US2185255A - Saponaceous shaving composition - Google Patents
Saponaceous shaving composition Download PDFInfo
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- US2185255A US2185255A US149096A US14909637A US2185255A US 2185255 A US2185255 A US 2185255A US 149096 A US149096 A US 149096A US 14909637 A US14909637 A US 14909637A US 2185255 A US2185255 A US 2185255A
- Authority
- US
- United States
- Prior art keywords
- parts
- shaving
- saponaceous
- substances
- lipoid
- 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
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- 239000000203 mixture Substances 0.000 title description 10
- 239000000126 substance Substances 0.000 description 47
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- 230000002439 hemostatic effect Effects 0.000 description 25
- 239000002437 shaving preparation Substances 0.000 description 25
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 24
- 239000000344 soap Substances 0.000 description 19
- 238000001179 sorption measurement Methods 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- 244000068988 Glycine max Species 0.000 description 16
- 235000010469 Glycine max Nutrition 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 15
- 239000008280 blood Substances 0.000 description 13
- 210000004369 blood Anatomy 0.000 description 13
- 235000019441 ethanol Nutrition 0.000 description 13
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 235000021355 Stearic acid Nutrition 0.000 description 12
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 12
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 241000283973 Oryctolagus cuniculus Species 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 239000008117 stearic acid Substances 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 10
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000003208 petroleum Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000005345 coagulation Methods 0.000 description 7
- 230000015271 coagulation Effects 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000003925 fat Substances 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 235000013162 Cocos nucifera Nutrition 0.000 description 5
- 244000060011 Cocos nucifera Species 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 238000005194 fractionation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 235000011118 potassium hydroxide Nutrition 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 235000013311 vegetables Nutrition 0.000 description 4
- 102000007625 Hirudins Human genes 0.000 description 3
- 108010007267 Hirudins Proteins 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229940030225 antihemorrhagics Drugs 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000002874 hemostatic agent Substances 0.000 description 3
- WQPDUTSPKFMPDP-OUMQNGNKSA-N hirudin Chemical compound C([C@@H](C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C=CC(OS(O)(=O)=O)=CC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H]1NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H]2CSSC[C@@H](C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)N[C@H](C(NCC(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N2)=O)CSSC1)C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]1NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=2C=CC(O)=CC=2)NC(=O)[C@@H](NC(=O)[C@@H](N)C(C)C)C(C)C)[C@@H](C)O)CSSC1)C(C)C)[C@@H](C)O)[C@@H](C)O)C1=CC=CC=C1 WQPDUTSPKFMPDP-OUMQNGNKSA-N 0.000 description 3
- 229940006607 hirudin Drugs 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 3
- 239000001814 pectin Substances 0.000 description 3
- 235000010987 pectin Nutrition 0.000 description 3
- 229920001277 pectin Polymers 0.000 description 3
- -1 petrol Chemical compound 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 241000416162 Astragalus gummifer Species 0.000 description 2
- 101000993302 Hirudo medicinalis Hirudin variant-1 Proteins 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 229920001615 Tragacanth Polymers 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000010466 nut oil Substances 0.000 description 2
- ONQDVAFWWYYXHM-UHFFFAOYSA-M potassium lauryl sulfate Chemical compound [K+].CCCCCCCCCCCCOS([O-])(=O)=O ONQDVAFWWYYXHM-UHFFFAOYSA-M 0.000 description 2
- 229940116985 potassium lauryl sulfate Drugs 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000000196 tragacanth Substances 0.000 description 2
- 235000010487 tragacanth Nutrition 0.000 description 2
- 229940116362 tragacanth Drugs 0.000 description 2
- SRXWLOLJJPXKDX-UHFFFAOYSA-N 10-[(1-methylpiperidin-2-yl)methyl]phenothiazine Chemical compound CN1CCCCC1CN1C2=CC=CC=C2SC2=CC=CC=C21 SRXWLOLJJPXKDX-UHFFFAOYSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229910052936 alkali metal sulfate Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/38—Products in which the composition is not well defined
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S128/00—Surgery
- Y10S128/22—Blood coagulation
Definitions
- ceous shaving preparations, respectively, inaccordance with the invention are remarkable for their excellent lathering power.
- Razors readily produce cuts of the skin and consequently causebleeding. With a view to stop ping said bleeding, in accordance with the present invention there are added to the shaving soaps or saponaceous shaving preparations, respectively, styptic or hemostatic substances.
