US122065A - Improvement in medical compounds of vegetable alkaloids - Google Patents
Improvement in medical compounds of vegetable alkaloids Download PDFInfo
- Publication number
- US122065A US122065A US122065DA US122065A US 122065 A US122065 A US 122065A US 122065D A US122065D A US 122065DA US 122065 A US122065 A US 122065A
- Authority
- US
- United States
- Prior art keywords
- alkaloids
- improvement
- medical compounds
- acid
- vegetable alkaloids
- 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
- 229930013930 alkaloid Natural products 0.000 title description 9
- 150000001875 compounds Chemical class 0.000 title description 7
- 235000013311 vegetables Nutrition 0.000 title description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 6
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 5
- 241000723346 Cinnamomum camphora Species 0.000 description 5
- 229960000846 camphor Drugs 0.000 description 5
- 229930008380 camphor Natural products 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000012261 resinous substance Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- -1 morphia Natural products 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HHBOUFYYHJJTNU-UHFFFAOYSA-N 1,3,6-thiadiazepane-2,7-dithione Chemical compound S=C1NCCNC(=S)S1 HHBOUFYYHJJTNU-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
- 239000000645 desinfectant Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
Definitions
- my said invention further consists in carbolating the aibrementionedmulphite or bisulphite by uniting with either of them, and during the formation of them, respectively, phenic" acid in the proportion of about one-tenth of one per cent. of the phenic acid.
- phenic acid may be varied to suit the exigencies of the practitioner; and my said invention further consists in camphorating the aforementioned carbolated sulphite or bisulphiteby uniting camphor or other resinous substances with it during its formation, the camphor or other gumbeing suppliedin a gaseous or sublimated state, resulting from the application of heat thereto.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
UNITED STATES PATENT @EErcE.
GEORGE W. SCOLLAY, OF NEW YORK, N. Y.
IMPROVEMENT IN MEDICAL COMPOUNDS OF VEGETABLE ALKALOIDS.
Specification forming part of Letters Patent No. 122,065, dated December 19, 1871; antedated Pecember 2, 1871.
' To all whom it may concern:
Be it known that I, GEORGE W. SGOLLAY, of St. Louis, Missouri, at present residing in the city of New York, have invented a certain new and useful Chemical Compound to be used as amedor improved therapeutic disinfectant and remedy for a certain class of diseases known in the med ical profession under the generic term of zymotic, and which includes the different forms of malarious and contagious diseases depending upon or connected with fermentative action; and my said invention consists of a medical compound composed of one or more equivalents of sulphurous acid (S0 united with any of the nitrogenous vegetable alkaloids, such as morphia, strychnia,
quinia, &c., or ammonia and its derivatives, thus forming either a sulphite or a bisulphite of the alkaloids; and my said invention further consists in carbolating the aibrementionedmulphite or bisulphite by uniting with either of them, and during the formation of them, respectively, phenic" acid in the proportion of about one-tenth of one per cent. of the phenic acid. This proportion of phenic acid, however, may be varied to suit the exigencies of the practitioner; and my said invention further consists in camphorating the aforementioned carbolated sulphite or bisulphiteby uniting camphor or other resinous substances with it during its formation, the camphor or other gumbeing suppliedin a gaseous or sublimated state, resulting from the application of heat thereto.
In the formation of this compound I proceed as follows I first put the alkaloid salts in a close receiver and add ten chemical equivalents of water. I then ignite the sulphur in the sulphurburner, thus producing sulphurous gas, (80
which passes over to the close receiver containing the alkaloids, thus uniting the alkaloids and acid in the water and forming the sulphite or bisulphite, according to the proportions of acid taken up. Now, during this process the proper quantity of phenic acid is suspended in a separate receiver located in the flue of the sulphur phor in the vessel containing the phenic acid, the
camphor melting in the acid and going over with it upon the application of heat thereto.
In place of the camphor, other resinous substances or gums may be used, or such of the essential oils as may be suitable for the purpose proposed. Y
Having now described the nature and extent of my invention, I claim as new herein, and desire to secure by Letters Patent- 1. The chemical compound consisting of the sulphite or bisulphite of the vegetable alkaloids, or their equivalents.
2. Ihe chemical compound consisting of the carbolated sulphite or bisulphite of the vegeta.
ble alkaloids, or of any of the alkalies.
3. The chemical compound consisting of the carbolated sulphite or bisulphite of vegetable alkaloids, or of any of the alkalies, combined with camphor or other resinous substance, gums,
or the essential oils. 4 l
GEORGE W. SGOLLAY.
Witnesses:
PETER D. KENNY Amos BRoADNAx. (98)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US122065A true US122065A (en) | 1871-12-19 |
Family
ID=2191505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US122065D Expired - Lifetime US122065A (en) | Improvement in medical compounds of vegetable alkaloids |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US122065A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100148676A1 (en) * | 2008-12-12 | 2010-06-17 | Microchip Technology Incorporated | Three-color rgb led color mixing and control by variable frequency modulation |
-
0
- US US122065D patent/US122065A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100148676A1 (en) * | 2008-12-12 | 2010-06-17 | Microchip Technology Incorporated | Three-color rgb led color mixing and control by variable frequency modulation |
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