US812631A - Ether mixture for disinfecting. - Google Patents
Ether mixture for disinfecting. Download PDFInfo
- Publication number
- US812631A US812631A US18987604A US1904189876A US812631A US 812631 A US812631 A US 812631A US 18987604 A US18987604 A US 18987604A US 1904189876 A US1904189876 A US 1904189876A US 812631 A US812631 A US 812631A
- Authority
- US
- United States
- Prior art keywords
- disinfecting
- alcohol
- compound
- grams
- ether mixture
- 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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title description 6
- 230000000249 desinfective effect Effects 0.000 title description 3
- 239000000203 mixture Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- 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 2
- 241000723346 Cinnamomum camphora Species 0.000 description 2
- 244000166124 Eucalyptus globulus Species 0.000 description 2
- WZUVPPKBWHMQCE-UHFFFAOYSA-N Haematoxylin Chemical compound C12=CC(O)=C(O)C=C2CC2(O)C1C1=CC=C(O)C(O)=C1OC2 WZUVPPKBWHMQCE-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229960000846 camphor Drugs 0.000 description 2
- 229930008380 camphor Natural products 0.000 description 2
- 239000000645 desinfectant Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000005245 nitryl group Chemical group [N+](=O)([O-])* 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- 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
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000896693 Disa Species 0.000 description 1
- 235000004692 Eucalyptus globulus Nutrition 0.000 description 1
- 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
- 241001465754 Metazoa Species 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 238000005899 aromatization reaction Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000659 freezing mixture Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/14—Alkali metal chlorides; Alkaline earth metal chlorides
Definitions
- ()ur invention refers to a new compound which possesses special properties for deodorizing and aromatizing petroleum and other hydrocarbons.
- the resulting compound retains its properties under any condition of temperature and keeps indefinitely without any deterioration. It is also to be noted that it does not prejudicially affect any of the other roperties of petroleum nor of alcohol. Neit or does it leave any residuum after combustion. In its manufacture we use dehydrated sea-salt on account of the very small cost of the same, while it contains the chlorids, bromids, and sulfates of sodium, potassium, calcium, and magnesiumwhich we require to utilize; but we might employ any of the com ounds containing the above-mentioned su stances or components for the pur ose of extracting from the same the materials which compose our compound.
- the acetate of ammonia is employed as a vfifteen per millimeter of our compound.
- the mcthylic, ethylic, and amylic alcohols acidulatcd with hydrochloric acid for the purpose of forming the ether compounds appertaining to the different compounds, and, finally, the bidoxid of nitrogen to the end that it may intervene in the formation of the nitryls and aldehydes, which are oxidizing and disinfecting agents, specially those of mcthylic alcohol, the antiseptic pIopcrties of which are well known.
- the eucalyptus and camphor contribute to avoid any isagreeable emanations during the combustion of the h drocarbons, apart from the advantages to be derived from the well-known balsamic and hygienic properties of those ingredients.
- the kerosene treated in this manner becomes suitable for the employment in the manufacture of varnishes through the increase which takes place in its siccative power and the elimination of all disa reeable odor.
- the operation of denatural izing alcohol consists merely of adding to the same ten go 13 may be colored with any of the usual substances or with eosin, hematoxylin, carmine fuchsin, orpicric acid in any of its various combinations.
- the alcohol thus treated is 'unfit to be taken into the stomach; but its strong, but not disagreeable, odor effectively prevents all possibiht of mistake. It should also be pointed out t lat it loses none of the I properties which render it available for other industrial and domestic uses.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
UN .lTEl) i TAT ES TUMA S l.-\l.(illCliA, JOSE l'lNZAN'l MlSlMWSKY, ALFREDO UARlCUlllIA, AN!) liUlllS lCMlLlANQ ODlU, Old BUENOS AYRES, ARGENTINA.
ETHER MIXTURE FQR DESBNFEGTENG.
Specification of Letters Patent.
Application filed January 20, 1904. Serial No. 189,876- (Spccimena) Patented Feb. 13, 1906.
a citizen of the United States of America, and
residents of N o. 590 (.falle Reconquista, in the (-Ity of Buenos Ayres, Argentina, have invented a new and useful improvement in Ether Mixtures for Disinfecting purposes, of which the following is a specification.
()ur invention refers to a new compound which possesses special properties for deodorizing and aromatizing petroleum and other hydrocarbons. 1
In the manufacture of our new compound we proceed as follows: We macerate, during lii'teen days, leaves of eucalyptus globulus, thirty grams; camphol', live grams; in unrectilied ethylic alcohol, three hundred grams; in unrectified methylic alcohol, threehundred grams; in unrectiiied amylic alcohol, three hundred grams; in commercial hydrochloric acid ,onehundred grams. Afterfifteen da s'we add dehydrated sea-salt, three hundre and eighty grams; commercial sulfuric acid, thirty-five grams; acetate of ammonia,.sixty grams. The whole is left to macerate fortyeight hours longer, after which it is submitted to distillation, the vapors heir) concentrated in a Liebig cooler, which deposits the product in a suitable receiver resting in a freezing mixture. At the same time binoxid of nitrogen is led from another generator into this receiver until the nitryls shall have formed.