- a number of substances promoting the coagulation of blood are known per se. These substances, however, are not readily suitable as an addition to shaving soaps. In selecting styptic or hemostatic substances which are to be added to shaving soaps, care must be taken that they do not impair the lathering power of said shaving soaps.
- This invention then has as an object new shaving soaps or saponaceous shaving preparations, respectively, and methods for their production.
- a further object is shaving soaps or saponaceous shaving preparations, respectively, possessing excellent lathering power.
- a still further object is shaving soaps or saponaceous shaving preparations, respectively, containing an addition of styptic or hemostatic substances which will not impair the said lathering power. 7
- lipoid soluble substances from soybeans contain agents which act as styptics or hemostatics.
- the term lipoid soluble substances is used in the present specification and claims to mean substances which are soluble in the usual solvents for fats, such as ether.
- the aforementioned lipoid soluble substances from soybeans contain, in addition to compounds acting as styptics or hemostatics, other compounds which are extensively inactive in this respect. Therefore, it is unsuitable to add to the shaving soaps the lipoid soluble substances from soybeans as a. whole, particularly in view of the fact that an excessive amount of lipoid soluble substances from soybeans will unfavourably affect the lathering power of the shaving soap or saponaceous shaving preparations, respectively.
- fractionation is effected by treating the said substances with selective solvents.
- fractionation may proceed in the re verse order, i. e., by adding another solvent will be precipitated the styptic or hemostatic substances, while the less active components remain in solution.
- adding e. g., ethyl alcohol to a petroleum ether solution of the lipoid soluble substances from soybeans, there will be precipitated the less active components.
- acetone to a solution of the lipoid soluble substances from soybeans in ether, petrol, or benzene, precipitation of the styptic or hemostatic substances will be effected.
- Fractionation may be carried'out repeatedly if desired, e. g., in such away that thelast mentioned precipitate obtained by adding acetone to ethereal solutions is redissolved in ether and again precipitated with acetone or alcohol.
- the concentration of the styptic or hemostatic substances is checked by physiological tests. Fractionation is continued until a. preparation is obtained, .1 cc. of a 1% solution of which will coagulate 1 cc. of rabbit blood which has previously been. admixed with hirudin in the ratio 127500, after one hour. Hirudin blood without addition of the lipoid fraction will coagulate after 48 hours.
- the new shaving soaps or saponaceous shaving preparations, respectively, according to the present invention containfrom about 3 to 10% of, the styptic or hemostatic substances obtained from soybeans. An addition of 5% has proved particularly advantageous. These styptic or he- -mostatic substances when added to shaving soaps, without impairing their lathering power, will cause bleeding from small cuts to stop immediately.
- Another embodiment of the invention consists in adding to the shaving soaps or saponaceous shaving preparations, respectively, the, styptic or hemostatic substances in the form of adsorption compounds upon carriers, such as calcium carbonate, aluminium oxide, or silica.
- adsorption compounds are obtained by stirring aqueous emulsions, or solutions in organic solvents, of the styptic or hemostatic substances with the said adsorbents, and removing the supernatant liquid as soon as adsorption is complete.
- 2' parts of adsorbent will be used for 1 part of the styptic or hemostatic 'substances.
- the adsorption compounds show a considerably increased activity, as compared with the'parent material. Although the active substance amounts to one third only of the adsorption compounds, in most cases it will be suflicient to add to the soap 340% of said adsorption compound.
- the shaving soaps in accordance with the present invention to contain, in addition, certain amounts of free organic acids. These acids will effect a considerable more intimate combination of the I lipoid soluble substances with the soap mass and, in the case of cream-like products, will prevent separation of the watery constituents.
- high molecular fatty acids such as stearic and palmitic acid, and/or aliphatic hydroxy acids such as citric, tartaric, or lactic acid,
- mucous substances such as tragacanth, and particularly pectin substances which may be obtained, e. g. from unripe fruits.
- soap-like products such as the alkali metal sulfates or sulfonates of high molecular fatty alcohols come likewise within the scope of the present invention.
- soap-like products such as the alkali metal sulfates or sulfonates of high molecular fatty alcohols come likewise within the scope of the present invention.
- sodium lauryl sulfonate may be cited.
