DE1228031B - Bactericidal - Google Patents
BactericidalInfo
- 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)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
BUNDESREPUBLIK DEUTSCHLANDFEDERAL REPUBLIC OF GERMANY
DEUTSCHESGERMAN
PATENTAMTPATENT OFFICE
AUSLEGESCHRIFTEDITORIAL
Int. CL:Int. CL:
A611A611
Deutsche Kl.: 3Oi-3German class: 3Oi-3
Nummer: F 46300IV a/30 iNumber: F 46300IV a / 30 i
Aktenzeichen: 1228 031File number: 1228 031
Anmeldetag: 11. Juni 1965Filing date: June 11, 1965
Auslegetag: 3. November 1966Open date: November 3, 1966
Phosphorpentoxyd setzt sich bekanntlich mit Trialkylphosphiten, Trialkylphosphäten, Mono- und Dialkylphosphorsäuren oder Dialkyläthefn um. Es wurde überraschenderweise gefunden, daß die so entstehenden Produkte eine erhebliche bakterizide Wirkung besitzen, besonders gegen gtampositive, aber auch in durchaus vertretbaren Konzentrationen gegen gramnegative Organismen. 'As is well known, phosphorus pentoxide reacts with trialkyl phosphites, trialkyl phosphates, mono- and dialkyl phosphoric acids or dialkyl ether. It was surprisingly found that so resulting products have a significant bactericidal effect, especially against gtampositive, but also in acceptable concentrations against gram-negative organisms. '
Die Herstellung der genannten Kondensationsprodükte erfolgt durch Eintragen/ der notwendigen Menge Phosphorpentoxyd zu einer Lösung der Mono- bzw. Di- bzw. Trialkylphosphite öder -alk'ylphosphate oder deren Mischungen in einem indifferenten Lösungsmittel bei relativ niederen Temperaturen. Die Umsetzungstemperatur soll üblicherweise nicht über 60°C ansteigen. Als indifferente ίοβμ^βητίΐίεί1 eignen sich beispielsweise niedermolekulare chlorierte aliphatische Kohlenwasserstoffe wie Perchloräthylen. ader .Chloroform. . The condensation products mentioned are produced by adding the necessary amount of phosphorus pentoxide to a solution of the mono-, di- or trialkyl phosphites or alkyl phosphates or mixtures thereof in an inert solvent at relatively low temperatures. The reaction temperature should usually not rise above 60.degree. As indifferent ίοβμ ^ βητίΐίεί 1 , for example, low molecular weight chlorinated aliphatic hydrocarbons such as perchlorethylene are suitable. vein .chloroform. .
Eine Richtvorschrift für die Herstellung von n-Hexylpolyphosphorsäureestern sei ^nachstehend gegeben: : ίA straightening method for the preparation of n-Hexylpolyphosphorsäureestern is given below ^:: ί
A. Zu 100 Gewichtsteilen eines Gemisches von Mono- und Dihexylphosphorsäureister (1:1) und 125 Gewichisteilen Perchloräthylen als Verdünnungsmittel werden in eineih mit Rückflußkühler und Thermometer versehenen Rührkolben unter Feuchtigkeitsausschltiß und gleichzeitigem ; gutem Rühren 25 Gewichtsjteile Phosphorpentoxyd in kleinen Portionen eingetragen. Nach beendeter Zugabe wird ι das Reaktionsgemisch dann über Nacht bei 45 bis 50° C bis zur vollständigen Auflösung ; des Phosphorpentoxyds stehengelassen. Sollten in jder Lösung etwa noch geringe Anteile von: nicht in Reaktion getretenem Phosphorpentoxyd vorhanden sein, kann die Lösung des Polyphosphorsäure-n-hexylesters zentrifugiert werden. :A. To 100 parts by weight of a mixture of mono- and dihexylphosphoric acid ester (1: 1) and 125 parts by weight of perchlorethylene as a diluent are in a row with a reflux condenser and Mixing flask provided with a thermometer with exclusion of moisture and at the same time; good stirring 25 parts by weight of phosphorus pentoxide in small portions registered. After the addition has ended, the reaction mixture is then kept at 45 to 50 ° C. overnight until complete dissolution; of phosphorus pentoxide ditched. Should there still be small amounts of: not reacted in each solution If phosphorus pentoxide is present, the solution of the polyphosphoric acid n-hexyl ester can be centrifuged will. :
