AU604275B2 - Isotropic laundry detergents containing polymeric quaternary ammonium salts - Google Patents
Isotropic laundry detergents containing polymeric quaternary ammonium salts Download PDFInfo
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- AU604275B2 AU604275B2 AU81396/87A AU8139687A AU604275B2 AU 604275 B2 AU604275 B2 AU 604275B2 AU 81396/87 A AU81396/87 A AU 81396/87A AU 8139687 A AU8139687 A AU 8139687A AU 604275 B2 AU604275 B2 AU 604275B2
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- 239000003599 detergent Substances 0.000 title claims description 18
- 150000003242 quaternary ammonium salts Chemical class 0.000 title claims description 17
- 239000000203 mixture Substances 0.000 claims description 47
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 239000002736 nonionic surfactant Substances 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 16
- -1 dimethyliminio Chemical class 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
- 239000005977 Ethylene Substances 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000011012 sanitization Methods 0.000 claims description 6
- 125000006353 oxyethylene group Chemical group 0.000 claims description 5
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 4
- 101150065749 Churc1 gene Proteins 0.000 claims description 4
- 102100038239 Protein Churchill Human genes 0.000 claims description 4
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 3
- 239000003814 drug Substances 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 1
- 229960001040 ammonium chloride Drugs 0.000 claims 1
- 235000019270 ammonium chloride Nutrition 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000009472 formulation Methods 0.000 description 19
- 238000012360 testing method Methods 0.000 description 12
- 239000004094 surface-active agent Substances 0.000 description 9
- 238000004453 electron probe microanalysis Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- KJPHTXTWFHVJIG-UHFFFAOYSA-N n-ethyl-2-[(6-methoxypyridin-3-yl)-(2-methylphenyl)sulfonylamino]-n-(pyridin-3-ylmethyl)acetamide Chemical compound C=1C=C(OC)N=CC=1N(S(=O)(=O)C=1C(=CC=CC=1)C)CC(=O)N(CC)CC1=CC=CN=C1 KJPHTXTWFHVJIG-UHFFFAOYSA-N 0.000 description 7
- 239000002689 soil Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 6
- 230000000845 anti-microbial effect Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 description 4
- 230000036556 skin irritation Effects 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 206010015946 Eye irritation Diseases 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 206010040880 Skin irritation Diseases 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 231100000013 eye irritation Toxicity 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 231100000344 non-irritating Toxicity 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 231100000475 skin irritation Toxicity 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 230000002070 germicidal effect Effects 0.000 description 2
- 229920004918 nonoxynol-9 Polymers 0.000 description 2
- 229940087419 nonoxynol-9 Drugs 0.000 description 2
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 2
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- KUXGUCNZFCVULO-UHFFFAOYSA-N 2-(4-nonylphenoxy)ethanol Chemical class CCCCCCCCCC1=CC=C(OCCO)C=C1 KUXGUCNZFCVULO-UHFFFAOYSA-N 0.000 description 1
- ATBQNLZREVOGBO-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCO)C=C1 ATBQNLZREVOGBO-UHFFFAOYSA-N 0.000 description 1
- XXPRRHYTDCWGRP-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 XXPRRHYTDCWGRP-UHFFFAOYSA-N 0.000 description 1
- BPZYKPINOMFZGY-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO)cc1 BPZYKPINOMFZGY-UHFFFAOYSA-N 0.000 description 1
- HNLXNOZHXNSSPN-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCOCCOCCOCCO)C=C1 HNLXNOZHXNSSPN-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
- 241000894006 Bacteria Species 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- RODZIAKMFCIGPL-UHFFFAOYSA-N P.I.I Chemical compound P.I.I RODZIAKMFCIGPL-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 229940048866 lauramine oxide Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- KUEDAAUECWBMLW-UHFFFAOYSA-N n,n,n',n'-tetramethylbut-2-ene-1,4-diamine Chemical compound CN(C)CC=CCN(C)C KUEDAAUECWBMLW-UHFFFAOYSA-N 0.000 description 1
- IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 1
- UTTVXKGNTWZECK-UHFFFAOYSA-N n,n-dimethyloctadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)[O-] UTTVXKGNTWZECK-UHFFFAOYSA-N 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 229940078482 nonoxynol-8 Drugs 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 229920004908 octoxynol-13 Polymers 0.000 description 1
- 229920004903 octoxynol-7 Polymers 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940057981 stearalkonium chloride Drugs 0.000 description 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 description 1
- FQDIANVAWVHZIR-OWOJBTEDSA-N trans-1,4-Dichlorobutene Chemical compound ClC\C=C\CCl FQDIANVAWVHZIR-OWOJBTEDSA-N 0.000 description 1
- HHLJUSLZGFYWKW-UHFFFAOYSA-N triethanolamine hydrochloride Chemical compound Cl.OCCN(CCO)CCO HHLJUSLZGFYWKW-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Description
6o4 FORM COMMONWEALTH OF AUSTRALI; PATENTS ACT 1952 COMPLETE SPECIFICATION S275 S F Ref: 41826
A
(ORIGINAL)
FOR OFFICE USE: Class Int Class Complete Specification Lodged: Accepted: Published: 1 5 S. Priority: e r s Related Art: Name and Address of Applicant: Address for Service: Sterling Drug Inc.
