DE157553C - - Google Patents
Info
- Publication number
- DE157553C DE157553C DE1903157553D DE157553DA DE157553C DE 157553 C DE157553 C DE 157553C DE 1903157553 D DE1903157553 D DE 1903157553D DE 157553D A DE157553D A DE 157553DA DE 157553 C DE157553 C DE 157553C
- Authority
- DE
- Germany
- Prior art keywords
- formaldehyde
- water
- phenol
- product
- reaction
- 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 - Lifetime
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 41
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 17
- 239000000047 product Substances 0.000 claims description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000007859 condensation product Substances 0.000 claims description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
- 239000002253 acid Substances 0.000 claims 2
- 239000008098 formaldehyde solution Substances 0.000 claims 2
- 235000011121 sodium hydroxide Nutrition 0.000 claims 2
- DIZBQMTZXOUFTD-UHFFFAOYSA-N 2-(furan-2-yl)-3h-benzimidazole-5-carboxylic acid Chemical compound N1C2=CC(C(=O)O)=CC=C2N=C1C1=CC=CO1 DIZBQMTZXOUFTD-UHFFFAOYSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 238000000354 decomposition reaction Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 238000012552 review Methods 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 6
- 239000012670 alkaline solution Substances 0.000 description 4
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 3
- 235000006173 Larrea tridentata Nutrition 0.000 description 3
- 244000073231 Larrea tridentata Species 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229960002126 creosote Drugs 0.000 description 3
- 229960001867 guaiacol Drugs 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002141 anti-parasite Effects 0.000 description 1
- 230000000721 bacterilogical effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000012678 infectious agent Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- -1 phenol formaldehyde compound Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT25223D AT25223B (de) | 1903-02-21 | 1905-02-08 | Verfahren zur Darstellung eines Kondensationsproduktes aus Phenol und Formaldehyd. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE157553C true DE157553C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=423811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1903157553D Expired - Lifetime DE157553C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1903-02-21 | 1903-02-21 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE157553C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1003956B (de) * | 1954-06-08 | 1957-03-07 | Leuna Werke Iawalter Ulbrichti | Verfahren zur Herstellung von wasserhaltigen, fluessigen Kunstharzen aus Phenolen und Aldehyden |
-
1903
- 1903-02-21 DE DE1903157553D patent/DE157553C/de not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1003956B (de) * | 1954-06-08 | 1957-03-07 | Leuna Werke Iawalter Ulbrichti | Verfahren zur Herstellung von wasserhaltigen, fluessigen Kunstharzen aus Phenolen und Aldehyden |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE157553C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE102007003693A1 (de) | Desinfektionsmittel | |
| DE902170C (de) | Verfahren zum Entgiften von halogenhaltigen pharmazeutischen Produkten | |
| AT48607B (de) | Verfahren zur Herstellung jodhaltiger Produkte aus Aldehyden und Ketonen. | |
| DE519531C (de) | Verfahren zur Herstellung einer leicht wasserloeslichen, kolloidalen Silber-Tannin-Eiweissverbindung | |
| AT18981B (de) | Verfahren zur Herstellung eines Teer-Formaldehydpräparates. | |
| AT25223B (de) | Verfahren zur Darstellung eines Kondensationsproduktes aus Phenol und Formaldehyd. | |
| DE633786C (de) | Verfahren zur Herstellung von Komplexverbindungen des 1, 3-Dimethylxanthins | |
| AT48581B (de) | Verfahren zur Darstellung von zu internen Desinfektionszwecken geeigneten Phenol-Eiweißverbindungen. | |
| DE363302C (de) | Verfahren zur Herstellung von Desinfektionsmitteln | |
| DE495336C (de) | Verfahren zur Darstellung von basischen Oximaethern und ihren Salzen | |
| DE704549C (de) | Verfahren zur Herstellung von Pplyjodoxyphenylphenylessigsaeuren | |
| DE141744C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE483357C (de) | Verfahren zur Herstellung von alkoholhaltigen teigigen bis festen Massen | |
| DE194810C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE237089C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| AT96660B (de) | Verfahren zur Herstellung schellackartiger Kondensationsprodukte aus Phenolen und polymerisiertem Formaldehyd. | |
| DE227177C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| AT112135B (de) | Verfahren zur Darstellung von basischen Oximäthern und ihren Salzen. | |
| DE188318C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| AT153203B (de) | Verfahren zur Darstellung wasserlöslicher Quecksilberverbindungen. | |
| DE886743C (de) | Verfahren zur Herstellung von Aminomercaptalen | |
| CH616448A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| AT142713B (de) | Verfahren zur Herstellung von in Lösungen haltbaren Präparaten, die anaesthesierend wirkende und gefäßverengende Mittel enthalten. | |
| DE49739C (de) | Verfahren zur Darstellung von Jodverbindungen des Thymols und ;J-Naphtols |