B. 85 Gewichtsteile Phosphorpentoxyd werden in der vorstehend beschriebenen Apparatur unter Feuchtigkeitsausschluß bei gleichzeitigem gütern Rühren in kleinen Portionen in eine' Mischung von 200 Gewichtsteilen n-Hexylphosphit urjd 100 Gewiqhtsteilen Chloroform eingetragen. Unter starker Wärmetönung !tritt die Reaktion ein. Durch Kühlung sorgt nian dafür, daß die Temperatur des Reaktionsgemisches 5Ö°C nicht übersteigt. Sobald die Gesamtmenge · des Phosphorpentoxydes eingetragen ist, wird das Reaktionsgemisch noch weitere 2 Stunden ,auf 5O0C erwärmt, wobei alles Phosphorpentoxyd in Lösung geht. Die erhaltene Lösung wird anschließend durch einen Druckfilter filtriert und das als Verdünnungsmittel zugesetzte Chloroform bei 5O0C im Vakuum BakterizideB. 85 parts by weight of phosphorus pentoxide are entered in the apparatus described above with exclusion of moisture with simultaneous good stirring in small portions in a 'mixture of 200 parts by weight of n-hexyl phosphite urjd 100 parts by weight of chloroform. The reaction occurs with a strong warming! By cooling, Nian ensures that the temperature of the reaction mixture does not exceed 50 ° C. Once the total amount is entered · the Phosphorpentoxydes, the reaction mixture for a further 2 hours, warmed to 5O 0 C, with all phosphorus pentoxide dissolves. The solution obtained is subsequently filtered through a pressure filter and the added diluent chloroform at 5O 0 C in vacuo bactericides
Anmelder:Applicant:
Farbwerke Hoechst AktiengesellschaftFarbwerke Hoechst Aktiengesellschaft
vormals; Meister Lucius & Brüning, Frankfurt/M.formerly; Master Lucius & Brüning, Frankfurt / M.
Als Erfinder benannt:Named as inventor:
Dr. Claus Heuck,Dr. Claus Heuck,
Dr. Karl Heiriz Wallhäußer, Hofheim (Taunus) --Dr. Karl Heiriz Wallhäußer, Hofheim (Taunus) -
abdestilliert. Man erhält auf diese Weise 279 Gewichtsteile Polyphosphorsäure-n-hexylester.distilled off. In this way, 279 parts by weight are obtained Polyphosphoric acid n-hexyl ester.
Die als Lösungen in organischen Lösungsmitteln anfallenden Produkte werden üblicherweise in Form von wäßrigen Emulsionen eingesetzt. Als EmulgatorenThe products obtained as solutions in organic solvents are usually in the form used by aqueous emulsions. As emulsifiers
( . für die Herstellung dieser Emulsionen eignen sich '."', sowohl nichtionogene als auch .anionaktive oder kationaktive Emulgatoren. Soweit die Polyphosphorsäurederivate wasserlöslich sind, können sie auch ', durch Abdampfen des 'organischen Lösungsmittels ' ' isoliert werden und in gelöster. Form, d. h. in wäßriger ; Lösung, angewendet Werden. ( . For the production of these emulsions '. "' are suitable, both non-ionic and also anion-active or cation-active emulsifiers. If the polyphosphoric acid derivatives are water-soluble, they can also be isolated by evaporating the 'organic solvent' and in dissolved form , that is, in an aqueous solution.
Während die für die Herstellung der Polyphosphoric säurederivate als Ausgangsmaterial dienenden Verbindungen, wie z. B. Dialkyläther, Trialkylphosphate, .:< Trialkylphosphite sowie die diesen entsprechenden '! Mono- und Dialkylphosphorsäuren, keine nennenswerte antimikrobielle Wirksamkeit aufweisen, zeigen die Kondensationsprodukte, die mit Phosphorpentoxyd erhalten werden, in Abhängigkeit von der Kettenlänge der Alkylreste eine Zunahme der bakteriziden Wirksamkeit mit zunehmender Kettenlänge, wobei ein Optimum der Wirkung bei AJkylresten mit Kettenlängen von etwa 4 bis etwa 12 Kohlenstoffatomen erreicht wird. Am ausgeprägtesten ist die Wirkung bei Verbindungen, deren Alkylreste eine Kohlenstoff ketteWhile those used for making the Polyphosphoric acid derivatives serving as starting material compounds, such as. B. dialkyl ethers, trialkyl phosphates, .: <Trialkyl phosphites and the corresponding '! Mono- and dialkyl phosphoric acids, none noteworthy Have antimicrobial effectiveness, show the condensation products with phosphorus pentoxide be obtained, depending on the chain length of the alkyl radicals, an increase in the bactericidal effectiveness with increasing chain length, with an optimum effect in the case of alkyl residues with chain lengths from about 4 to about 12 carbon atoms is achieved. The effect is most pronounced at Compounds whose alkyl radicals form a carbon chain
;' von 6 bis 8 Kohlenstoffatomen tragen, wobei zu berücksichtigen ist, daß die optimale Wirksamkeit weitgehend von den gestellten Forderungen, wie z.B. der Löslichkeit der Stabilität usw., abhängig ist. Ein Teil der Verbindungen ist auf Grund seiner Löslichkeit und bakteriziden Wirksamkeit in einer Reihe von organischen Lösungsmitteln von besonderem Interesse. Die minimale Hemmkonzentration dieser neuen Verbindungsklasse ist aus den nachfolgenden Tabellen ersichtlich.; ' carry from 6 to 8 carbon atoms, being too it must be taken into account that the optimal effectiveness largely depends on the requirements set, e.g. solubility, stability, etc. Part of the compounds is due to its solubility and bactericidal activity in a number of organic solvents of particular interest. The minimum inhibitory concentration of this new class of compounds is from the tables below evident.
