US2271409A - Phosphatidic composition - Google Patents
Phosphatidic composition Download PDFInfo
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- US2271409A US2271409A US311705A US31170539A US2271409A US 2271409 A US2271409 A US 2271409A US 311705 A US311705 A US 311705A US 31170539 A US31170539 A US 31170539A US 2271409 A US2271409 A US 2271409A
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- phosphate
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- 239000000203 mixture Substances 0.000 title description 32
- 150000001875 compounds Chemical class 0.000 description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 150000001340 alkali metals Chemical class 0.000 description 22
- 229910052783 alkali metal Inorganic materials 0.000 description 21
- 239000000047 product Substances 0.000 description 20
- 239000001488 sodium phosphate Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- 229910019142 PO4 Inorganic materials 0.000 description 9
- 240000008042 Zea mays Species 0.000 description 9
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 9
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 9
- 235000005822 corn Nutrition 0.000 description 9
- 235000021317 phosphate Nutrition 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 7
- 235000010469 Glycine max Nutrition 0.000 description 7
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 7
- 235000011008 sodium phosphates Nutrition 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 6
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 6
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 6
- 229910000162 sodium phosphate Inorganic materials 0.000 description 6
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 6
- 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 5
- 239000000463 material Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 229960004488 linolenic acid Drugs 0.000 description 3
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 235000012343 cottonseed oil Nutrition 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- 150000004712 monophosphates Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000013310 margarine Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229940100662 nasal drops Drugs 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229940083466 soybean lecithin Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
- 238000009489 vacuum treatment Methods 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/10—Phosphatides, e.g. lecithin
- C07F9/103—Extraction or purification by physical or chemical treatment of natural phosphatides; Preparation of compositions containing phosphatides of unknown structure
Definitions
- This invention relates to phosphatidic compositions, and more particularly to compositions resulting from treating 'phosphatides with alkali metal phosphates.
- phosphates of any of the alkali metals may be employed, the invention will be speclflcally described with respect to various sodium phosphates.
- the normal or trisodium phosphate produces a compound which is distinctly alkaline when combined with phosphatides. It has been proximately 10.5 even though excess alkali is separated from the compound. on the other hand. by employing a salt containing a lesser amount of alkali metal in the molecule such as metal. produce acid or at least neutral compounds with phosphatides.
- phosphates which have less than three alkali metal atoms for each phosphate group such as the acid phospha es line, for example, having a pH in the neighbor- 5.
- the original purified cornoilrphosphatide had a phosphorus content of approximately 2.1%, a nitrogen'content approximately 1.2% and a dispersed in water; whereas the resulting com and had a sodium content oi 5.7%, a phosphorus a nitrogen content of approximately 3%, pH oi approximately 7.
- Sodium hexametaphosphate also forms a compound with 'phosphatides which is substantially neutral.
- '25 gr. oi the corn phosphatide above referred to was mixed with 35 gr. of sodium hexametaphosphate in '70 gr. oi water, stirred for 3 hours at room temperature, and dehydrated at 65 C. for 18 hours in vacuo.
- This compound is unique in that, instead of an opaque pastelike mixture being iormed, the reaction mass is a clear, viscous oil very soluble in water.
- the oily material may be extracted with ether as described in the previous example in order to remove excess alkali or other unreacted products, and the resulting compound had a sodium content oi 5.8%, a phosphorus content of 6.2%, and produced a pH oi 7.1.
- the pH of the products oi either oi the above two examples may be made smaller by employing a mixture of monosodlum phosphate and disodlum phosphate in the first example and a mixture of monosodium phosphate and sodium hexametaphosphate in the second example.
- the acid and neutral compounds are extremely stable.
- the products oi the two examples above given may made more alkaline by employing mixtures of the disodium phosphate or sodium hexametaphosphate with trisodium phospha Other sodium be employed, for pyrophosphate either with any of the other phosphates herein mentioned to produce compositions having any desired pH.
- the products disperse in oil in the cold, and dissolve in oil when heated to, about 90 F., to give a clear solution which has a powerful emulsifying action toward water. They are soluble in ether and dispersable in water.
- the equivalent salts of potassium or other alkali metals may be employed instead of sodium salts to give similar results.
