DE114396C - - Google Patents
Info
- Publication number
- DE114396C DE114396C DE1899114396D DE114396DA DE114396C DE 114396 C DE114396 C DE 114396C DE 1899114396 D DE1899114396 D DE 1899114396D DE 114396D A DE114396D A DE 114396DA DE 114396 C DE114396 C DE 114396C
- Authority
- DE
- Germany
- Prior art keywords
- urethane
- urethanes
- sleep
- urea
- secondary alcohols
- 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
- 230000000694 effects Effects 0.000 claims description 7
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 claims description 6
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 claims description 6
- 150000003333 secondary alcohols Chemical class 0.000 claims description 5
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-methyl-2-butanol Chemical compound CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- ISTJMQSHILQAEC-UHFFFAOYSA-N 2-methyl-3-pentanol Chemical compound CCC(O)C(C)C ISTJMQSHILQAEC-UHFFFAOYSA-N 0.000 claims description 3
- YVBCULSIZWMTFY-UHFFFAOYSA-N Heptan-4-ol Chemical compound CCCC(O)CCC YVBCULSIZWMTFY-UHFFFAOYSA-N 0.000 claims description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 3
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- ZOCHHNOQQHDWHG-UHFFFAOYSA-N hexan-3-ol Chemical compound CCCC(O)CC ZOCHHNOQQHDWHG-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 11
- 150000003673 urethanes Chemical class 0.000 description 8
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 241000282472 Canis lupus familiaris Species 0.000 description 3
- 230000000147 hypnotic effect Effects 0.000 description 3
- QHDUJTCUPWHNPK-UHFFFAOYSA-N methyl 7-methoxy-2h-indazole-3-carboxylate Chemical compound COC1=CC=CC2=C(C(=O)OC)NN=C21 QHDUJTCUPWHNPK-UHFFFAOYSA-N 0.000 description 3
- 206010002091 Anaesthesia Diseases 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- 230000037005 anaesthesia Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- -1 methylethylcarbinol urethane Chemical compound 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000269350 Anura Species 0.000 description 1
- 241001440205 Phyllomedusinae Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 1
- 229960002327 chloral hydrate Drugs 0.000 description 1
- 239000003326 hypnotic agent Substances 0.000 description 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
- LKACJLUUJRMGFK-UHFFFAOYSA-N methylsulfonal Chemical compound CCS(=O)(=O)C(C)(CC)S(=O)(=O)CC LKACJLUUJRMGFK-UHFFFAOYSA-N 0.000 description 1
- 229950006999 methylsulfonal Drugs 0.000 description 1
- 230000003533 narcotic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT4545D AT4545B (it) | 1899-04-01 | 1900-09-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE114396C true DE114396C (it) |
Family
ID=383901
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1899114396D Expired - Lifetime DE114396C (it) | 1899-04-01 | 1899-04-01 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE114396C (it) |
-
1899
- 1899-04-01 DE DE1899114396D patent/DE114396C/de not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE267826C (de) | Verfahren zur Darstellung von lactid | |
| DE2234474B2 (de) | Verfahren zur Herstellung fein verteilter Mikropartikel von Tyrosin mit einem Gehalt eines darin dispergierten Allergens und diese Produkte enthaltende Arzneipräparate | |
| DE1542711B2 (de) | N-phenyl-n'-oxyalkyl-n'-alkylharnstoffe, ihre verwendung als herbizide und diese enthaltende herbizide mittel | |
| DE2440633C3 (de) | 1,2-Bis-(2-oxo-pyrrolidin-l )essigsäurehydrazid, Verfahren zu seiner Herstellung und diese Verbindung enthaltende Arzneimittel | |
| DE2134085C3 (de) | Spiramycin-hydrazone | |
| DE2527157C2 (de) | Verfahren zur Herstellung von 2-Formylchinoxalin-N↑1↑,N↑4↑-dioxyddimethylacetal | |
| DE1055287B (de) | Pflanzenbekaempfungsmittel | |
| DE672494C (de) | Verfahren zur Herstellung von Hexamethylentetraminpraeparaten | |
| DE102014003082A1 (de) | Emulgierbare oder selbstemulgierende Zusammensetzung | |
| DE2121957B2 (de) | Diurethane sowie diese enthaltende herbizide Mittel | |
| DE937049C (de) | Verfahren zur Herstellung von therapeutisch wirksamen Salzen von Verbindungen der Streptomycinreihe | |
| DE964496C (de) | Verfahren zur Wiedergewinnung des bei der Herstellung von Cyclotrimethylentrinitramin anfallenden Formaldehyd- und Salpetersaeureueberschusses | |
| AT232195B (de) | Verfahren zur Herstellung von wasserlöslichen, neutrale Lösungen ergebenden Derivaten von Tetracyclinen | |
| DE575927C (de) | Verfahren zur Herstellung von Kunstmassen aus Casein unter Zugabe formaldehydabspaltender Stoffe | |
| DE657129C (de) | Verfahren zur Herstellung von Loesungen oder Extrakten aus Bakterien, Pollen oder sonstigen pflanzlichen Zellen | |
| CH527159A (de) | Verfahren zur Herstellung neuer quaternärer Ammoniumsalze | |
| AT212491B (de) | Verfahren zur Herstellung eines gereinigten Lipoids | |
| DE942509C (de) | Verfahren zur Herstellung von Estern der Nicotionsaeure | |
| DE1059464B (de) | Verfahren zur Herstellung von Barbitursaeurederivaten | |
| DE895672C (de) | Insecticides und fungicides Pflanzenschutzmittel und Verfahren zu seiner Herstellung | |
| DE964776C (de) | Verfahren zur Herstellung des Streptomycin-isonicotinsaeurehydrazon-N-oxyds und seiner Salze | |
| DE854071C (de) | Verfahren zur Wachstumsbeschleunigung von Penicillin erzeugenden Schimmelpilzen | |
| AT233171B (de) | Verfahren zur Herstellung des neuen 18-O-Methylreserpsäuremethylesters und seiner Salze | |
| AT223740B (de) | Verfahren zur Herstellung eines gegen Hämorrhoiden wirksamen Mittels | |
| DE630467C (de) | Verfahren zur Herstellung einer wasserarmen Hartemulsion |