609 709/297609 709/297
3 43 4
Tabelle 1.
Minimale Hemmkonzentration derAusgangsprodukte, Angaben in y/mlTable 1.
Minimum inhibitory concentration of the starting products, data in y / ml
Verbindunglink
Staph. aureusStaph. aureus
Escherich, coliEscherich, coli
Pseudom.
aerugin.Pseudom.
aerugin.
Proteus
vulgarisProteus
vulgaris
Asperg, nigerAsperg, niger
TrialkylphosphiteTrialkyl phosphites
Triäthyl- ......... Triethyl .........
Tributyl· \ί:\...... / Tributyl \ ί: \. ..... /
Trioctyl- Trioctyl
Tridodecyl- Tridodecyl
TrialkylphosphateTrialkyl phosphates
Triäthyl- ...:.:........ Triethyl- ...:.: ........
Tributyl- Tributyl
Trihexyl- Trihexyl
Trioctyl- Trioctyl
Tridodecyl- Tridodecyl
Mischungen aus Mono- und Dialkylphosphorsäuren (gleiche Alkylreste, Verhältnis 1:1)Mixtures of mono- and dialkyl phosphoric acids (same alkyl radicals, ratio 1: 1)
Methyl- viivi;,....:.. Methyl viivi;, ....: ..
.Äthyl·' ^iai^. .Ethyl · ' ^ iai ^.
Butyl- Butyl
Hexyl- Hexyl
Octyl- Octyl
Dodecyl- Dodecyl
800 800 800 800 800800 800 800 800 800
800 400 800 800 800800 400 800 800 800
400400
100100
100100
5050
5050
100100
400 400 200 100 100 100400 400 200 100 100 100
800
800
800
800
800800
800
800
800
800
800
800
800
800
800800
800
800
800
800
200200
100100
100100
100100
5050
5050
800
800
800
800
800800
800
800
800
800
■■gor■■ gor
800
800
800
800800
800
800
800
400400
400400
400400
100100
5050
5050
800 800 800 800 800800 800 800 800 800
800'800 '
800800
800800
800800
800800
800 800 800 400 400 >400800 800 800 400 400> 400
Minimale Hemmkonzentration der Kondensationsprodukte der in Tabelle 1 aufgeführten Ausgangsverbindungen mit 20 bis 25°/o Phosphorpentoxyd, Angaben in y/mlMinimum inhibitory concentration of the condensation products of the starting compounds listed in Table 1 with 20 to 25% phosphorus pentoxide, data in y / ml
sperg. Desulfovi-sperg. Desulfovi-
liger brioliger brio
Phosphorpentoxydkondensations-Phosphorus pentoxide condensation
produkt mitproduct with
Triäthylphosphit ..:. 25 25 50 50 400 10Triethyl phosphite ..:. 25 25 50 50 400 10
Tributylphosphit 25 25 50 25 250 5Tributyl phosphite 25 25 50 25 250 5
Trihexylphosphit 6 12 12 12 125 1Trihexyl phosphite 6 12 12 12 125 1
Isooctylphosphit ..', 0,5 1 0,5 0,5 62,5 0,5Isooctyl phosphite .. ', 0.5 1 0.5 0.5 62.5 0.5
TrioctylphospMt 3 12 12 12 125 3TrioctylphosphMt 3 12 12 12 125 3
Triäthylhexylphosphit 0,5 1 0,5 0,5 · 62,5 0,5Triethylhexyl phosphite 0.5 1 0.5 0.5 x 62.5 0.5
Tridodecylphosphit 6 25 25 50 400 10Tridodecyl phosphite 6 25 25 50 400 10
Triäthylphosphat: 3 25 25 25 250 5Triethyl phosphate: 3 25 25 25 250 5
Tributylphosphat 3 25 50 50 400 10Tributyl phosphate 3 25 50 50 400 10
Trihexylphosphat 3 12 12 25 250 5Trihexyl phosphate 3 12 12 25 250 5
Trioctylphosphat 1 12 12 12 250 5Trioctyl phosphate 1 12 12 12 250 5
Tridodecylphosphat 6 50 50 50 400 50Tridodecyl phosphate 6 50 50 50 400 50
Diäthyläther 3 25 25 25 250 5Diethyl ether 3 25 25 25 250 5
Phosphorpentoxydkondensations-Phosphorus pentoxide condensation
produkt mit Gemischen aus Mono-product with mixtures of mono-
und Dialkylphosphorsäuren (gleicheand dialkyl phosphoric acids (same
