DE212070C - - Google Patents
Info
- Publication number
- DE212070C DE212070C DENDAT212070D DE212070DA DE212070C DE 212070 C DE212070 C DE 212070C DE NDAT212070 D DENDAT212070 D DE NDAT212070D DE 212070D A DE212070D A DE 212070DA DE 212070 C DE212070 C DE 212070C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- salts
- formaldehyde
- acetaldehyde
- parts
- 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.)
- Active
Links
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical class CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- -1 disulfoacetaldehyde sulfoxylic acid Chemical class 0.000 claims description 4
- 239000003638 chemical reducing agent Substances 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- AHFCTDMSWZTREU-UHFFFAOYSA-N acetaldehyde;sulfanediol Chemical class CC=O.OSO AHFCTDMSWZTREU-UHFFFAOYSA-N 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- QJQZEJFUIOWFMS-UHFFFAOYSA-N formaldehyde;sulfanediol Chemical class O=C.OSO QJQZEJFUIOWFMS-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- UBZYWIKLAYTIOV-UHFFFAOYSA-N [Na].CC=O Chemical compound [Na].CC=O UBZYWIKLAYTIOV-UHFFFAOYSA-N 0.000 description 1
- 238000010018 discharge printing Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE212070C true DE212070C (Sortimente) |
Family
ID=473825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT212070D Active DE212070C (Sortimente) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE212070C (Sortimente) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2671800A (en) * | 1948-11-16 | 1954-03-09 | Gen Aniline & Film Corp | Process of preparing bisulfite addition products of malonaldehyde |
-
0
- DE DENDAT212070D patent/DE212070C/de active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2671800A (en) * | 1948-11-16 | 1954-03-09 | Gen Aniline & Film Corp | Process of preparing bisulfite addition products of malonaldehyde |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE212070C (Sortimente) | ||
| DE2850948A1 (de) | Pyridinderivat, verfahren zu seiner herstellung und arzneimittel | |
| CN1120158C (zh) | 甲酰基咪唑的制备方法 | |
| DE208790C (Sortimente) | ||
| DE475937C (de) | Verfahren zur Darstellung organischer Arsenoverbindungen | |
| DE2123621C3 (de) | Verfahren zur Herstellung von Aldonsäuren | |
| DE260235C (Sortimente) | ||
| DE102005030882A1 (de) | Katalysator und Verfahren zur Herstellung von Carboxylsäure-Estern | |
| DE164664C (Sortimente) | ||
| DE922166C (de) | Verfahren zur Umwandlung olefinischer Aldehyde in Oxyaldehyde | |
| DE2634783C2 (de) | Verfahren zur Herstellung von Schwefelsäurehalbester-Verbindungen | |
| DE887945C (de) | Verfahren zur Herstellung von reinstem Aluminiumacetat mit niedrigem Essigsaeuregehalt | |
| DE917005C (de) | Verfahren zur Herstellung quecksilberhaltiger Propylharnstoffe | |
| DE415320C (de) | Verfahren zur Herstellung von 2-Oxy-1-arylaminonaphthalinsulfosaeuren | |
| EP0059259B1 (de) | Verfahren zur Herstellung von N-(Carboxy-alkyl)-1-amino-alkan-1,1-diphosphonsäuren und deren Alkalisalze | |
| DE635297C (de) | Verfahren zur Herstellung von wasserloeslichen, sauren, esterartigen Kondensationsprodukten | |
| EP1174435A2 (de) | Verfahren zur Herstellung von Platin-Alkenylpolysiloxan-Komplexen, insbesondere von Platin-Divinyltetramethyldisiloxan | |
| DE202826C (Sortimente) | ||
| DE635398C (de) | Verfahren zur Darstellung von Arsenobenzomonosulfoxylaten | |
| DE2225367C3 (de) | Verfahren zur Herstellung von Diglykolsäure | |
| DE749149C (de) | Verfahren zur Herstellung eines Aneurin-Oxydationsproduktes | |
| DE825407C (de) | Verfahren zur Herstellung von loeslichen Goldverbindungen | |
| DE937948C (de) | Verfahren zur Herstellung von Salzen der 3-Oxypropan-1-sulfonsaeure | |
| DE2024062C3 (de) | Verfahren zur Abtrennung und Ge winnung von L Lysin | |
| DE666573C (de) | Verfahren zur Herstellung von aminosubstituierten Arsenobenzolformaldehydbisulfit-verbindungen |