- Phosphatides other than the corn phosphatldes mentioned may likewise be employed to form the compounds oi the present invention.
- Corn phosp tides are preierred, as they are light, in color andcontain no linolenic acid radicals, thereby being more stable than such phosphatides assoya bean phosphatides.
- soya bean phosphatides are much darker in color and are likely to become still further colored if subjected to heat.
- Cottonseed phosphatides may also be employed, and produce compositions of high stability, but are usually quite highly colored.
- the corn phosphatldes are somewhat more acidic than soya bean phosphatldes. Thus; corn phosphatldes usually produce a pH between 4.5 and 4.8 when dispersed in water. while soya' bean phosphatides produce a pH in the neighborhood of 5.7. It has been iound that the corn phosphatides take up more and a content of 4.8%,
- the compounds or compositions of the present invention are useiul as emulsifying agents ior oil and water emulsions.
- All of the compounds mentioned are edible and can be employed in edible products. For example, they can be employed in the production of mayonnaise or margarine to retain water, emulsified with the oils or fats.
- Phosphatldes which are free or linolenic acid radicals such as corn and cottonseed phosphatldes are preferred ior use in edible products as they have no tendency to revert to an undesirable taste as is the case of soya bean phosphatidic compounds, which have a tendency to revert to the original flavor and odor oi the soya bean oil.
- compositions of the present invention with soya bean phosphatides are, however. more stable than the original soya bean ph'osphatides.
- the compounds of the present invention are particularly valuable in producing high ratio shortening (or baked products; that is to say, a small amount thereof, for example .25 to 5% and usually about 2% on the basis of the shortening, will enable ratios oi sugar to flour in excess oi one-to-one to be employed in cakes having increased volume and excellent texture.
- compositions oi the present invention are also useful as constituents in detergents, since they have excellent emulsifying properties and are compatible with all common detergent materials. They also have extremely good water softening properties, particularly compositions including substantial amounts oi the hexametaphosphate. They may be employed with alkali metal soaps to produce hard water soaps by preventing precipltation or decomposition of ina soluble alkali earth metal soaps such as those creams, nose drops,
- compositions oi calcium or. magnesium Smooth. stable emulsions oi vegetable, mineral or essential oils with water are obtained when small amounts, ior example .i to 5% oi the composition reierred to are added to either the water or oil phase and the resulting mixture thoroughly agitated.
- the compositions may also be blended with ingredients oi calves, olntments, face creams, shaving nose sprays, etc.. to produce smoother products having greater water retention properties. They are of value in insecticldal emulsions to prevent separation oi the components thereof and to cause said emulsions to spread when applied.
- the compositions oi the present invention merit dispersing agents ior oil paints and as emulsifiers in casein paints. Other uses oi the compositions are as emulsifiers in flotation processes, surface tension reducing agents in textile treatment, and wherever emulsifying or surface tension reducing agents are desired.
- an alkali metal stability and a pH when dispersed in water not substantially greater than 7.8 said compound resulting from reacting a phosphatide with an alkali metal phosphate having less than 3 atoms of alkali metal for each phosphate group.
- an alkali metal phosphate-phosphatidic composition having high stability and a pl-I when dispersed in water not substantially greater than 7.8, said compound phosphate-phosphatidic composition having high stabilityand a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with sodium hexametaphosphate.
- an alkali metal phpsphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially. greater than 7.8, said compound resulting from reacting a phosphatide which is free of linolenic acid radicals with a sodium phosphate having less than 3 atoms of alkali metal for each phosphate group.
- an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a corn phosphatide ,with a sodium phosphate having less than 3 atoms resulting from reacting a phosphatide with an l acid alkali metal phosphate.
- an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatlde with a mixture of alkali metal phosphates including a substantial quantity of an acid phosphate.
- an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with a mixture oi. alkali metal phosphates including asubstantial quantity of a monophosphate.
- an alkali metal phosphaterphostphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with a sodium phosphate having less than 3 atoms of alkali metal for each phosphate group.
- an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with disodium phosphate.
- the process of producing phosphatidic compounds containing alkali metals and having high stability which comprises, reacting a phosphatide in the presence of water with an alkali metal phosphate having lesfihan 3 alkali metal atoms for each phosphate group and dehydrat- .ing the resulting product.
