DE1228031B - Bakterizide - Google Patents
BakterizideInfo
- Publication number
- DE1228031B DE1228031B DEF46300A DEF0046300A DE1228031B DE 1228031 B DE1228031 B DE 1228031B DE F46300 A DEF46300 A DE F46300A DE F0046300 A DEF0046300 A DE F0046300A DE 1228031 B DE1228031 B DE 1228031B
- Authority
- DE
- Germany
- Prior art keywords
- phosphorus pentoxide
- products
- condensation
- mono
- carbon atoms
- 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.)
- Pending
Links
- 230000000844 anti-bacterial effect Effects 0.000 title claims description 7
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 24
- 239000000047 product Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000007859 condensation product Substances 0.000 claims description 5
- 229920000137 polyphosphoric acid Polymers 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 150000001983 dialkylethers Chemical class 0.000 claims description 4
- 239000003899 bactericide agent Substances 0.000 claims description 2
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 claims 2
- 150000003014 phosphoric acid esters Chemical class 0.000 claims 2
- -1 alkyl phosphates Chemical class 0.000 description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 4
- 235000011007 phosphoric acid Nutrition 0.000 description 4
- 150000003016 phosphoric acids Chemical class 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229950011008 tetrachloroethylene Drugs 0.000 description 2
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 1
- QHXGRVYSGODPIC-UHFFFAOYSA-N 6,6-diethyloctyl dihydrogen phosphite Chemical compound CCC(CC)(CC)CCCCCOP(O)O QHXGRVYSGODPIC-UHFFFAOYSA-N 0.000 description 1
- BUADUHVXMFJVLH-UHFFFAOYSA-N 7-chloro-3-imidazol-1-yl-2H-1,2,4-benzotriazin-1-ium 1-oxide Chemical compound N1[N+](=O)C2=CC(Cl)=CC=C2N=C1N1C=CN=C1 BUADUHVXMFJVLH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 241000588767 Proteus vulgaris Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- PAZHOQPRMVOBDD-RMRYJAPISA-N cyclopenta-1,3-diene;(1s)-1-(2-diphenylphosphanylcyclopenta-1,4-dien-1-yl)-n,n-dimethylethanamine;iron(2+) Chemical compound [Fe+2].C=1C=C[CH-]C=1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1[C@@H](N(C)C)C PAZHOQPRMVOBDD-RMRYJAPISA-N 0.000 description 1
- 238000004090 dissolution 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
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- QXLBKTGZGPVJOO-UHFFFAOYSA-N hexyl dihydrogen phosphite Chemical compound CCCCCCOP(O)O QXLBKTGZGPVJOO-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 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
- 238000002360 preparation method Methods 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- XTTGYFREQJCEML-UHFFFAOYSA-N tributyl phosphite Chemical compound CCCCOP(OCCCC)OCCCC XTTGYFREQJCEML-UHFFFAOYSA-N 0.000 description 1
- OHRVKCZTBPSUIK-UHFFFAOYSA-N tridodecyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCC)OCCCCCCCCCCCC OHRVKCZTBPSUIK-UHFFFAOYSA-N 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- SFENPMLASUEABX-UHFFFAOYSA-N trihexyl phosphate Chemical compound CCCCCCOP(=O)(OCCCCCC)OCCCCCC SFENPMLASUEABX-UHFFFAOYSA-N 0.000 description 1
- DECPGQLXYYCNEZ-UHFFFAOYSA-N tris(6-methylheptyl) phosphite Chemical compound CC(C)CCCCCOP(OCCCCCC(C)C)OCCCCCC(C)C DECPGQLXYYCNEZ-UHFFFAOYSA-N 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/098—Esters of polyphosphoric acids or anhydrides
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF46300A DE1228031B (de) | 1965-06-11 | 1965-06-11 | Bakterizide |