Park Avenue New York New York 10016 UNITED STATES OF AMERICA Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Complete Specification for the invention entitled: Isotropic Laundry Detergents Containing Polymeric Quaternary Ammonium Salts The following statement is a full description of this invention, including the best method of performing it known to me/us 5845/4 A B ST RAC T Stable, isotropic liquid laundry detergent and sanitizer compositions comprising a polymeric linear quaternary ammonium salt, one or more nonionic surfactants and water.
00.
00 as c r C This invention relates to isotropic liquid laundry detergents containing polymeric quaternary ammonium salts in combination with one or more ronionic surfactants.
INFORMATION DISCLOSURE STATEMENT U.S. Patent 3,771,989 discloses polymeric polyelectrolytes, useful as algicides, having the o°o formula: 0000 o o SCH 2 CH CH -CHCH S
CH
3
CH
I 3 3 n where n is an integer from 4 to 40, with molecular weights ranging from 1,000 to 10,000, which are chemically designated poly[oxyethylene(dimethyliminio)ethylene(dimethyliminio)ethylene dichloride]. As far as is presently known, compounds of this class are not known to have useful bactericidal properties nor are they known to be useful for incorporation in laundry detergents.
U.S. Patents 3,931,319; 4,001,432 and 4,012,446 disclose so-called "capped" polymers useful as "microbiocidal" agents, which have linear polymeric quaternary chains terminated by quaternary ammonium moieties, having the formula: +R RIV+cH2 C 2R'R"-CH2CR+ NR RIVRVCH CH=HCH R'R R-CHCH=CHCH NR RVRV 2nX 2 2 2n 1 2where X- is halide and "n is an integer from about 2 to about 30; where R' and R" may be either a primary or secondary alkyl radical having from 1 to 20 carbon atoms, hydroxy or dihydroxy derivatives of R' and benzyl, or benzyl containing at least one alkyl group where Z consists of from one to three aliphatic divalent radicals, each of which has 2 to carbon atoms, each aliphatic radical containing 0 to o 2 double bonds and 0 to 2 hydroxy substituents" and where *Geo o II
I
oOO 10 "R RI and RV may be either primary or secondary 00 0 I a 0 o alkyl containing from 1 to 20 carbon atoms, or hydroxy- 0 0 f 0 ethyl0 ethl U.S. Patent 4,027,020 discloses so-
U.S
called "randomly terminated" capped linear quaternary ammonium polymers generally similar to those described in U.S. Patents 3,931,319; 4,001,432 and 4,012,446 above prepared by reaction of a l,4-dihalo-2-butene, XCH 2
CH=
Ii CHCH 2 X, where X is halogen, with a mixture of a difunc- I tional tertiary amine: I R I R 1 1 .7 N Z A
R
and a monofunctional tertiary amine: I III
IV
R N-RIV
IV
R
The compounds are said to be effective against bacteria and algae and to a lesser extent against fungi. They -3are also stated to be non-foaming, a property which is said to be important in anti-microbial agents used in products and processes where the generation of foam is undesirable.
U.S. Patent 4,091,113 discloses "randomly terminated" capped linear quaternary ammonium polymers prepared in the same manner as described in U.S.
