CN1093850C - 邻苯二醛－戊二醛水溶液的制备方法 - Google Patents
邻苯二醛－戊二醛水溶液的制备方法 Download PDFInfo
- Publication number
- CN1093850C CN1093850C CN97126296A CN97126296A CN1093850C CN 1093850 C CN1093850 C CN 1093850C CN 97126296 A CN97126296 A CN 97126296A CN 97126296 A CN97126296 A CN 97126296A CN 1093850 C CN1093850 C CN 1093850C
- Authority
- CN
- China
- Prior art keywords
- solution
- glutaraldehyde
- opa
- acetal
- alcohol
- 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.)
- Expired - Fee Related
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- ZWLUXSQADUDCSB-UHFFFAOYSA-N phthalaldehyde Chemical compound O=CC1=CC=CC=C1C=O ZWLUXSQADUDCSB-UHFFFAOYSA-N 0.000 claims abstract description 38
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 19
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims abstract description 15
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 15
- BHTJEPVNHUUIPV-UHFFFAOYSA-N pentanedial;hydrate Chemical compound O.O=CCCCC=O BHTJEPVNHUUIPV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 238000004821 distillation Methods 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 230000008030 elimination Effects 0.000 claims description 3
- 238000003379 elimination reaction Methods 0.000 claims description 3
- 229940054441 o-phthalaldehyde Drugs 0.000 abstract 2
- 239000000243 solution Substances 0.000 description 45
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 17
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 150000001335 aliphatic alkanes Chemical class 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 4
- SZKKRCSOSQAJDE-UHFFFAOYSA-N Schradan Chemical compound CN(C)P(=O)(N(C)C)OP(=O)(N(C)C)N(C)C SZKKRCSOSQAJDE-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- -1 OPA acetal Chemical class 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 239000003637 basic solution Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 101100232929 Caenorhabditis elegans pat-4 gene Proteins 0.000 description 1
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RHDGNLCLDBVESU-UHFFFAOYSA-N but-3-en-4-olide Chemical compound O=C1CC=CO1 RHDGNLCLDBVESU-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003822 preparative gas chromatography Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aldehyde or keto groups, or thio analogues thereof, directly attached to an aromatic ring system, e.g. acetophenone; Derivatives thereof, e.g. acetals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Health & Medical Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT0205396A AT404592B (de) | 1996-11-26 | 1996-11-26 | Verfahren zur herstellung von wässrigen o-phthalaldehyd-glutaraldehydlösungen |
| AT2053A/96 | 1996-11-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1185428A CN1185428A (zh) | 1998-06-24 |
| CN1093850C true CN1093850C (zh) | 2002-11-06 |
Family
ID=3526769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN97126296A Expired - Fee Related CN1093850C (zh) | 1996-11-26 | 1997-11-25 | 邻苯二醛－戊二醛水溶液的制备方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5872153A (cg-RX-API-DMAC7.html) |
| EP (1) | EP0843966B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP3968160B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1093850C (cg-RX-API-DMAC7.html) |
| AT (2) | AT404592B (cg-RX-API-DMAC7.html) |
| DE (1) | DE59708182D1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK0843966T3 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2180877T3 (cg-RX-API-DMAC7.html) |
| IN (1) | IN187090B (cg-RX-API-DMAC7.html) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040071592A1 (en) * | 2002-10-10 | 2004-04-15 | Ioana Annis | Fast dissolving solid ortho-phthalic aldehyde formulations |
| AT501448B1 (de) * | 2005-03-02 | 2006-11-15 | Dsm Fine Chem Austria Gmbh | Verfahren zur herstellung von wässrigen ortho-phthalaldehyd-lösungen |
| US7291649B2 (en) * | 2005-06-29 | 2007-11-06 | Ethicon, Inc. | Forming germicidal aromatic dialdehydes with acetals |
| CA2797061C (en) | 2010-04-27 | 2016-02-09 | Whiteley Corporation Pty Ltd | Synergistic, non-equilibrium aldehyde biocides |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5128051A (en) * | 1991-09-30 | 1992-07-07 | Union Carbide Chemicals & Plastics Technology Corporation | Method for the control of biofouling |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4244876A (en) * | 1978-11-17 | 1981-01-13 | Union Carbide Corporation | Acetal-acid compositions |