- the shaving soaps or saponaceous shaving preparations, respectively, according to the invention may contain all the various admixtures mentioned above, alone as well'as in combination. Our invention is illustrated but not limited by the following examples. 80
- the fractionating of the lipoid soluble substances can be illustrated as follows:
- Example I 100 kg. of soybeans were broken up by means of a crusher and extracted with petroleum ether until exhausted. By concentrating the petroleum ether solution to a strength of 20%, there were obtained 80 litres of this extract. Four times the amount of acetone was added thereto and the 4 whole was subjected to centrifugation. After removal of the solvent the precipitate amounted to 1.7 kg. It was redissolved in 8 litresof petroleum ether and precipitated with 20 litres of alcohol. There were obtained .8 kg. of a-substance soluble in alcohol, and .9 kg. of a substance insoluble in alcohoh The amounts of styptic or hemostat'ic substances contained in the various fractions were determined by means of the following coagulation tests:
- Example II 1000. of rabbit blood (with hirudin l:7500) No coagulation after 48 hours. 10 cc. of rabbit blood (with hirudin 1:7500) +.1 cc. Coagulation after oill7f aqueous solution of vegetable lipoid (al- 35 minutes. co 0 soluble fraction). 10 cc. of rabbit blood (with himdin l: 7500) +.l cc. Coagulation after 20 minutes.
- Example III 25 g. of the'alcohol soluble fraction in accordance with Example I were colloidally dispersed n 100 cc. of water and admixed with g. of calcium carbonate. The adsorption product was separated from the aqueous solution by centrifugation, and dried. When subjected to thecoagulation test it gave results which were in concordance with those of Example II.
- Example IV 25 g. of the alcohol soluble fraction in accordance with Example I were colloidally dispersed in 100 cc. of water and admixed with '75 g. of silica. The adsorption product was separated from the liquid by centrifugation, and dried. When subcoagulation test it gave results which were in concordance with those of Example II.
- Example V together 5 parts of the lipoid fraction obtained in accordance with Example I, and the mixture was added to the saponification mass.
- the product thus obtained can be worked up to form shaving sticks.
- Upon addition of 50 parts of water a cream-like product will be obtained theref,
- Example VI parts of stearic acid, 10 parts of cocoanut oil fatty acid were saponified by means of 20.6 parts of KOH in 34 parts of mo and exactly neutralized. In the meantime there were melted together 5 parts of stearic acid lipoid adsorption product according to Example II, and the mixture was added to the saponlflca obtained can be worked up to form shaving sticks. Upon addition of 50 parts of water obtained therefrom.
- Example VII 92 parts of potassium lauryl sulfate containinr a minimum of electrolytes, 27 parts of cetyl aloe-- and 10 parts of the acream-like product will be hol, and 1 part of lactic acid, were admixed with 100 parts of water. To this mixture there was added, while heating, a mixture comprising parts of the lipoid adsorption product according to Example IV and 5 parts of stcaric acid, until a product of paste-like consistency was formed.
- Example VH1 90 parts of stearic acid, parts of cocoanut oil fatty acid were saponified by means of 20.6 parts KOH (dissolved in 34 parts of water), and exactly neutralized. To this mixture there were added 10 parts of the lipoid adsorption produ t according to Example 111 which had previously been melted together with 5- parts of stearic acid. Finally, 100 parts of a 2% paste of tragacanth. pectin, or other vegetable mucous substances were added to the mass.
- hemostatic in the appended claims to include agents which possess hemostatic or styptic qualities.
- saponaceous used to include soap-like material, whether a true soap or another chemical compound having suitable lathering properties.
- a saponaceous shaving preparation containing a hemostatic lipoid-soluble substance which has been derived from soy-beans by dissolving constituents of the soy-beans in a water-immiscible fat solvent from the group consisting of petroleum ether, ether, benzine and benzol, adding a water-miscible fat solvent from the group consisting of ethyl alcohol and acetone to the solution, and recovering the lipoid-soluble substance from the resulting materials.
- a saponaceous shaving preparation contain ing a hemostatic lipoid-soluble substance which has been derived from soy-beans by dissolution in a water-immiscible tat solvent from the group consisting of petroleum benzol, and separation oi! the more effective constituents by the addition or acetone.