Patent 4,027,020 supra. The quaternaries are said to be "uniquely excellent hair conditioning agents" which 0 00 0001 i0 are "compatible in binary or tertiary systems with most oooo 0 o0 0o O of the lathering and cleansing surfactants used in hair 0o Q- 0 0 S conditioning consumer products". The patentee states 000000 I 0 oo that 40% aqueous solutions are non-irritating to the skin and that 4% aqueous solutions are non-irritating S 15 to the eyes. More specifically, the quaternaries are described as being compatible with surfactants and emulsifiers of the cationic, nonionic, amine oxide, alkylolamide, amphoteric, aminoacetic or 8-aminopropionic acid and betaine or betaine salt classes. The compositions I 20 are exemplified in Examples 28, 29 and 30 by formulations Scontaining the polymeric quaternary which is produced by reaction of 1,4-bis-dimethylamino-2-butene, triethanolamine and 1,4-dichloro-2-butene in water in combination with surfactants of the cationic (AMMONYX 4, i.e. stearalkonium chloride -Example 30), nonionic (TERGITOL 15-S-12, i.e. pareth-15-12 Example 29), alkylolamide (ONYXOL* 42, i.e. stearyl diethanolamide Example 30 and SUPER AMIDE* GR, i.e. cocoyldiethanolamide Example 28), amphoteric (MIRANOL* C-2M-SF, i.e. cocoamphocarboxypropionate and SANDOPAN* TFL, i.e. oleoamphopropylsulfonate -4both Example 28) and anionic (MAPROFIX* 60S, i.e. sodium laureth sulfate Example 28) classes. As far as is presently known the compounds of the structural type disclosed in U.S. Patents 3,931,319; 4,001,432; 4,012,446; 4,027,020 and 4,091,113 above are not known to have been previously incorporated in laundry detergents.
U.S. Patent 4,333,862 discloses, as one possible cationic surfactant in liquid detergent compositions containing an anionic, a cationic and a 10 nonionic surfactant, polyammonium salts of the formula: R r R 4 1 I. F- C
I!
0 Q0o 0 0 0 0 00 o ao o O00 Oo 0 0 o o o0 00oooo o o o t Sc R -N 3
I
R
R
4
.Z
where R 3 is C 8
-C
20 alkyl, alkenyl or aralkyl; each
R
4 is C1-C 4 alkyl or hydroxyalkyl; n is from 1 to 6; and n is from 1 to 3.
As noted above, polymeric linear quaternary ammonium salts of the structural types represented by those disclosed in U.S. Patents 3,771,989; 3,931319; 4,001,432; 4,012,446; 4,027,020 and 4,091,113 are not known to have been incorporated in laundry detergents. We have discovered that polymeric quaternary ammonium salts of those classes, when formulated in an aqueous medium with one or more nonionic surfactants, provide stable, isotropic liquid laundry detergents and sanitizer compositions having good detergency and bactericidal properties, which, in addition, are moderately irritating to the eyes and practically non-irritating to the skin.
r. Accordingly, the invention resides in stable, isotropic liquid laundry detergent and sanitizer compositions comprising: a polymeric linear quaternary ammonium salt selected from the group consisting of a poly[oxyethylene(di-loweralkyliminio)ethylene(di-lower-alkyliminio)ethylene dihalide] and a polymeric quaternary ammonium halide corresponding to formula IB hereinbelow; one or more nonionic surfactants selected from the group consisting of the polyethylene glycol long chain alkyl ether, polyethylene glyccl alkylphenyl ether, N-alkyl-N,N-di-lower-alkylamine-N-oxide and alkyl polyglycoside classes; and water.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS 15 More specifically the isotropic liquid laundry detergent and sanitizer compositions of the invention comprises: a polymeric linear quaternary ammonium salt which is a compound having the formula:
SR
1
R
1 a
IA
i ii ,o R 1 is lower-alkyl having from one to four 0 carbon atoms, a is an integer from 4 to 40 and I 30 X is halide; or a compound having the formula: 3I AY 4 0 AM9Ct -6- (R )3N-C 2CHCHC 2-N-H C=CHCH 2 i-N-(R 2 3 (b+2)X b 1 1B where R 2 is hydroxy-lower-alkyl having from two to four carbon atoms, b is an integer from 27 to 57 and Rand X have the meanings given above; 0 1 o~ one or more nonionic surfactants, said 0 nonionic surfactant being a compound having the formula: 0 0000 0 04 00.0 0 where R is C 8-C 9 alkyl and c is an integer from 5 to 15, o a compound having the formula: 0400 0 0 00 where 12isC-C lkyl an0 sa nee 0I -7where R 1 has the meaning given above, and an alkyl polyglycoside; and water.
