iodine Chemical class 0.000 abstract 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Inorganic materials [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 17
- 238000004090 dissolution Methods 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000012467 final product Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000008859 change Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910001511 metal iodide Inorganic materials 0.000 description 3
- 238000011012 sanitization Methods 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- PWIDFFRKCKLPNI-UHFFFAOYSA-M [I+].[I-] Chemical compound [I+].[I-] PWIDFFRKCKLPNI-UHFFFAOYSA-M 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 229940087291 tridecyl alcohol Drugs 0.000 description 2
- STMRWVUTGPZZER-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=CC(O)=C1CC(C)C STMRWVUTGPZZER-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Polymers 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- -1 and alkaline earth Inorganic materials 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- SGUXGJPBTNFBAD-UHFFFAOYSA-L barium iodide Chemical class [I-].[I-].[Ba+2] SGUXGJPBTNFBAD-UHFFFAOYSA-L 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229910052729 chemical element Inorganic materials 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 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 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
- C11D3/485—Halophors, e.g. iodophors
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47942274A | 1974-06-14 | 1974-06-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1050382A true CA1050382A (en) | 1979-03-13 |
Family
ID=23903941
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA226,350A Expired CA1050382A (en) | 1974-06-14 | 1975-05-06 | Surfactant iodine composition and method for preparing same |
Country Status (10)
Country | Link |
---|---|
JP (1) | JPS5118284A (cs) |
BR (1) | BR7503220A (cs) |
CA (1) | CA1050382A (cs) |
CH (1) | CH595436A5 (cs) |
DE (1) | DE2524388A1 (cs) |
FR (1) | FR2274681A1 (cs) |
GB (1) | GB1467614A (cs) |
MX (1) | MX3302E (cs) |
NL (1) | NL7507060A (cs) |
ZA (1) | ZA752961B (cs) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989000006A1 (en) * | 1987-07-01 | 1989-01-12 | Novapharm Research Pty. Ltd. | Biocidal composition |
AU622413B2 (en) * | 1987-07-01 | 1992-04-09 | Novapharm Research Pty. Ltd. | Biocidal composition |
US5409697A (en) * | 1987-07-01 | 1995-04-25 | Novapharm Research Pty. Ltd. | Biocidal composition |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4355021A (en) * | 1980-10-29 | 1982-10-19 | S. C. Johnson & Son, Inc. | Virucidal wipe and method |
NO168565C (no) * | 1983-03-02 | 1992-03-11 | Euro Celtique Sa | Fremgangsmaate for fremstilling av standardiserte jodoforpreparater |
EP0145223B1 (en) * | 1983-11-04 | 1990-02-28 | Mario Flores Rivera | Highly stable free iodine iodophor compositions, process for preparing same and process for using same |
US4818532A (en) * | 1986-10-23 | 1989-04-04 | Ppg Industries, Inc. | Bromophor composition |
US4804492A (en) * | 1986-11-07 | 1989-02-14 | Sterling Drug Inc. | Liquid sanitizing and cleaning compositions with diminished skin irritancy |
US5049299A (en) * | 1989-10-26 | 1991-09-17 | Kiwi Brands Incorporated | Liquid lavatory cleansing and sanitizing composition |
JP2002525418A (ja) * | 1998-09-25 | 2002-08-13 | ザ、プロクター、エンド、ギャンブル、カンパニー | 抗菌洗剤組成物 |
-
1975
- 1975-05-06 CA CA226,350A patent/CA1050382A/en not_active Expired
- 1975-05-07 ZA ZA00752961A patent/ZA752961B/xx unknown
- 1975-05-14 GB GB2044475A patent/GB1467614A/en not_active Expired
- 1975-05-22 BR BR4122/75A patent/BR7503220A/pt unknown
- 1975-05-29 JP JP50065189A patent/JPS5118284A/ja active Pending
- 1975-05-30 CH CH697275A patent/CH595436A5/xx not_active IP Right Cessation
- 1975-06-02 DE DE19752524388 patent/DE2524388A1/de not_active Withdrawn
- 1975-06-05 MX MX001269U patent/MX3302E/es unknown
- 1975-06-12 FR FR7518416A patent/FR2274681A1/fr active Granted
- 1975-06-13 NL NL7507060A patent/NL7507060A/xx not_active Application Discontinuation
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989000006A1 (en) * | 1987-07-01 | 1989-01-12 | Novapharm Research Pty. Ltd. | Biocidal composition |
AU622413B2 (en) * | 1987-07-01 | 1992-04-09 | Novapharm Research Pty. Ltd. | Biocidal composition |
US5409697A (en) * | 1987-07-01 | 1995-04-25 | Novapharm Research Pty. Ltd. | Biocidal composition |
Also Published As
Publication number | Publication date |
---|---|
MX3302E (es) | 1980-09-03 |
ZA752961B (en) | 1976-03-31 |
FR2274681A1 (fr) | 1976-01-09 |
NL7507060A (nl) | 1975-12-16 |
BR7503220A (pt) | 1976-06-29 |
JPS5118284A (cs) | 1976-02-13 |
AU8094975A (en) | 1976-11-11 |
GB1467614A (en) | 1977-03-16 |
CH595436A5 (cs) | 1978-02-15 |
FR2274681B1 (cs) | 1979-06-08 |
DE2524388A1 (de) | 1976-01-02 |
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