- ether, ether, benzine and ble fat solvent from the group consisting of petroleum ether, ether, benzine and benzol, adding a water-miscible fat solvent from the group consisting of ethyl alcohol and acetone to the solution, and recovering the lipoid-soluble substance from the resulting materials, said substance being present in the preparation in the amount of about 3 to 10%, by weight.
- a saponaceous shaving preparation as claimed in claim I which contains the hemostatic substance in the form of adsorption compounds upon an inorganic carrier.
- a saponaceous shaving preparation as claimed in claim 1 which comprises about 90 parts of stearic acid, 10 parts of cocoanut oil fatty acid, the amount of caustic potash-required for neutralization, and 10 parts of a mixture consisting of 5 parts of stearic acid and 5 parts of said hemostatic substance, all parts by weight.
- a saponaceous shaving preparation as claimed in claim 1 which comprises, by weight, about 92 parts of potassium lauryl sulfate, 27 parts'of cetylalcohol, 1 part of lacetic acid, 10 parts of a. mixture consisting of 5 parts of stearic acid and 5 parts of compound consisting of said hemostatic substances in adsorption upon silica HUGO KRfiPER. IRICE 'I'HOMAE
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- Medicinal Preparation (AREA)
Description
2,185,255 SAPQNACEOUS 5G CG GSGlN Hugo Kriiper,
Stuttgart, Germany,
Hamburg, and Erich Thor-nae,
assignors to the h:
Chemische Fabriir. Promonta G. m. b. 15in Elamburg, Germany, a company or Genny No man's. Application time is, was,
Serial No. mp9s i3 ii'llaims.
ceous shaving preparations, respectively, inaccordance with the invention are remarkable for their excellent lathering power.
Razors readily produce cuts of the skin and consequently causebleeding. With a view to stop ping said bleeding, in accordance with the present invention there are added to the shaving soaps or saponaceous shaving preparations, respectively, styptic or hemostatic substances.
A number of substances promoting the coagulation of blood are known per se. These substances, however, are not readily suitable as an addition to shaving soaps. In selecting styptic or hemostatic substances which are to be added to shaving soaps, care must be taken that they do not impair the lathering power of said shaving soaps.
This invention then has as an object new shaving soaps or saponaceous shaving preparations, respectively, and methods for their production. A further object is shaving soaps or saponaceous shaving preparations, respectively, possessing excellent lathering power. A still further object is shaving soaps or saponaceous shaving preparations, respectively, containing an addition of styptic or hemostatic substances which will not impair the said lathering power. 7
We have. found that the lipoid soluble substances from soybeans contain agents which act as styptics or hemostatics. The term lipoid soluble substances" is used in the present specification and claims to mean substances which are soluble in the usual solvents for fats, such as ether. The aforementioned lipoid soluble substances from soybeans contain, in addition to compounds acting as styptics or hemostatics, other compounds which are extensively inactive in this respect. Therefore, it is unsuitable to add to the shaving soaps the lipoid soluble substances from soybeans as a. whole, particularly in view of the fact that an excessive amount of lipoid soluble substances from soybeans will unfavourably affect the lathering power of the shaving soap or saponaceous shaving preparations, respectively.
By fractionating the lipoid soluble substances from soybeans we obtain. products which possess considerably increased stypticor hemostatic properties. according to the invention fractionation is effected by treating the said substances with selective solvents. In certain cases, by adding another solvent to the solution of ali the lipoid soluble constituents of soybeans, there he precipitated the less active components. On other hand, fractionation may proceed in the re verse order, i. e., by adding another solvent will be precipitated the styptic or hemostatic substances, while the less active components remain in solution. By adding, e. g., ethyl alcohol to a petroleum ether solution of the lipoid soluble substances from soybeans, there will be precipitated the less active components. 0n. the other hand, by adding acetone to a solution of the lipoid soluble substances from soybeans in ether, petrol, or benzene, precipitation of the styptic or hemostatic substances will be effected.
Fractionation may be carried'out repeatedly if desired, e. g., in such away that thelast mentioned precipitate obtained by adding acetone to ethereal solutions is redissolved in ether and again precipitated with acetone or alcohol.
The concentration of the styptic or hemostatic substances is checked by physiological tests. Fractionation is continued until a. preparation is obtained, .1 cc. of a 1% solution of which will coagulate 1 cc. of rabbit blood which has previously been. admixed with hirudin in the ratio 127500, after one hour. Hirudin blood without addition of the lipoid fraction will coagulate after 48 hours.