The polymeric quaternary ammonium salts of formulas IA and IB used to prepare the compositions of the invention are well known classes of compounds. The poly[oxyethylene(di-lower-alkyliminio)ethylene(di-lower-alkyliminio)ethylene dihalide] quaternaries of formula IA include, for example, poly[oxyethylene(dimethyliminio)ethylene(dimethyliminio)ethylene dichloride] sold under the trade name i BUSAN® 77 by Buckman Laboratories, Memphis, Tennessee as a 60% active solution in water and which is identified as WSCP (water soluble cationic i, S 15 polymer).
The polymeric quaternary ammonium halides of formula IB include, for example, poly(dimethylbutenyl am- I monium chloride)-c,w-bis triethanolammonium chloride I (as named by the manufacturer) sold under the trade names ONYXSPERSE® 12S and ONAMER® M by the Onyx Chemical i i 3 /r^ S--8- Company, Jersey City, New Jersey, now owned by The Stepan Company, Northfield, Illinois. ONYXSPERSE* and ONAMER* are aqueous solutions of the salt each containing, respectively, 28.5% and 29.5% actives and 12% and 1% sodium chloride respectively.
The nonionic surfactants of formulas IIA, IIB and IIC and the nonionic alkyl polyglyc6side surfactants used in the practice of the present invention are well 4 I known in commerce. Examples of the polyethylene glycol 8' 10 long chain alkyl ethers of formula IIA are sold under the Union Carbide (Danbury, Connecticut) trade name TERGITOL* i or the Shel Chemical Company (Houston, Texas) trade name NEODOL* and are identified by the CTFA adopted name, Si pareth. Suitable members of the group for the practice of the present invention are pareth-15-5, pareth-15-7, pareth-15-9, pareth-15-12, pareth-23-7, pareth-25-5, pareth-25-7, pareth-25-9, pareth-25-12, pareth-45-7, pareth-45-11 and pareth-45-13, where the first given numbers 15, 23, 25 and 45 indicate R 4 alkyl chain lengths from 11 to 15, 12 to 13, .1.2 to 15 and 14 to 15 carbon atoms, respectively, and the second given numbers 7, 9, 11, 12 and 13 indicate the average number of ethyleneoxy groups, i The polyethylene glycol alkyl phenyl ethers of formula IIB are available, for example, under the Rohm and Haas (Philadelphia, Pennsylvania) trade names TRITON* X and TRITON* N or the GAF Corporation (Wayne, New Jersey) trade names IGEPAL* CA and IGEPAL* CO and are identified by the CTFA adopted names of octoxynols and nonoxynols.
-9- These include, for example, octoxynol-7, and octoxynol-13, where R 5 in formula IIB is C 8 alkyl and d has an average value of 7, 10 and 13, respectively, and nonoxynol-7, nonoxynol-8, nonoxynol-9 and nonoxynol- 13, etc. where R in formula IIB is C alkyl, and d has an average value of 7, 8, 9 and 13, respectively.
I The alkylamine oxides of formula IIC are sold under the trade name AMMONYX* by the Onyx Chemical Company (Jersey City, New Jersey) and include, for example, 10 lauramine oxide, myristylamine oxide, palmitamine oxide S [and stearamine oxide which are the CTFA adopted names for the compounds of formula IIC where R 1 in each in- 1 f stance is methyl and the alkyl group has 12, 14, 16 and 18 carbon atoms respectively.
V 15 The nonionic alkyl polyglycoside surfactants are sold by Staley Industrial Products of the A. E. Staley ij t Manufacturing Company (Decatur, Illinois) and include, for example, APG-23-3 which is a surfactant of the alkyl I polyglycoside class having an alkyl chain derived from a C 1
-C
13 straight chain alcohol and an average of 3 glucose units in the polyglycoside moiety.