- an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound re? sulting from reacting a phosph'atide with monoproduct.
- the process of producing sodiumphosphatephosphatidic compounds having high stability which comprises, reacting sodium hexametaphosphate in the presence of water with a phosphatide,
- the process of producing phosphatidic compoundscontaining alkali metals and having high stability comprises, reacting a phosphatide in the presence of water with a mixture oi alkali metal phosphates containing a substantial porticn of a monophosphate. and dehydrating said BENJAMIN H. THURMAN.
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Description
Patented Jan. 27, 1942 UNITED STATES PATEN T-OFFICE 2,271,409 PHOSPHATIDIC COMPOSITION Benjami H.
Thin-ma Bronxville, N. Y., assimito Beiiuin Inc., R eno, Nev., a corporation of vada No Drawing; Application December 29, 1939, Serial No. 311,705
16 Claims.
This invention relates to phosphatidic compositions, and more particularly to compositions resulting from treating 'phosphatides with alkali metal phosphates.
In my copending application Serial No. 290,083, filed August 14, 1939, of which this application is a continuation in phosphatides with various alkali metal salts, among which was a compound 01' sodium phosphate (NaaPOa) with phosphatides. When sumcient sodium phosphate is employed to react with substantially all of the phosphatldes, a resulting compound which is alkaline, that is, a compound which gives a pH substantially in excess of 7 when dissolved in water, is produced. In accordance with the present invention, I have found that alkali metal phosphate-phosphatide comor acidic properties.
Other objects and advantages oi the invention will appear in the following description or preierred embodiments thereof.
Although phosphates of any of the alkali metals may be employed, the invention will be speclflcally described with respect to various sodium phosphates. As stated above, the normal or trisodium phosphate produces a compound which is distinctly alkaline when combined with phosphatides. It has been proximately 10.5 even though excess alkali is separated from the compound. on the other hand. by employing a salt containing a lesser amount of alkali metal in the molecule such as metal. produce acid or at least neutral compounds with phosphatides. Also. phosphates which have less than three alkali metal atoms for each phosphate group such as the acid phospha es line, for example, having a pH in the neighbor- 5. are quite unstable and will even split into the phosphate and phosphatide it alvacuo for 2% hours at to water in the dehydrated mass had been reduced or such salts as the meta pH oi approximately 4.6 when to approximately 1%, a pasty material remained. The paste was extracted with petroleum ether and the ether extract subjected to vacuum treatment to remove the ether. The resulting product was a clear, amber, which was odorless and had a slightly-salty taste.
The original purified cornoilrphosphatide had a phosphorus content of approximately 2.1%, a nitrogen'content approximately 1.2% and a dispersed in water; whereas the resulting com and had a sodium content oi 5.7%, a phosphorus a nitrogen content of approximately 3%, pH oi approximately 7.
Sodium hexametaphosphate also forms a compound with 'phosphatides which is substantially neutral. As a specific example of making such a compound, '25 gr. oi the corn phosphatide above referred to was mixed with 35 gr. of sodium hexametaphosphate in '70 gr. oi water, stirred for 3 hours at room temperature, and dehydrated at 65 C. for 18 hours in vacuo. This compound is unique in that, instead of an opaque pastelike mixture being iormed, the reaction mass is a clear, viscous oil very soluble in water. I! desired, the oily material may be extracted with ether as described in the previous example in order to remove excess alkali or other unreacted products, and the resulting compound had a sodium content oi 5.8%, a phosphorus content of 6.2%, and produced a pH oi 7.1.
The pH of the products oi either oi the above two examples may be made smaller by employing a mixture of monosodlum phosphate and disodlum phosphate in the first example and a mixture of monosodium phosphate and sodium hexametaphosphate in the second example. As stated above, the acid and neutral compounds are extremely stable. However, ii desired, the products oi the two examples above given may made more alkaline by employing mixtures of the disodium phosphate or sodium hexametaphosphate with trisodium phospha Other sodium be employed, for pyrophosphate either with any of the other phosphates herein mentioned to produce compositions having any desired pH. The products disperse in oil in the cold, and dissolve in oil when heated to, about 90 F., to give a clear solution which has a powerful emulsifying action toward water. They are soluble in ether and dispersable in water. The equivalent salts of potassium or other alkali metals may be employed instead of sodium salts to give similar results.
Phosphatides other than the corn phosphatldes mentioned may likewise be employed to form the compounds oi the present invention. Corn phosp tides are preierred, as they are light, in color andcontain no linolenic acid radicals, thereby being more stable than such phosphatides assoya bean phosphatides. Furthermore, the soya bean phosphatides are much darker in color and are likely to become still further colored if subjected to heat. Cottonseed phosphatides may also be employed, and produce compositions of high stability, but are usually quite highly colored. The corn phosphatldes are somewhat more acidic than soya bean phosphatldes. Thus; corn phosphatldes usually produce a pH between 4.5 and 4.8 when dispersed in water. while soya' bean phosphatides produce a pH in the neighborhood of 5.7. It has been iound that the corn phosphatides take up more and a content of 4.8%,
. tion, as the chemistry is sodium and phosphorus than those irom scya bean phosphatides. It is believed that the reaction between the sodium phosphate employed and the phosphatide is an acid-base combination and that the more acidic material (corn phosphatides) reacts with larger amounts oi the basic material, although applicant does not wish to be bound by any precise theory oi combinaextremely complex.
The compounds or compositions of the present invention, particularly those having acid characteristics and greater stability, are useiul as emulsifying agents ior oil and water emulsions. All of the compounds mentioned are edible and can be employed in edible products. For example, they can be employed in the production of mayonnaise or margarine to retain water, emulsified with the oils or fats. Phosphatldes which are free or linolenic acid radicals such as corn and cottonseed phosphatldes are preferred ior use in edible products as they have no tendency to revert to an undesirable taste as is the case of soya bean phosphatidic compounds, which have a tendency to revert to the original flavor and odor oi the soya bean oil. The compositions of the present invention with soya bean phosphatides are, however. more stable than the original soya bean ph'osphatides. The compounds of the present invention are particularly valuable in producing high ratio shortening (or baked products; that is to say, a small amount thereof, for example .25 to 5% and usually about 2% on the basis of the shortening, will enable ratios oi sugar to flour in excess oi one-to-one to be employed in cakes having increased volume and excellent texture.
The compositions oi the present invention are also useful as constituents in detergents, since they have excellent emulsifying properties and are compatible with all common detergent materials. They also have extremely good water softening properties, particularly compositions including substantial amounts oi the hexametaphosphate. They may be employed with alkali metal soaps to produce hard water soaps by preventing precipltation or decomposition of ina soluble alkali earth metal soaps such as those creams, nose drops,
oi calcium or. magnesium. Smooth. stable emulsions oi vegetable, mineral or essential oils with water are obtained when small amounts, ior example .i to 5% oi the composition reierred to are added to either the water or oil phase and the resulting mixture thoroughly agitated. The compositions may also be blended with ingredients oi calves, olntments, face creams, shaving nose sprays, etc.. to produce smoother products having greater water retention properties. They are of value in insecticldal emulsions to prevent separation oi the components thereof and to cause said emulsions to spread when applied. The compositions oi the present invention merit dispersing agents ior oil paints and as emulsifiers in casein paints. Other uses oi the compositions are as emulsifiers in flotation processes, surface tension reducing agents in textile treatment, and wherever emulsifying or surface tension reducing agents are desired.
while, for the want oi a better term, I have herein referred to my new chemical compounds as "phosphatidic compounds," it is nevertheless to be understood that the ly dissimilar in composition, behavior and utility to the usual soy bean lecithin oi commerce.
While I have disclosed the preferred embodialso' have utility aapigsame are iundamentalsodium phosphate. 7
9. As a product of manufacture, an alkali metal stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with an alkali metal phosphate having less than 3 atoms of alkali metal for each phosphate group.
3. As a product of manufacture, an alkali metal phosphate-phosphatidic composition having high stability and a pl-I when dispersed in water not substantially greater than 7.8, said compound phosphate-phosphatidic composition having high stabilityand a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with sodium hexametaphosphate.
10. As a product of manufacture, an alkali metal phpsphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially. greater than 7.8, said compound resulting from reacting a phosphatide which is free of linolenic acid radicals with a sodium phosphate having less than 3 atoms of alkali metal for each phosphate group.
11. As a product of manufacture, an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a corn phosphatide ,with a sodium phosphate having less than 3 atoms resulting from reacting a phosphatide with an l acid alkali metal phosphate.
4. As a product of manufacture, an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatlde with a mixture of alkali metal phosphates including a substantial quantity of an acid phosphate.
5. As a product of manufacture, an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with a mixture oi. alkali metal phosphates including asubstantial quantity of a monophosphate.
6. As a product of manufacture, an alkali metal phosphaterphostphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with a sodium phosphate having less than 3 atoms of alkali metal for each phosphate group.
'I. As a product of manufacture, an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound resulting from reacting a phosphatide with disodium phosphate.
of alkali metal for each phosphate, group.
12. The process of producing phosphatidic compounds containing alkali metals and having high stability, which comprises, reacting a phosphatide in the presence of water with an alkali metal phosphate having lesfihan 3 alkali metal atoms for each phosphate group and dehydrat- .ing the resulting product.
3. As a product of manufacture, an alkali metal phosphate-phosphatidic composition having high stability and a pH when dispersed in water not substantially greater than 7.8, said compound re? sulting from reacting a phosph'atide with monoproduct.
sodium ato'ms for each phosphate group, dehydrating the resulting reaction products, extracting said compound i'rom.said reaction products with a solvent for said compound, and evaporating said solvent from said compound.
15. The process of producing sodiumphosphatephosphatidic compounds having high stability, which comprises, reacting sodium hexametaphosphate in the presence of water with a phosphatide,
and dehydrating the resulting product.
l6. The process of producing phosphatidic compoundscontaining alkali metals and having high stabilitywhich' comprises, reacting a phosphatide in the presence of water with a mixture oi alkali metal phosphates containing a substantial porticn of a monophosphate. and dehydrating said BENJAMIN H. THURMAN.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US311705A US2271409A (en) | 1939-12-29 | 1939-12-29 | Phosphatidic composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US311705A US2271409A (en) | 1939-12-29 | 1939-12-29 | Phosphatidic composition |
Publications (1)
Publication Number | Publication Date |
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US2271409A true US2271409A (en) | 1942-01-27 |
Family
ID=23208090
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US311705A Expired - Lifetime US2271409A (en) | 1939-12-29 | 1939-12-29 | Phosphatidic composition |
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US (1) | US2271409A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2444984A (en) * | 1943-07-21 | 1948-07-13 | W J Fitzpatrick Company | Stabilized lecithin |
US2545186A (en) * | 1947-06-02 | 1951-03-13 | Shell Dev | Nonaqueous insecticidal emulsions containing organic esters of phosphorous acids |
US2589326A (en) * | 1949-12-21 | 1952-03-18 | Socony Vacuum Oil Co Inc | Organic phosphorus ester-p2s5 reaction products and oil compositions containing the same |
US2997398A (en) * | 1958-07-14 | 1961-08-22 | American Lecithin Co | Coating compositions |
WO2014056563A1 (en) | 2012-10-09 | 2014-04-17 | Clariant International Ltd | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
-
1939
- 1939-12-29 US US311705A patent/US2271409A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2444984A (en) * | 1943-07-21 | 1948-07-13 | W J Fitzpatrick Company | Stabilized lecithin |
US2545186A (en) * | 1947-06-02 | 1951-03-13 | Shell Dev | Nonaqueous insecticidal emulsions containing organic esters of phosphorous acids |
US2589326A (en) * | 1949-12-21 | 1952-03-18 | Socony Vacuum Oil Co Inc | Organic phosphorus ester-p2s5 reaction products and oil compositions containing the same |
US2997398A (en) * | 1958-07-14 | 1961-08-22 | American Lecithin Co | Coating compositions |
WO2014056563A1 (en) | 2012-10-09 | 2014-04-17 | Clariant International Ltd | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
US9303143B2 (en) * | 2012-10-09 | 2016-04-05 | Clariant International Ltd. | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
US9303144B2 (en) * | 2012-10-09 | 2016-04-05 | Clariant International Ltd. | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
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