NO132674B - - Google Patents

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Info

Publication number: NO132674B
Authority: NO; Norway
Prior art keywords: acid; weight; parts; mol; preparation
Prior art date: 1970-02-27

Application number

NO101/71A

Other languages

English (en)

Norwegian (no)

Other versions

NO132674C (da

Inventor

E Hofmann

U Holtschmidt

Original Assignee

Goldschmidt Ag Th

Priority date (The priority date 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 date listed.)

1970-02-27

Filing date

1971-01-12

Publication date

1975-09-08

1970-02-27 Priority claimed from DE19702009276 external-priority patent/DE2009276C/de

1971-01-12 Application filed by Goldschmidt Ag Th filed Critical Goldschmidt Ag Th

1975-09-08 Publication of NO132674B publication Critical patent/NO132674B/no

1975-12-17 Publication of NO132674C publication Critical patent/NO132674C/no

Links

238000002360 preparation method Methods 0.000 claims abstract description 24
230000000844 anti-bacterial effect Effects 0.000 claims abstract description 9
150000001875 compounds Chemical class 0.000 claims description 24
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 21
239000002253 acid Substances 0.000 claims description 9
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 8
RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 4
239000004310 lactic acid Substances 0.000 claims description 4
235000014655 lactic acid Nutrition 0.000 claims description 4
239000011975 tartaric acid Substances 0.000 claims description 4
235000002906 tartaric acid Nutrition 0.000 claims description 4
RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 claims description 3
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
235000011054 acetic acid Nutrition 0.000 claims description 3
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
235000015165 citric acid Nutrition 0.000 claims description 3
239000000174 gluconic acid Substances 0.000 claims description 3
235000012208 gluconic acid Nutrition 0.000 claims description 3
235000011167 hydrochloric acid Nutrition 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
229910017604 nitric acid Inorganic materials 0.000 claims description 3
235000011007 phosphoric acid Nutrition 0.000 claims description 3
230000000721 bacterilogical effect Effects 0.000 description 12
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
OXWFFWJKUNMMSO-UHFFFAOYSA-N n-octyl-n'-[2-(octylamino)ethyl]ethane-1,2-diamine Chemical compound CCCCCCCCNCCNCCNCCCCCCCC OXWFFWJKUNMMSO-UHFFFAOYSA-N 0.000 description 6
239000002736 nonionic surfactant Substances 0.000 description 6
239000000047 product Substances 0.000 description 6
239000000344 soap Substances 0.000 description 6
229910001868 water Inorganic materials 0.000 description 6
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 5
239000013543 active substance Substances 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
238000005187 foaming Methods 0.000 description 5
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 4
239000003599 detergent Substances 0.000 description 4
235000014103 egg white Nutrition 0.000 description 4
210000000969 egg white Anatomy 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
150000003856 quaternary ammonium compounds Chemical class 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 3
102000002322 Egg Proteins Human genes 0.000 description 3
108010000912 Egg Proteins Proteins 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 description 2
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
239000000370 acceptor Substances 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
230000001580 bacterial effect Effects 0.000 description 2
239000000872 buffer Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000006260 foam Substances 0.000 description 2
238000011068 loading method Methods 0.000 description 2
NAPBLZKQMLMWHK-UHFFFAOYSA-N n'-(2-aminoethyl)-n'-octylethane-1,2-diamine Chemical compound CCCCCCCCN(CCN)CCN NAPBLZKQMLMWHK-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
238000003756 stirring Methods 0.000 description 2
VMKOFRJSULQZRM-UHFFFAOYSA-N 1-bromooctane Chemical compound CCCCCCCCBr VMKOFRJSULQZRM-UHFFFAOYSA-N 0.000 description 1
RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
ORTUYCUWCKNIND-UHFFFAOYSA-N 3-[2-(2-aminoethylamino)ethylamino]propanenitrile Chemical compound NCCNCCNCCC#N ORTUYCUWCKNIND-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
239000005083 Zinc sulfide Substances 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000003619 algicide Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
238000003975 animal breeding Methods 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
238000003287 bathing Methods 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
235000013365 dairy product Nutrition 0.000 description 1
230000007547 defect Effects 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
OOZFJMRPUVMHEW-UHFFFAOYSA-N dioctyl sulfate Chemical compound CCCCCCCCOS(=O)(=O)OCCCCCCCC OOZFJMRPUVMHEW-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 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 description 1
238000000921 elemental analysis Methods 0.000 description 1
235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
-1 glycol ethers Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
229920003087 methylethyl cellulose Polymers 0.000 description 1
239000000203 mixture Substances 0.000 description 1
RZRNAYUHWVFMIP-UHFFFAOYSA-N monoelaidin Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-UHFFFAOYSA-N 0.000 description 1
BRNPMBFYMPUNSK-UHFFFAOYSA-N n'-(2-aminoethyl)-n'-dodecylethane-1,2-diamine Chemical compound CCCCCCCCCCCCN(CCN)CCN BRNPMBFYMPUNSK-UHFFFAOYSA-N 0.000 description 1
NZTZKCVOQYVLDO-UHFFFAOYSA-N n'-[2-(didodecylamino)ethyl]ethane-1,2-diamine Chemical compound CCCCCCCCCCCCN(CCNCCN)CCCCCCCCCCCC NZTZKCVOQYVLDO-UHFFFAOYSA-N 0.000 description 1
RRHLGOOTLYHTEW-UHFFFAOYSA-N n'-[2-(dodecylamino)ethyl]ethane-1,2-diamine Chemical class CCCCCCCCCCCCNCCNCCN RRHLGOOTLYHTEW-UHFFFAOYSA-N 0.000 description 1
YBUMEUMBIWOBBF-UHFFFAOYSA-N n'-[2-(octylamino)ethyl]ethane-1,2-diamine Chemical compound CCCCCCCCNCCNCCN YBUMEUMBIWOBBF-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
235000014214 soft drink Nutrition 0.000 description 1
229960004793 sucrose Drugs 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms

Landscapes

Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

NO10171A 1970-02-27 1971-01-12 NO132674C (da)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19702009276 DE2009276C (de)		1970-02-27	Biocide

Publications (2)

Publication Number	Publication Date
NO132674B true NO132674B (da)	1975-09-08
NO132674C NO132674C (da)	1975-12-17

Family

ID=5763570

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO10171A NO132674C (da)	1970-02-27	1971-01-12

Country Status (12)

Country	Link
JP (1)	JPS5336010B1 (da)
AT (1)	AT303269B (da)
BE (1)	BE761318A (da)
CH (1)	CH534480A (da)
DK (1)	DK137707C (da)
ES (1)	ES388822A1 (da)
FR (1)	FR2080797B1 (da)
GB (1)	GB1300694A (da)
IT (1)	IT1008004B (da)
NL (1)	NL142316B (da)
NO (1)	NO132674C (da)
SE (1)	SE362585B (da)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4048324A (en) *	1973-12-28	1977-09-13	Armand Kohn	Fungicidal composition and method
FR2471192A1 (fr) *	1979-12-13	1981-06-19	Corning Glass Works	Procede de desinfection de reacteurs a enzymes immobilises
JP3356289B2 (ja) *	1995-06-26	2002-12-16	コンキャットリミティド	第一遷移系列元素に対してキレート化親和性および選択性のある化合物とその医療および診断への使用
WO2001000024A1 (de) *	1999-06-25	2001-01-04	Lonza Ag	Desinfektionsmittel

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2244712A (en) *	1939-12-04	1941-06-10	Monsanto Chemicals	Control of ambrosia beetles

1970
- 1970-12-14 CH CH1849770A patent/CH534480A/de not_active IP Right Cessation
- 1970-12-16 SE SE1705270A patent/SE362585B/xx unknown
- 1970-12-17 AT AT1138770A patent/AT303269B/de not_active IP Right Cessation
- 1970-12-24 FR FR7046638A patent/FR2080797B1/fr not_active Expired
- 1970-12-28 JP JP13080470A patent/JPS5336010B1/ja active Pending
- 1970-12-28 DK DK658270A patent/DK137707C/da active
1971
- 1971-01-02 IT IT4750771A patent/IT1008004B/it active
- 1971-01-07 BE BE761318A patent/BE761318A/xx not_active IP Right Cessation
- 1971-01-12 NO NO10171A patent/NO132674C/no unknown
- 1971-01-14 NL NL7100500A patent/NL142316B/xx not_active IP Right Cessation
- 1971-02-20 ES ES388822A patent/ES388822A1/es not_active Expired
- 1971-04-19 GB GB2228771A patent/GB1300694A/en not_active Expired

Also Published As

Publication number	Publication date
NL7100500A (da)	1971-08-31
AT303269B (de)	1972-11-27
NL142316B (nl)	1974-06-17
IT1008004B (it)	1976-11-10
BE761318A (fr)	1971-06-16
DE2009276A1 (da)	1971-05-13
FR2080797A1 (da)	1971-11-19
NO132674C (da)	1975-12-17
DK137707C (da)	1978-10-02
FR2080797B1 (da)	1973-12-28
JPS5336010B1 (da)	1978-09-30
SE362585B (da)	1973-12-17
CH534480A (de)	1973-03-15
GB1300694A (en)	1972-12-20
ES388822A1 (es)	1973-05-16
DK137707B (da)	1978-04-24

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GB930296A (en)	1963-07-03	The preparation of acylamino compounds
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US3733420A (en)	1973-05-15	Biocidal octyldodecyl dimethyl ammonium compounds in hard water solutions
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JPS5854074A (ja)	1983-03-30	洗たく用ソフトリンス剤
US2871091A (en)	1959-01-27	Method of disinfecting
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