Although it is preferred in the practice of the present invention to include either one or the other of the polymeric quaternary ammonium salts represented by formulas IA and IB, it is also contemplated that mixtures of salts of those two structural types can, if desired, be used in the liquid laundry detergent formulations of the invention.
The compositions of the invention contain from about 5.5 to about 20 weight percent of the polymeric quaternary ammonium salt of formulas IA or IB and from about
_II__
I to about 50 weight percent of the nonionic surfactant, all amounts being based on total weight of the composition. Preferred ranges are from about 5 to about weight percent of the polymeric quaternary salt and from about 5 to about 17 weight percent of the nonionic surfactant, and particularly preferred amounts are about 5,5 to about weight percent of the polymeric quaternary salt and from about 7 to about 12 weight percent of the nonionic surfactant.
i 't The compositions may, in order to provide addi- I 10 tional benefits, optionally contain nonessential ingred- I Sents such as fragrances, dyes, pH adjusters such as triethylamine, brighteners, solvents such as eth- Sanol, and thickeners. Generally fragrances may be used I in amounts up to about 0.7 weight percent, dyes in amounts S 15 up to about 0.02 weight percent, pH adjusters in amounts i up to about 4 weight percent, brighteners in amounts up to about 0.5 weight percent, ethanol in amounts up to about 7 weight percent, and thickeners in amounts i i up to about 2.0 weight percent.
The compositions are prepared by addition to water, wi.th stirring and heating as necessary, of the nonionic V surfactant(s), followed by alcohol if desired, followed by the polymeric quaternary ammonium salt, followed by the S, dyes, fragrances, brighten pH adjusters or thickeners, stirring being continued at each stage to effect complete solution or homogeneous dispersion.
The compositions of 'the invention possess very good detergency and bactericidal properties and furthermore have very low eye and skin irritancy. They are therefore particularly valuable in household sanitizing 1 -1- 1 j and cleaning operations where such properties are desircleaners.
The manner and process of making and using the invention, and the best mode contemplated by the inventors for carrying out the invention, will now be described so as to enable any person skilled in the art to which C r C L it pertains to make and to use the same.
EXAMPLES i c 10 A number of formulations, composed as indicated }I C.
j c in Table 1, each containing a quaternary ammonium saltj and at least one nonionic surfactant were prepared using the procedure described above. 1 Formulations A-K, each containing a polymeric quaternary of formulas IA or IB and one or more nonionic S' surfactants of formulas IIA, IIB or IIC or an alkyl poly- S° glycoside, are formulated in accordance with the inven- -tion as described above and are within the ambit of the i invention, whereas formulations L-0, each containing a monomeric quaternary halide i.e. CYNCAL* 80, and a nonionic surfactant, were prepared for comparative pur-
I
\poses and are outside the scope of the invention.
C I n In, ~I bo
I
Ingredient ONAMER* 1M (29.5) ONYXSPERSEO 12S (28.5%) BUSANO 77 (60%) CYNCALIO 80 (80%) pareth-23-7 pareth-45-7 0 TERGITOL-24-L-98 NMW pareth-15-12 pareth-15-9 nonoxynol-9 AKONYX* LO APG 23-3 (46%) Table 1 Formulation (Amts. in weight of actives) A B c D E F G -H I J K L M- N 0 6.4 6 5.5 6 6 6 6 5.5 5.5 6.4 6.4 6.4 6.4 6.4 12 5 3,7 12 12 12 12 12 10 9 10 9 5 5 8.3 2.6 2 3 7 2.6 7 5 E tOH Dye, fragrance, water
I
0 '1 0 0 P 0 I 0. 0 0 0 00.. 400 I, non I~3 Ill o Lfl 0 0 c 91 p.' 0) 0 0 0 f &A 9 0 2 ret P%1b 9 1 1 a' -13- The formulations of the invention and the comparative formulations were tested for cleaning efficacy using the standard EMPA and Krefeld detergency tests; for germicidal activity against K. pneumoniae ATCC 4352 and S. aureus ATCC 6538 using the EPA-approved Petrocci- Clark test procedure (Proposed Test Method for Antimicrobial Laundry Additives, Petrocci and Clark, J. Ass.