LU51194D LU51194A1 (da) | 1965-06-11 | 1966-05-26 | |
NL6607823A NL6607823A (da) | 1965-06-11 | 1966-06-06 | |
SE794166A SE319579B (da) | 1965-06-11 | 1966-06-10 | |
FR1490608D FR1490608A (fr) | 1965-06-11 | 1966-06-10 | Nouveaux bactéricides |
DK301466A DK113515B (da) | 1965-06-11 | 1966-06-10 | Desinfektions- eller konserveringsmiddel. |
BE682445D BE682445A (da) | 1965-06-11 | 1966-06-13 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF46300A DE1228031B (de) | 1965-06-11 | 1965-06-11 | Bakterizide |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1228031B true DE1228031B (de) | 1966-11-03 |
Family
ID=7100956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF46300A Pending DE1228031B (de) | 1965-06-11 | 1965-06-11 | Bakterizide |
Country Status (7)
Country | Link |
---|---|
BE (1) | BE682445A (da) |
DE (1) | DE1228031B (da) |
DK (1) | DK113515B (da) |
FR (1) | FR1490608A (da) |
LU (1) | LU51194A1 (da) |
NL (1) | NL6607823A (da) |
SE (1) | SE319579B (da) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0197128A1 (en) * | 1984-10-09 | 1986-10-15 | Interface Res Corp | MICROBICIDE COMPOSITION AND PROCESS FOR PREPARING THE SAME. |
US4908209A (en) | 1983-08-16 | 1990-03-13 | Interface, Inc. | Biocidal delivery system of phosphate ester and method of preparation thereof |
US4935232A (en) * | 1983-08-16 | 1990-06-19 | Interface Research Corporation | Microbiocidal composition and method of preparation thereof |
US4957948A (en) * | 1988-05-05 | 1990-09-18 | Interface, Inc. | Biocidal protective coating for heat exchanger coils |
US5024840A (en) * | 1984-03-08 | 1991-06-18 | Interface, Inc. | Antimicrobial carpet and carpet tile |
US5032310A (en) * | 1983-08-16 | 1991-07-16 | Interface, Inc. | Microbiocidal cleansing and disinfecting formulations and preparation thereof |
US5133933A (en) | 1983-08-16 | 1992-07-28 | Interface Research Corporation | Microbiocidal preservative |
US5474739A (en) | 1978-02-04 | 1995-12-12 | Interface, Inc. | Microbiocidal composition |
US5635192A (en) | 1988-05-05 | 1997-06-03 | Interface, Inc. | Biocidal polymeric coating for heat exchanger coils |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2402703A (en) * | 1942-08-06 | 1946-06-25 | Victor Chemical Works | Method of producing neutral esters of molecularly dehydrated phosphoric acids |
-
1965
- 1965-06-11 DE DEF46300A patent/DE1228031B/de active Pending
-
1966
- 1966-05-26 LU LU51194D patent/LU51194A1/xx unknown
- 1966-06-06 NL NL6607823A patent/NL6607823A/xx unknown
- 1966-06-10 DK DK301466A patent/DK113515B/da unknown
- 1966-06-10 SE SE794166A patent/SE319579B/xx unknown
- 1966-06-10 FR FR1490608D patent/FR1490608A/fr not_active Expired
- 1966-06-13 BE BE682445D patent/BE682445A/xx unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2402703A (en) * | 1942-08-06 | 1946-06-25 | Victor Chemical Works | Method of producing neutral esters of molecularly dehydrated phosphoric acids |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5474739A (en) | 1978-02-04 | 1995-12-12 | Interface, Inc. | Microbiocidal composition |
US4908209A (en) | 1983-08-16 | 1990-03-13 | Interface, Inc. | Biocidal delivery system of phosphate ester and method of preparation thereof |
US4935232A (en) * | 1983-08-16 | 1990-06-19 | Interface Research Corporation | Microbiocidal composition and method of preparation thereof |