Alfcylreste, Verhältnis 1:1) auf BasisAlfcyl residues, ratio 1: 1) based on
Methyl- 12 25 50 50 400 25Methyl 12 25 50 50 400 25
Äthyl- :..... 3 12 25 25 250 12Ethyl: ..... 3 12 25 25 250 12
Butyl- 3 12 25 25 250 12Butyl 3 12 25 25 250 12
Hexyl- '. 1 12 12 12 125 6Hexyl- '. 1 12 12 12 125 6
Octyl- '.:. 1 6 12 12 125 6Octyl- '.:. 1 6 12 12 125 6
Dodecyl- ....'. 6 25 25 25 400 25Dodecyl- .... '. 6 25 25 25 400 25
Claims (4)
vorzugsweise 30 %> Phosphorpentoxyd erhalten 3. Use according to claims 1 and 2, in the proportion of to be used according to the invention, characterized in that the condensation to the polyphosphoric acid derivatives should be at least 25% »products by reaction with up to about 35%» 5, preferably 50% »,
preferably 30%> phosphorus pentoxide obtained
durch gekennzeichnet, daß die Kondensations- USA.-Patentschrift Nr. 2402703.4. Use according to Claims 1 to 3, since the documents considered:
characterized in that Condensation U.S. Patent No. 2402703.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF46300A DE1228031B (en) | 1965-06-11 | 1965-06-11 | Bactericidal |
LU51194D LU51194A1 (en) | 1965-06-11 | 1966-05-26 | |
NL6607823A NL6607823A (en) | 1965-06-11 | 1966-06-06 | |
FR1490608D FR1490608A (en) | 1965-06-11 | 1966-06-10 | New bactericides |
SE794166A SE319579B (en) | 1965-06-11 | 1966-06-10 | |
DK301466A DK113515B (en) | 1965-06-11 | 1966-06-10 | Disinfectant or preservative. |
BE682445D BE682445A (en) | 1965-06-11 | 1966-06-13 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF46300A DE1228031B (en) | 1965-06-11 | 1965-06-11 | Bactericidal |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1228031B true DE1228031B (en) | 1966-11-03 |
Family
ID=7100956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF46300A Pending DE1228031B (en) | 1965-06-11 | 1965-06-11 | Bactericidal |
Country Status (7)
Country | Link |
---|---|
BE (1) | BE682445A (en) |
DE (1) | DE1228031B (en) |
DK (1) | DK113515B (en) |
FR (1) | FR1490608A (en) |
LU (1) | LU51194A1 (en) |
NL (1) | NL6607823A (en) |
SE (1) | SE319579B (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0197128A1 (en) * | 1984-10-09 | 1986-10-15 | Interface Res Corp | Microbiocidal composition and method of preparation thereof. |
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/en active Pending
-
1966
- 1966-05-26 LU LU51194D patent/LU51194A1/xx unknown
- 1966-06-06 NL NL6607823A patent/NL6607823A/xx unknown
- 1966-06-10 FR FR1490608D patent/FR1490608A/en not_active Expired
- 1966-06-10 SE SE794166A patent/SE319579B/xx unknown
- 1966-06-10 DK DK301466A patent/DK113515B/en unknown
- 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 | Microbiocidal composition and method of preparation thereof. |
EP0197128A4 (en) * | 1984-10-09 | 1989-07-25 | Interface Res Corp | Microbiocidal composition and method of preparation thereof. |
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 |
---|---|
SE319579B (en) | 1970-01-19 |
FR1490608A (en) | 1967-08-04 |
LU51194A1 (en) | 1968-02-21 |
NL6607823A (en) | 1966-12-12 |
DK113515B (en) | 1969-03-31 |
BE682445A (en) | 1966-12-13 |
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