Offic. Anal. Chem. 52(4), 836-842 (1969)] which is a simulated in-use test method (see EPA Publication DIS/TSS- 13, May 2, 1979); for eye irritation in rabbits using the standard FIFRA method (described at 40 C.F.R. 163.81and for Skin irritation using the standard FIFRA dermal irritation test in rabbits (NAS 1138 modification described at 40 C.F.R. 163.81-5).
The EMPA and Krefeld detergency tests used in the present study are described in U.S. Patent 4,576,729 except that the temperature of the wash and rinse water was 105°F instead of 120°-130 0 F. In the EMPA test (a test by the Swiss Federal Testing Station in Switzerland), the standard soil is an India ink and olive oil emollient (an oily type soil), and in the Krefeld test (a test by the Wascherei Forschungs Institute of Krefeld, West Germany), the soil is 84% clay, 8% lamp black, 4% black 4. iron oxide and 2% yellow iron oxide oversprayed with a solution of 3.4% lanolirn dissolved in carbon tetrachloride and salt solution (the salt to resemble human perspiration). The cleaning efficacy, expressed as Soil Removal, was calculated in each test procedure for the test swatches as follows, the values obtained for any given detergent formulation being the average of the individual values so determined: i -14- R R Soil Removal x 100 SRo Rs where: R Average reflectance of washed soiled cloths
R
s Average reflectance of unwashed soiled cloths R Average reflectance of unsoiled cloths before washing Thus the higher the'value for Soil Removal, the greater the detergency.
In the germicidal activity test, EPA protocols require a germ reduction of at least 99.96% for laundry sanitizers against the two test organisms, K. pneumoniae and S. aureue.
1 "t Eye irritation results are expressed in terms Sof Draize scores in accordance with the standard FIFRA
;I
method.
t Skin irritation scores are expressed in terms 1 15 of Primary Irritation Index also in accordance Iwith the standard FIFRA method. The lower the score thus obtained, the less irritating is the formulation.
The results obtained are set forth in Tables 2, 3 and 4 where EMPA and Krefeld detergency results are expressed in terms of soil removal values; the antimicrobial activity is expressed in terms of percent germ reduction and antimicrobial effectiveness based on the abovenoted EPA protocols; eye irritation is expressed in terms of Draize scores; and skin irritation is expressed as P.I.I. values.
Table 2 (EMPA/Krefeld Detergency) Formulation
A
C
D
L
M
N
EMPA
35 36.4 36 27. 0 22.8 26 Krefeld 43 40.6 9.2 7.*9.
C C Formula
A
B
C
L
M
N
0 Table 3 (Antimicrobial Activt~Eyvs. K. pneumoniae and S..aureus) tion Germ Reduction Sanitizal 99.9 Effe 99.9 Effe 99.9 Effe 99.9 Effe 99.9 Effe 99.9 Effe 99.7 Not tlon Result -ti ve -tive .tive :tive ctive :tive Effective C' C.
Ct Formulation
A
Table 4 (Irritancy Scores) Eye Irritancy (Highest mean Draize Score) 16.3 (unwashed) 7.7 (washed) Skin Ir~ritancy I. I 0.71 73 (unwashed) 58 (washed) 2.78 -16- These results show that formulations A, C and D prepared in accordance with the invention are markedly superior in detergency properties, as determined in both EMPA and Krefeld detergency tests, to any of comparative formulations L, M and N. Formulations A, B and C are also shown to be equally or more effective in antimicrobial activity to comparative formulations L, M, N and 0 and Formulation A is shown to have lower eye and skin Sirritancy than comparative formulation N.
S' 0The liquid laundry detergent formulations of S the invention are formulated as concentrates. In use the concentrate is added to the wash water in such amounts as to provide good cleaning and sanitization. It has j been found that about 1/2 cup (about 4 ounces) of concentrate per wash 3lad (or about 4 ounces per 16 gallons), j which provides a use dilution of around 1:500, is adequate to achieve such purposes.