US5032310A (en) * | 1983-08-16 | 1991-07-16 | Interface, Inc. | Microbiocidal cleansing and disinfecting formulations and preparation thereof |
US5133933A (en) | 1983-08-16 | 1992-07-28 | Interface Research Corporation | Microbiocidal preservative |
US5024840A (en) * | 1984-03-08 | 1991-06-18 | Interface, Inc. | Antimicrobial carpet and carpet tile |
EP0197128A1 (en) * | 1984-10-09 | 1986-10-15 | Interface Res Corp | MICROBICIDE COMPOSITION AND PROCESS FOR PREPARING THE SAME. |
EP0197128A4 (en) * | 1984-10-09 | 1989-07-25 | Interface Res Corp | MICROBICIDE COMPOSITION AND PROCESS FOR PREPARING THE SAME. |
US4957948A (en) * | 1988-05-05 | 1990-09-18 | Interface, Inc. | Biocidal protective coating for heat exchanger coils |
US5635192A (en) | 1988-05-05 | 1997-06-03 | Interface, Inc. | Biocidal polymeric coating for heat exchanger coils |
US5639464A (en) | 1988-05-05 | 1997-06-17 | Interface, Inc. | Biocidal polymeric coating for heat exchanger coils |
Also Published As
Publication number | Publication date |
---|---|
NL6607823A (da) | 1966-12-12 |
LU51194A1 (da) | 1968-02-21 |
SE319579B (da) | 1970-01-19 |
FR1490608A (fr) | 1967-08-04 |
DK113515B (da) | 1969-03-31 |
BE682445A (da) | 1966-12-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1445949C3 (de) | O,O Dialkyl pynd 6 yl phosphor säureester. Verfahren zur Herstellung derselben und ihre Verwendung | |
DE1296139B (de) | Verfahren zur Herstellung von komplexen, salzartigen Molybdaenoxyd-Schwefel-Dithiophosphorsaeure-O, O-diestern | |
DE1246730B (de) | Verfahren zur Herstellung von Amidothiol-phosphorsaeure-O-methyl-S-methyl-ester | |
DE1228031B (de) | Bakterizide | |
DE1206425B (de) | Verfahren zur Herstellung von Phosphorsaeureestern | |
DE1050746B (de) | Verfahren zur Herstellung von Trialkylphosphiten | |
DE2814330B2 (de) | Verfahren zur Herstellung von 2,6-Dichlorpyridin-Derivaten | |
DE2166270C3 (de) | Nicotinoylaminoäthansulfonyl-2amino-thiazol | |
DE1231244C2 (de) | Verfahren zur Herstellung von Estern, Esteramiden oder Amiden der Pyrophosphorsaeureoder der Unterphosphorsaeure | |
DE2160783B2 (de) | Phosphorsäureester von polyfluorierten Alkoholen | |
DE2131153A1 (de) | Wasserloesliche antibakterielle Verbindungen unterirdischer Stollen | |
DE1445659C (de) | Pyndylphosphorverbindungen und Verfahren zu ihrer Herstellung | |
DE533468C (de) | Verfahren zur Darstellung antiseptischer Mittel | |
DE948687C (de) | Verfahren zur Herstellung von Dialkylxanthinabkoemlingen | |
DE2724407C3 (de) | Verfahren zur Gewinnung von Methyldichlorphosphan | |
AT253526B (de) | Verfahren zur Herstellung neuer Phosphorsäureester | |
DE1545790C (de) | Pyrazolo-pyrimidin-thionophosphorsäuren und Verfahren zu ihrer Herstellung | |
DE947367C (de) | Verfahren zur Herstellung von O,O-Dimethyl-thiolphosphorsaeureestern | |
DE2931079C2 (de) | 1-Di-(äthylenimido)-thiophosphoryl-2-trichlormethyl-Δ↑2↑-imidazolin, dessen Herstellung und diese Verbindung enthaltende Arzneimittel | |
AT229883B (de) | Verfahren zur Herstellung von neuen Thiophosphorsäureestern | |
DE1693197C (de) | 0,0 Dialkyl S (bzw 0 ) (N alkox ymethyl) carbamoylmethyl thionophosphorsaureester und Verfahren zu ihrer Herstellung | |
DE171790C (da) | ||
DE1141277B (de) | Verfahren zur Herstellung von Phosphorsaeureestern | |
DE2053840A1 (en) | Carbamide acid chlorides/bromides prodn - by reaction of substd formamides with phosphorus-trihalides then with thionyl hal | |
DE1141989B (de) | Verfahren zur Herstellung von S-substituierten Thionothiolphosphon-oder-phosphinsaeurederivaten |