ATA227880A - METHOD FOR PRODUCING NEW CHLORHEXIDINE SALTS - Google Patents

METHOD FOR PRODUCING NEW CHLORHEXIDINE SALTS

Info

Publication number
ATA227880A
ATA227880A AT0227880A AT227880A ATA227880A AT A227880 A ATA227880 A AT A227880A AT 0227880 A AT0227880 A AT 0227880A AT 227880 A AT227880 A AT 227880A AT A227880 A ATA227880 A AT A227880A
Authority
AT
Austria
Prior art keywords
producing new
chlorhexidine salts
new chlorhexidine
salts
producing
Prior art date
Application number
AT0227880A
Other languages
German (de)
Other versions
AT373235B (en
Original Assignee
Bristol Myers Co
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.)
Filing date
Publication date
Application filed by Bristol Myers Co filed Critical Bristol Myers Co
Priority to AT149983A priority Critical patent/AT386951B/en
Publication of ATA227880A publication Critical patent/ATA227880A/en
Application granted granted Critical
Publication of AT373235B publication Critical patent/AT373235B/en
Priority to AT163086A priority patent/AT386952B/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C279/20—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
    • C07C279/24—Y being a hetero atom
    • C07C279/26—X and Y being nitrogen atoms, i.e. biguanides
    • C07C279/265—X and Y being nitrogen atoms, i.e. biguanides containing two or more biguanide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/03—Monocarboxylic acids
    • C07C57/10—Sorbic acid
    • 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 System
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
    • C07F9/3804—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se) not used, see subgroups
    • C07F9/3834—Aromatic acids (P-C aromatic linkage)
AT0227880A 1979-04-26 1980-04-28 METHOD FOR PRODUCING NEW CHLORHEXIDINE SALTS AT373235B (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AT149983A AT386951B (en) 1979-04-26 1983-04-25 Process for the production of antibacterial mixtures
AT163086A AT386952B (en) 1979-04-26 1986-06-16 Process for the production of antibacterial mixtures

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3359379A 1979-04-26 1979-04-26

Publications (2)

Publication Number Publication Date
ATA227880A true ATA227880A (en) 1983-05-15
AT373235B AT373235B (en) 1983-12-27

Family

ID=21871298

Family Applications (1)

Application Number Title Priority Date Filing Date
AT0227880A AT373235B (en) 1979-04-26 1980-04-28 METHOD FOR PRODUCING NEW CHLORHEXIDINE SALTS

Country Status (13)

Country Link
JP (1) JPS55149242A (en)
AT (1) AT373235B (en)
CA (1) CA1159834A (en)
CH (2) CH646948A5 (en)
CY (2) CY1324A (en)
DE (1) DE3016110A1 (en)
ES (1) ES490947A0 (en)
FR (1) FR2455034A1 (en)
GB (2) GB2053195B (en)
HK (2) HK1486A (en)
IT (1) IT1188929B (en)
MY (2) MY8600498A (en)
NL (1) NL8002483A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050058673A1 (en) * 2003-09-09 2005-03-17 3M Innovative Properties Company Antimicrobial compositions and methods
BRPI0608691A2 (en) 2005-03-10 2010-12-07 3M Innovative Properties Co antimicrobial composition, and methods for killing or inactivating microorganisms in mammalian mucosal tissue, for treating an infected injury or wound, for decolonizing microorganisms, for providing residual antimicrobial efficacy on a surface, and for treating a condition
WO2006099325A2 (en) 2005-03-10 2006-09-21 3M Innovative Properties Company Methods of treating ear infections
AU2006223137A1 (en) 2005-03-10 2006-09-21 3M Innovative Properties Company Methods of reducing microbial contamination
US20130065965A1 (en) * 2009-11-18 2013-03-14 Medichem S.A. Di(4-chloro-phenyldiguanido) derivative which is free of potential genotoxicity and a process for reducing the residual amount of p-chloroaniline in said di(4-chloro-phenyldiguanido) derivative

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB815800A (en) * 1956-06-06 1959-07-01 Ici Ltd New biguanide salts
US2684924A (en) * 1951-02-05 1954-07-27 Ici Ltd Nu-chlorophenyldiguanidino compounds
US2990425A (en) * 1956-06-06 1961-06-27 Ici Ltd New biguanide salts
US3159537A (en) * 1960-12-20 1964-12-01 American Cyanamid Co Potentiation of tetracycline by phosphinic acid
BE612641A (en) * 1961-01-18
US3694447A (en) * 1970-03-10 1972-09-26 Smith Kline French Lab Complexes of phosphanilic acid and 9-amino-3-nitroacridine
US3794723A (en) * 1970-03-10 1974-02-26 Smithkline Corp Complexes of phosphanilic acid and 9-amino-3-nitroacridine useful as antifungal or antibacterial agents
SE370003B (en) * 1971-05-18 1974-09-30 Kema Nord Ab
GB1338003A (en) * 1971-06-18 1973-11-21 Ici Ltd Cleaning compositions
SE374658B (en) * 1972-07-31 1975-03-17 Hesselgren S G
US3976765A (en) * 1973-11-01 1976-08-24 Colgate-Palmolive Company Antibacterial oral preparations
US4125610A (en) * 1977-07-27 1978-11-14 Bristol-Myers Company Antibacterial compositions

Also Published As

Publication number Publication date
GB2118041B (en) 1984-03-21
IT8048512A0 (en) 1980-04-24
CH646948A5 (en) 1984-12-28
FR2455034A1 (en) 1980-11-21
AT373235B (en) 1983-12-27
CA1159834A (en) 1984-01-03
CY1324A (en) 1986-06-27
HK1486A (en) 1986-01-17
MY8600498A (en) 1986-12-31
GB2053195A (en) 1981-02-04
CH648755A5 (en) 1985-04-15
GB2053195B (en) 1983-04-07
IT8048512A1 (en) 1981-10-24
FR2455034B1 (en) 1984-08-10
DE3016110A1 (en) 1980-11-06
DE3016110C2 (en) 1990-12-13
HK21286A (en) 1986-04-04
GB2118041A (en) 1983-10-26
IT1188929B (en) 1988-01-28
NL8002483A (en) 1980-10-28
ES8105259A1 (en) 1981-05-16
ES490947A0 (en) 1981-05-16
CY1316A (en) 1986-03-28
JPS55149242A (en) 1980-11-20
MY8600495A (en) 1986-12-31

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Legal Events

Date Code Title Description
ELJ Ceased due to non-payment of the annual fee