'i
Claims (2)
1. A liquid laundry detergent and sanitizing composition comprising: a polymeric linear quaternary ammonium salt which is a compound having the formula: 2X wherein Id C C, CT C, SC CI I C R 1 is lower-alkyl having from one to four carbon atoms, a is an integer from 4 to 40 and X is halidej or a compound having the formula: R I (R2) 3 N-CH 2 CH=CHCH 2 N-CCHC=CHCH2 N-(R 2 3 (b+2)X 20 I RI b IB 2 where R 2 is hydroxy-lower-alkyl having from two to four carbon atoms, b is an integer from 27 to 57 and R1 and X- have the meanings given above; one or more nonionic surfactants, said nonionic surfactant being a compound having the formula: R 4 (OCH 2 CH 2 )OH IIA c L, -18- where R 4 is C 1 1 -C 1 5 alkyl and c is an integer from 5 to 15, a compound having the formula: R 5 *--(0OCH 2 CH2)dOH IIB where R5 is C 8 -C 9 alkyl and d is an integer from 7 to 13, or a compound having the formula: C 12 -C 18 Alkyl N 0 1 IIC
15. where R 1 has the meaning given above, and an alkyl polyglycoside; and water. 2. A composition according'to'laim 1, wherein I .t the quaternary ammonium salt is a compound of formula IA. 3. A composition according to claim 1, wherein aIt the quaternary ammonium salt is a compound of formula IB. 4. A composition according to any one of the preceding claims, containing from 5.5 to 20 weight percent of the quaternary ammonium salt and from 5 to weight percent of the nonionic surfactant. 5. A composition according to claim 4, which contains from 5.5 to 10 weight percent of the quaternary ammonium salt and from 5 to 17 weight percent of the nonionic surfactant. 6. A composition according to any one of the preceding claims, which contains a nonionic surfactant of formula IIA. -19- 7. A composition according to any one of the preceding claims, which contains a mixture of nonionic surfactants of formulas IIA and IIC. 8. A composition according to claim 1, contain- ing 6 weight percent of poly[oxyethylene(dimethyl- imino)ethylene (dimethyliminio)ethylene dichloride] and 12 weight percent of pareth-45-7. 9. A composition according to claim 1, contain- ing 6 weight percent of poly(dimethyl butenyl ammon- ium chloride)-a,ow-bis-triethanolammonium chloride and 12 weight percent of pareth-45-7. A composition according to claims 6 or 9, which includes up to 7 weight percent of ethanol. 11. A liquid laundry detergent and sanitizing o" 15 composition substantially as herein described with reference to any one of the Examples. 12. A liquid laundry detergent and sanitizing composition substantially as herein described. 13. A liquid laundry detergent and sanitizing 20 composition as defined in claim 1 substantially as I herein described with reference to any one of the Examples. DATED this TWENTY-EIGHTH day of AUGUST 1990 ,25 Sterling Drug Inc. Patent Attorneys for the Applicant SPRUSON FERGUSON /i
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/935,658 US4755327A (en) | 1986-11-26 | 1986-11-26 | Isotropic laundry detergents containing polymeric quaternary ammonium salts |
| US935658 | 1986-11-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU8139687A AU8139687A (en) | 1988-06-02 |
| AU604275B2 true AU604275B2 (en) | 1990-12-13 |
Family
ID=25467479
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU81396/87A Ceased AU604275B2 (en) | 1986-11-26 | 1987-11-19 | Isotropic laundry detergents containing polymeric quaternary ammonium salts |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS63150388A (en) |
| AU (1) | AU604275B2 (en) |
| CA (1) | CA1301584C (en) |
| NZ (1) | NZ222291A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL90554A0 (en) * | 1988-06-29 | 1990-01-18 | Sterling Drug Inc | Compositions containing preservative systems and nonwoven wipes impregnated therewith |
| JP4512246B2 (en) * | 2000-09-11 | 2010-07-28 | 株式会社日立製作所 | Operation instruction method for inspection equipment |
-
1987
- 1987-10-20 CA CA000549702A patent/CA1301584C/en not_active Expired - Lifetime
- 1987-10-23 NZ NZ22229187A patent/NZ222291A/en unknown
- 1987-11-19 AU AU81396/87A patent/AU604275B2/en not_active Ceased
- 1987-11-20 JP JP29386387A patent/JPS63150388A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU8139687A (en) | 1988-06-02 |
| JPS63150388A (en) | 1988-06-23 |
| NZ222291A (en) | 1990-04-26 |
| CA1301584C (en) | 1992-05-26 |
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