The resulting compound. retains its properties under any condition of temperature and keeps indefinitely without any deterioration. It is also to be noted that it does not prejudicially affect any of the other roperties of petroleum nor of alcohol. Neit or does it leave any residuum after combustion. In its manufacture we use dehydrated sea-salt on account of the very small cost of the same, while it contains the chlorids, bromids, and sulfates of sodium, potassium, calcium, and magnesiumwhich we require to utilize; but we might employ any of the com ounds containing the above-mentioned su stances or components for the pur ose of extracting from the same the materials which compose our compound.
The acetate of ammonia is employed as a vfifteen per millimeter of our compound.
source of the production of acetic acid and of ammonia; the mcthylic, ethylic, and amylic alcohols acidulatcd with hydrochloric acid for the purpose of forming the ether compounds appertaining to the different compounds, and, finally, the bidoxid of nitrogen to the end that it may intervene in the formation of the nitryls and aldehydes, which are oxidizing and disinfecting agents, specially those of mcthylic alcohol, the antiseptic pIopcrties of which are well known. The eucalyptus and camphor contribute to avoid any isagreeable emanations during the combustion of the h drocarbons, apart from the advantages to be derived from the well-known balsamic and hygienic properties of those ingredients.
To carry out the deodoriz'ation and aroma tization of kerosene or other hydrocarbons,
it su'l'l'ices to add to the same from ten to thirty-five per millimeter of our compound, according to the quality of the article under treatment. In certain cases we may commence by adding to the kerosene not more than three per m1llimeter,'by weight, of alum and decanting after forty-eight hours and then treating the kerosene by our compound.
After the very simple treatment we have thus described it will be found that the characteristic odor of etroleum will have completely disappeared, eingreplaced by an a reeable aroma. At the same time it will be 0 served that the oil has lost some of its greasiness; that its illuminatin ower is'greater, the li ht bein clearer, w i e the flashing-point is higher, which is a: reat advantage, as the danger of accidenta ignition is thus diminished. These latter effects may be attributed to the formation of chlorids, bromids, and sulfates of the salts contained in the seasalt employed in the preparation. Furthermore, the kerosene treated in this manner becomes suitable for the employment in the manufacture of varnishes through the increase which takes place in its siccative power and the elimination of all disa reeable odor. The operation of denatural izing alcohol consists merely of adding to the same ten go 13 may be colored with any of the usual substances or with eosin, hematoxylin, carmine fuchsin, orpicric acid in any of its various combinations. The alcohol thus treated is 'unfit to be taken into the stomach; but its strong, but not disagreeable, odor effectively prevents all possibiht of mistake. It should also be pointed out t lat it loses none of the I properties which render it available for other industrial and domestic uses. Our compound when used for this purpose possesses the highl -valuable property of becoming so intimate y combined with the alcohol as to render it quite impossible to eliminate it by redistillation or by any other process whatever. So there is no danger of the alcohol ever bein used in the preparation of any article whic is to be taken into the stomach. It ma be used in the pre aration of varnishes, w 'ch will be more bri liant and dry quicker. The combustion of this alcohol produces no smoke, the products of the same being rather aromatie and disinfectant and have besides the balsamic and hygienic properties which, as is well known, euca yptus and camphor possess.
Among other purposes for which our compound may be used we may mention the arcmatization of animal fats and oils, the said agent being added in the proportion that mag be most expedient in each case.
andle-wicks may be impregnated with this substance, as the light given will be found to haveincreased brilliancy.
' Having thus described our invention, what We claim as new, and desire to secure by Letgo ters Patent, is
1. The aromatic and disinfecting compound am he alcohol, hydrochloric acid, sea-salt,
sul rie acid, acetate of ammonia and binoxid of nitrogen, in or about the proportions described.
In witness whereof we have signed our 7 names to this specification in the presence of two subscribing witnesses.
TOMAS BARGIELA. JOSE PINZANI MISLOWSKY. ALFREDO CARICCHIA. LOUIS EMILIANO ()DlO.
Witnesses:
P. A. BRENEY, AN'ro. L. Benz.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18987604A US812631A (en) | 1904-01-20 | 1904-01-20 | Ether mixture for disinfecting. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18987604A US812631A (en) | 1904-01-20 | 1904-01-20 | Ether mixture for disinfecting. |
Publications (1)
Publication Number | Publication Date |
---|---|
US812631A true US812631A (en) | 1906-02-13 |
Family
ID=2881111
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US18987604A Expired - Lifetime US812631A (en) | 1904-01-20 | 1904-01-20 | Ether mixture for disinfecting. |
Country Status (1)
Country | Link |
---|---|
US (1) | US812631A (en) |
-
1904
- 1904-01-20 US US18987604A patent/US812631A/en not_active Expired - Lifetime
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