The new shaving soaps or saponaceous shaving preparations, respectively, according to the present invention containfrom about 3 to 10% of, the styptic or hemostatic substances obtained from soybeans. An addition of 5% has proved particularly advantageous. These styptic or he- -mostatic substances when added to shaving soaps, without impairing their lathering power, will cause bleeding from small cuts to stop immediately.
Another embodiment of the invention consists in adding to the shaving soaps or saponaceous shaving preparations, respectively, the, styptic or hemostatic substances in the form of adsorption compounds upon carriers, such as calcium carbonate, aluminium oxide, or silica.
These adsorption compounds are obtained by stirring aqueous emulsions, or solutions in organic solvents, of the styptic or hemostatic substances with the said adsorbents, and removing the supernatant liquid as soon as adsorption is complete. As a rule, 2' parts of adsorbent will be used for 1 part of the styptic or hemostatic 'substances. The adsorption compounds show a considerably increased activity, as compared with the'parent material. Although the active substance amounts to one third only of the adsorption compounds, in most cases it will be suflicient to add to the soap 340% of said adsorption compound.
the shaving soaps in accordance with the present invention to contain, in addition, certain amounts of free organic acids. These acids will effect a considerable more intimate combination of the I lipoid soluble substances with the soap mass and, in the case of cream-like products, will prevent separation of the watery constituents. In thisconnection, high molecular fatty acids such as stearic and palmitic acid, and/or aliphatic hydroxy acids such as citric, tartaric, or lactic acid,
may be employed.
Similarly, it is an advantage to add to the shavlug soaps or saponaceous shaving preparations, respectively, according to the invention mucous substances such as tragacanth, and particularly pectin substances which may be obtained, e. g. from unripe fruits.
Preparations which, in lieu of soaps, contain soap-like products, such as the alkali metal sulfates or sulfonates of high molecular fatty alcohols come likewise within the scope of the present invention. As an example of this type of compounds, sodium lauryl sulfonate may be cited.
The shaving soaps or saponaceous shaving preparations, respectively, according to the invention, may contain all the various admixtures mentioned above, alone as well'as in combination. Our invention is illustrated but not limited by the following examples. 80 The fractionating of the lipoid soluble substances can be illustrated as follows:
Example I 100 kg. of soybeans were broken up by means of a crusher and extracted with petroleum ether until exhausted. By concentrating the petroleum ether solution to a strength of 20%, there were obtained 80 litres of this extract. Four times the amount of acetone was added thereto and the 4 whole was subjected to centrifugation. After removal of the solvent the precipitate amounted to 1.7 kg. It was redissolved in 8 litresof petroleum ether and precipitated with 20 litres of alcohol. There were obtained .8 kg. of a-substance soluble in alcohol, and .9 kg. of a substance insoluble in alcohoh The amounts of styptic or hemostat'ic substances contained in the various fractions were determined by means of the following coagulation tests:
Coazulated alter M A. Subdcncc soluble in acetone .1 cc. of 17 ageous solution +1.0 cc. of rabbit blood with irudin 1:1500 10 hours. .1 cc. of 7, a ucous solution +1.0 cc. of rabbit blood th irudin 1:7500 No reaction after 10 hours. B. 3mm mum in alcohol .1 cc. cl 1% a ueous solution +1.0 cc. of rabbit blood with irudin 1:750 0 1 hour.
.1 cc. ol .3% a ueous solution +1.0 cc. of rabbit blood with irudin 1:7500 Do. l 0. Substance imoluble in alcohol .1 cc. of 1% 5%100118 solution +1.0 cc. of rabbit blood with irudin 1:7500 2% hours. .1 cc. of 3% a%ieous solution +1.0 cc. of rabbit blood with irudin 1:7500 10 hours.
These tests show that the substance soluble in alcohol is the most eflective agent in promoting coagulation.
An example of the preparation of the adsorption compound upon aluminium oxide is as follows:
. jected to the tion mass. The product thus Example II 1000. of rabbit blood (with hirudin l:7500) No coagulation after 48 hours. 10 cc. of rabbit blood (with hirudin 1:7500) +.1 cc. Coagulation after oill7f aqueous solution of vegetable lipoid (al- 35 minutes. co 0 soluble fraction). 10 cc. of rabbit blood (with himdin l: 7500) +.l cc. Coagulation after 20 minutes.
of 1% aqueous solution of vegetable lipoid (alcohol soluble fraction) +7% aluminum oxide.
Coagulation after 24 hours.
10 cc. of rabbit blood (with hirudin 1:7500) +.l cc.
of 7% aluminum oxide in water.
The following example illustrates the preparation of the adsorption compound upon calcium carbonate:
Example III 25 g. of the'alcohol soluble fraction in accordance with Example I were colloidally dispersed n 100 cc. of water and admixed with g. of calcium carbonate. The adsorption product was separated from the aqueous solution by centrifugation, and dried. When subjected to thecoagulation test it gave results which were in concordance with those of Example II.
The following example illustrates the preparation of the adsorption compoundupon silica:
Example IV 25 g. of the alcohol soluble fraction in accordance with Example I were colloidally dispersed in 100 cc. of water and admixed with '75 g. of silica. The adsorption product was separated from the liquid by centrifugation, and dried. When subcoagulation test it gave results which were in concordance with those of Example II.
As a practical illustration of the production of shaving preparations in accordance with the present invention the following examples, in which the parts are by weight, are given:
Example V together 5 parts of the lipoid fraction obtained in accordance with Example I, and the mixture was added to the saponification mass. The product thus obtained can be worked up to form shaving sticks. Upon addition of 50 parts of water a cream-like product will be obtained theref,
Example VI parts of stearic acid, 10 parts of cocoanut oil fatty acid were saponified by means of 20.6 parts of KOH in 34 parts of mo and exactly neutralized. In the meantime there were melted together 5 parts of stearic acid lipoid adsorption product according to Example II, and the mixture was added to the saponlflca obtained can be worked up to form shaving sticks. Upon addition of 50 parts of water obtained therefrom.
Example VII 92 parts of potassium lauryl sulfate containinr a minimum of electrolytes, 27 parts of cetyl aloe-- and 10 parts of the acream-like product will be hol, and 1 part of lactic acid, were admixed with 100 parts of water. To this mixture there was added, while heating, a mixture comprising parts of the lipoid adsorption product according to Example IV and 5 parts of stcaric acid, until a product of paste-like consistency was formed.
Example VH1 90 parts of stearic acid, parts of cocoanut oil fatty acid were saponified by means of 20.6 parts KOH (dissolved in 34 parts of water), and exactly neutralized. To this mixture there were added 10 parts of the lipoid adsorption produ t according to Example 111 which had previously been melted together with 5- parts of stearic acid. Finally, 100 parts of a 2% paste of tragacanth. pectin, or other vegetable mucous substances were added to the mass.
We employ the word hemostatic in the appended claims to include agents which possess hemostatic or styptic qualities. term saponaceous used to include soap-like material, whether a true soap or another chemical compound having suitable lathering properties. In setting forth particular ingredients of the improved shaving preparations and particular quantities or proportions thereof we recognize that wide variations may be made without sacrificing advantages of our invention, and we therefore desire that the claims be accorded a scope fully commensurate with the spirit of the invention and its departure from the prior art.
We claim:
1. .A saponaceous shaving preparation containing a hemostatic lipoid-soluble substance which has been derived from soy-beans by dissolving constituents of the soy-beans in a water-immiscible fat solvent from the group consisting of petroleum ether, ether, benzine and benzol, adding a water-miscible fat solvent from the group consisting of ethyl alcohol and acetone to the solution, and recovering the lipoid-soluble substance from the resulting materials.
2. A saponaceous shaving preparation containing a hemostatic lipoid-solublc substance which has been derived from soy-beans by dissolution in a water-immiscible fat solvent from the group consisting of petroleum ether, ether, benzlne and benzol and separation of the less efiective cons'tituents by precipitation with ethyl alcohol.
3. A saponaceous shaving preparation contain ing a hemostatic lipoid-soluble substance which has been derived from soy-beans by dissolution in a water-immiscible tat solvent from the group consisting of petroleum benzol, and separation oi! the more effective constituents by the addition or acetone.
4. A saponaceous shaving preparation containing a hemostatic lipoid-soluble substance which has been derived from soy-beans by dissolving constituents of the soy-beans in a water-immisci- Similarly, the
ether, ether, benzine and ble fat solvent from the group consisting of petroleum ether, ether, benzine and benzol, adding a water-miscible fat solvent from the group consisting of ethyl alcohol and acetone to the solution, and recovering the lipoid-soluble substance from the resulting materials, said substance being present in the preparation in the amount of about 3 to 10%, by weight.
5. A saponaceous shaving preparation as claimed in claim 1, which contains the hemo static substance in the amount of about 5%, by weight.
6. A saponaceous shaving preparation as claimed in claim I, which contains the hemostatic substance in the form of adsorption compounds upon an inorganic carrier.
7. A saponaceous shaving preparation as claimed in claim 1, which in addition contains free high molecular fatty acids.
8. A saponaceous shaving preparation as claimed in claim 1, which in addition contains an aliphatic hydroxy acid selected from the group consisting of tartaric, citric, and lactic acids.
9. A- saponaceous shaving preparation as claimed in claim 1, which in addition contains water soluble vegetable mucous substance.
10. A saponaceous shaving preparation as claimed in claim 1, which comprises about 90 parts of stearic acid, 10 parts of cocoanut oil fatty acid, the amount of caustic potash-required for neutralization, and 10 parts of a mixture consisting of 5 parts of stearic acid and 5 parts of said hemostatic substance, all parts by weight.
11. A saponaceous shaving preparation as claimed in claim 1, which comprises, by weight,
about 90 parts of stearic acid, 10 parts of cocoa nut oil fatty acldfthe amount of caustic potash required for neutralization, and parts of a mixture consisting of about 5 parts of stearic acid and 10 parts of compound consisting of said hemostatic substances in adsorption upon aluminum oxide.
l2. A saponaceous shaving preparation as claimed in claim 1, which comprises, by weight, about 90 parts of stearic acid, 10 parts of cocoa nut oil fatty acid, the amount of caustic potash required for neutralization, 100 parts or a 2% paste of pectin, and 10 parts of a mixture consisting of 5 parts of stearic acid and 5 parts of compound consisting of said hemostatic substances in adsorption upon calcium carbonate.
13. A saponaceous shaving preparation as claimed in claim 1, which comprises, by weight, about 92 parts of potassium lauryl sulfate, 27 parts'of cetylalcohol, 1 part of lacetic acid, 10 parts of a. mixture consisting of 5 parts of stearic acid and 5 parts of compound consisting of said hemostatic substances in adsorption upon silica HUGO KRfiPER. IRICE 'I'HOMAE
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1937C0052885 DE693027C (en) | 1937-06-02 | 1937-06-02 | Shaving soap and preparations |
| US149096A US2185255A (en) | 1937-06-19 | 1937-06-19 | Saponaceous shaving composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US149096A US2185255A (en) | 1937-06-19 | 1937-06-19 | Saponaceous shaving composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2185255A true US2185255A (en) | 1940-01-02 |
Family
ID=22528785
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US149096A Expired - Lifetime US2185255A (en) | 1937-06-02 | 1937-06-19 | Saponaceous shaving composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2185255A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2642375A (en) * | 1951-08-21 | 1953-06-16 | Ethicon Suture Lab Inc | Hemostatic compositions |
| US3071510A (en) * | 1958-06-05 | 1963-01-01 | Dome Chemicals Inc | Protein-tar acid dermatological preparation |
| US4647394A (en) * | 1981-04-07 | 1987-03-03 | Mitsubishi Chemical Industries Limited | Soap composition |
| US20080119380A1 (en) * | 2004-12-09 | 2008-05-22 | Kyoko Okada | Cleansing Agent |
-
1937
- 1937-06-19 US US149096A patent/US2185255A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2642375A (en) * | 1951-08-21 | 1953-06-16 | Ethicon Suture Lab Inc | Hemostatic compositions |
| US3071510A (en) * | 1958-06-05 | 1963-01-01 | Dome Chemicals Inc | Protein-tar acid dermatological preparation |
| US4647394A (en) * | 1981-04-07 | 1987-03-03 | Mitsubishi Chemical Industries Limited | Soap composition |
| US20080119380A1 (en) * | 2004-12-09 | 2008-05-22 | Kyoko Okada | Cleansing Agent |
| EP1840200A4 (en) * | 2004-12-09 | 2008-06-04 | Kao Corp | Cleansing agent |
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