| DE3108790A1 (de) * | 1981-03-07 | 1982-09-16 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur herstellung von bis(dialkoximethyl)benzolen |
| US4847304A (en) * | 1987-05-21 | 1989-07-11 | Surgikos, Inc. | Disinfecting and sterilizing composition |
| DE4122314A1 (de) * | 1991-07-05 | 1993-01-07 | Basf Ag | O-phthaldialdehydtetraalkylacetale, ihre herstellung und ihre verwendung als depotverbindung |
| DE4407986A1 (de) * | 1993-03-19 | 1994-09-22 | Basf Ag | Verfahren zur Herstellung von o-Phthalaldehydtetraalkylacetalen |
| US5723498A (en) * | 1994-11-21 | 1998-03-03 | Degussa Aktiengellschaft | Composition capable of releasing acrolein and its use |
-
1996
- 1996-11-26 AT AT0205396A patent/AT404592B/de not_active IP Right Cessation
-
1997
- 1997-11-17 IN IN3284DE1997 patent/IN187090B/en unknown
- 1997-11-18 DE DE59708182T patent/DE59708182D1/de not_active Expired - Fee Related
- 1997-11-18 AT AT97120163T patent/ATE223647T1/de not_active IP Right Cessation
- 1997-11-18 EP EP97120163A patent/EP0843966B1/de not_active Expired - Lifetime
- 1997-11-18 ES ES97120163T patent/ES2180877T3/es not_active Expired - Lifetime
- 1997-11-18 DK DK97120163T patent/DK0843966T3/da active
- 1997-11-25 JP JP32316997A patent/JP3968160B2/ja not_active Expired - Fee Related
- 1997-11-25 CN CN97126296A patent/CN1093850C/zh not_active Expired - Fee Related
- 1997-11-26 US US08/979,952 patent/US5872153A/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5128051A (en) * | 1991-09-30 | 1992-07-07 | Union Carbide Chemicals & Plastics Technology Corporation | Method for the control of biofouling |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1185428A (zh) | 1998-06-24 |
| IN187090B (cg-RX-API-DMAC7.html) | 2002-01-26 |
| EP0843966B1 (de) | 2002-09-11 |
| AT404592B (de) | 1998-12-28 |
| DE59708182D1 (de) | 2002-10-17 |
| JPH10182539A (ja) | 1998-07-07 |
| US5872153A (en) | 1999-02-16 |
| JP3968160B2 (ja) | 2007-08-29 |
| ATE223647T1 (de) | 2002-09-15 |
| EP0843966A1 (de) | 1998-05-27 |
| ATA205396A (de) | 1998-05-15 |
| DK0843966T3 (da) | 2002-10-07 |
| ES2180877T3 (es) | 2003-02-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Marshall | Structure studies on vancomycin | |
| US5606107A (en) | Formic acid and formaldehyde destruction in waste streams | |
| CN1185428A (zh) | 邻苯二醛－戊二醛水溶液的制备方法 | |
| JPH0672116B2 (ja) | グリオキサール−又はアルキルグリオキサール−アセタールの製造方法 | |
| US4244876A (en) | Acetal-acid compositions | |
| CN1116268C (zh) | 纯化邻苯二醛的方法 | |
| DE69606384T2 (de) | Verfahren zur Herstellung von N-monosubstituierten Hydroxylaminen | |
| DE69303360T2 (de) | Oxydation von Glykolsäure zur Herstellung von Glyoxylsäure unter Verwendung von transformierten mikrobiellen Zellen als Katalysator. | |
| DE102005029094A1 (de) | Verfahren zur Herstellung von Pyridazin | |
| EP0645368B1 (de) | Verfahren zur Reinigung tertiärer Amine von primären und sekundären Aminen | |
| US4542235A (en) | Method for producing an optically active 2,2-dimethylcyclopropanecarboxylic acid | |
| CN115552672B (zh) | 在氧化还原液流电池中用作电解质的tempo衍生物的溶液 | |
| CA1298857C (fr) | Procede pour la fabrication de l'acide beta- hydroxybutyrique etde ses sels par hydrolyse d'oligomeres de l'acide beta-hydroxybutyrique en milieu basique | |
| US5502188A (en) | Production of almost colorless solutions of n-methylmorpholine oxide | |
| DE69528160T2 (de) | Verfahren zur herstellung von 5,7 dichlor-4-hydroxychinolin | |
| EP0059655A1 (fr) | Procédé d'obtention de l'epsilon-caprolactone | |
| CN1242974C (zh) | 制备一氯乙酸的方法 | |
| US5770767A (en) | Process for producing 2-fluorocyclopropancecarboxlic acid | |
| US20070100167A1 (en) | Process for synthesizing heliotropine and its derivatives | |
| WO2006034692A1 (de) | VERFAHREN ZUR HYDRIERUNG VON α,β-UNGESÄTTIGTEN CARBONYLVERBINDUNGEN | |
| EP0065356B1 (en) | A method for purification of cyclopentenolones | |
| EP0029092B1 (en) | Cis-(1r,2s)-3,3-dimethyl-2-((4s)-3-methyl-2-(2-propynyl)cyclopent-2-en-1-on-4-yloxyhydroxymethyl)-cyclopropanecarboxylic lactone and method of producing (s)-4-hydroxy-3-methyl-2-(2-propynyl)-cyclopent-2-en-1-on | |
| CN1845899A (zh) | 高纯度3,5－二羟基－6－庚烯酸衍生物的制备方法 | |
| EP0170937B1 (fr) | Sulfate double de desoxyfructosyl-sérotonine et de créatinine, sa préparation et médicament le contenant | |
| US6844467B2 (en) | Method for the production of glyceric acid |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |