DE1249457B - Verwendung von Alkyl dl guamdmsalzen als Mii-robizide - Google Patents
Verwendung von Alkyl dl guamdmsalzen als Mii-robizideInfo
- Publication number
- DE1249457B DE1249457B DENDAT1249457D DE1249457DA DE1249457B DE 1249457 B DE1249457 B DE 1249457B DE NDAT1249457 D DENDAT1249457 D DE NDAT1249457D DE 1249457D A DE1249457D A DE 1249457DA DE 1249457 B DE1249457 B DE 1249457B
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- cyanamide
- mixture
- water
- acetic acid
- 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
- 125000000217 alkyl group Chemical group 0.000 title claims description 9
- 150000003839 salts Chemical class 0.000 title description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 230000003641 microbiacidal effect Effects 0.000 claims description 6
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229940124561 microbicide Drugs 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 238000005108 dry cleaning Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 229960000583 acetic acid Drugs 0.000 claims 2
- 235000013162 Cocos nucifera Nutrition 0.000 claims 1
- 244000060011 Cocos nucifera Species 0.000 claims 1
- 241000588724 Escherichia coli Species 0.000 claims 1
- 102000002265 Human Growth Hormone Human genes 0.000 claims 1
- 108010000521 Human Growth Hormone Proteins 0.000 claims 1
- 239000000854 Human Growth Hormone Substances 0.000 claims 1
- 241000588767 Proteus vulgaris Species 0.000 claims 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 claims 1
- 241000194017 Streptococcus Species 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 229940023064 escherichia coli Drugs 0.000 claims 1
- 239000012362 glacial acetic acid Substances 0.000 claims 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims 1
- 239000003208 petroleum Substances 0.000 claims 1
- 229940007042 proteus vulgaris Drugs 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 229940063153 saizen Drugs 0.000 claims 1
- 238000001228 spectrum Methods 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 239000000052 vinegar Substances 0.000 claims 1
- 235000021419 vinegar Nutrition 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 7
- 150000002357 guanidines Chemical class 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 208000031531 Desulfovibrionaceae Infections Diseases 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- -1 alkyl diamine salts Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 150000004023 quaternary phosphonium compounds Chemical class 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/605—Compositions for stimulating production by acting on the underground formation containing biocides
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0047056 | 1965-09-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1249457B true DE1249457B (de) | 1967-09-07 |
Family
ID=7101393
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT1249457D Pending DE1249457B (de) | 1965-09-01 | Verwendung von Alkyl dl guamdmsalzen als Mii-robizide |
Country Status (4)
| Country | Link |
|---|---|
| AT (2) | AT271495B (enExample) |
| DE (1) | DE1249457B (enExample) |
| GB (1) | GB1156517A (enExample) |
| NL (1) | NL6612197A (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2952167A1 (de) * | 1979-12-22 | 1981-07-02 | Hoechst Ag, 6230 Frankfurt | Neue guanidiniumverbindungen, verfahren zu deren herstellung und deren verwendung als mikrobiozide mittel |
| DE3531356A1 (de) * | 1985-09-03 | 1987-03-12 | Hoechst Ag | Mikrobiozide mittel auf basis von alkyl-di-guanidiniumsalzen |
| CN108689888B (zh) * | 2018-05-16 | 2021-06-04 | 中国日用化学研究院有限公司 | 一种烷基二胍盐及其制备方法 |
| CN109704997A (zh) * | 2019-01-21 | 2019-05-03 | 华南农业大学 | 含胍基类化合物的消毒剂及其制备方法 |
-
0
- DE DENDAT1249457D patent/DE1249457B/de active Pending
-
1966
- 1966-08-30 AT AT504068A patent/AT271495B/de active
- 1966-08-30 NL NL6612197A patent/NL6612197A/xx unknown
- 1966-08-30 AT AT822066A patent/AT271494B/de active
- 1966-09-01 GB GB3912866A patent/GB1156517A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AT271494B (de) | 1969-06-10 |
| NL6612197A (enExample) | 1967-03-02 |
| GB1156517A (en) | 1969-06-25 |
| AT271495B (de) | 1969-06-10 |
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