US2553441A - Stabilization of organic materials - Google Patents

Stabilization of organic materials Download PDF

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US2553441A
US2553441A US738210A US73821047A US2553441A US 2553441 A US2553441 A US 2553441A US 738210 A US738210 A US 738210A US 73821047 A US73821047 A US 73821047A US 2553441 A US2553441 A US 2553441A
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inhibitor
hydroquinone
oil
oils
aminomethyl
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Joseph A Chenicek
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Universal Oil Products Co
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/223—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond having at least one amino group bound to an aromatic carbon atom
    • C10L1/2235—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond having at least one amino group bound to an aromatic carbon atom hydroxy containing
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/17—Amines; Quaternary ammonium compounds
    • C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B5/00—Preserving by using additives, e.g. anti-oxidants
    • C11B5/0021—Preserving by using additives, e.g. anti-oxidants containing oxygen
    • C11B5/0035—Phenols; Their halogenated and aminated derivates, their salts, their esters with carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/221—Six-membered rings containing nitrogen and carbon only
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226—Morpholines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/30—Heterocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10—Semi-solids; greasy

Definitions

  • This invention relates to the stabilization of organic compounds which tend to deteriorate in storage or in use due to oxidation reactions.
  • the invention is particularly applicable to the stabilization of edible fats and oils which generally are of animal or vegetable origin and which tend to become rancid, especially during long periods of storage prior to use.
  • Typical representatives of these edible fats and oils include linseed oil, menhaden oil, cod liver oil, castor oil,
  • R is hydrogen, alkyl, aralkyl, aryl or alkaryl radical
  • R' is a disubstituted aminomethyl radical
  • oils and fats such as are sold under various trade names including Spry, Crisco, Snowdrift,
  • oils and fats may be-treated within the scope of the present invention, including oils and fats which have previously been subjected to various treatments, such as blowing with air, heat treatment, 'etc.
  • the present invention relates to a method of stabilizing an organic material subject to oxidative deterioration which comprises-adding thereto an inhibitor comprising a disubstituted aminomethyl dihydroxybenzene.
  • inhibitors of the present invention may be Where R and R are alkyl or substituted alkyl radicals and R is hydrogen, suitable compounds include 2-dimethylaminomethyl-hydroquinone,
  • R" is an alkyl or substituted alkyl radical
  • R" is an alkyl or substituted alkyl radical
  • R" is an alkyl or substituted alkyl radical
  • methoxyphenol, etc. of a hydroquinone or 4-alkoxyphenol type include those in which R and R are cycloalkyl radicals as illustrated by 2-dicyclohexylaminomethylhydroquinone and 2-dicyclohexylaminomethyl-4 alkoxyphenols.
  • the alkoxy group may 1 comprise ethoxy, methoxy, propoxy, butoxy, penti oXy, etc. radicals.
  • Another class of compounds within the scope '.of the present invention include those in which 2-dimethyland ethylcyclohexylaminm R and R. are carbon atoms of a heterocyclic ring.
  • Heterocyclic rings include those derived from morpholine, piperazine, piperidine, and pyrrolidine.
  • R comprises a disubstituted-aminomethyl radical
  • Suitable compounds include 2,5-bis-(dimethylaminomethyl) hydroquinone, 2,5-bis-(morpholinomethyl)-4-hydroxyphenol, etc. and particularly 2,5 bis (diethylaminomethyl) -hydroquinone.
  • the various compounds which may be prepared and used within the broad scope of the present invention are not necessarily equivalent in their activity.
  • the total number of carbon atoms in the inhibitor isnot greater than about 25, as it has been found that, within certain limits, the potency of the inhibitor decreases with inclusion of hydrocarbon radicals of high molecular weight.
  • the inhibitors of the present invention may be prepared in any suitable manner.
  • a particularly satisfactory method is to react the desired dialkylamine, formaldehyde, and either hydroquinone or the desired 4-alkoxyphenol under refluxing conditions for a time sufficient to complete the reaction.
  • the products are separated and recovered by conventional methods. Specific details as to the preparation of these compounds are shown in the examples hereinafter set forth.
  • the inhibitor of the present invention is generally added to the organic material in amounts of less. than 1% by weight and preferably within the range of from about 0.001% to about 0.5% by weight.
  • the inhibitor may be used alone or in conjunction with synergists, inhibitor activators, dyes, antiknock agents, etc., depending upon the material to be treated.
  • a synergist such as phosphoric acid, ascorbic acid, etc.
  • a dye and perhaps an inhibitor activator such as certainv types of alkylene polyamines, may be used.
  • Example 1 2,5! bis (diethylaminomethyl) -hydroquinone was prepared as follows: hydroquinone and diethylamine were placed in a 3-necked flask fitted with a stirrer, thermometer and droppingfunnel. A 35% formaldehyde-aqueous solution was added dropwise to the mixture which was stirred and maintained at a temperature of 2030 C. The reaction product was extracted with ether, dried, the ether evaporated, and the residue recrystallized from methyl alcohol.
  • the 2,5-bis- (diethylaminomethyl) -hydroquinone prepared in the above manner was used to stabilize lard.
  • the lard had a normal stability period of 1 hours as determined by the Swift test. This test is described in detail in the article by A. E. King, H. L. Roschen and W. H. Irwin, which appeared in the Oil and Soap vol. X, No. 6, pages 105 to 109 1933). In general, this test comprises bubbling air through a sample of the lard until rancidity is determined organoleptically and by peroxide. Values.
  • Example 2 2-dimethyl aminomethyl 4 methoxyphenol was prepared in substantially the same manner as the inhibitor of Example 1 except that 4- methoxyphenol was used instead of hydroquinone and dimethylamine was used in place of diethylamine. This inhibitor was used to stabilize another sample of the same lard. 0.02% by weight of this inhibitor increased the stability period of the lard to reach a peroxide number of 20 from 1 /4 hours to 35 hours.
  • Example 3 2 morpholinomethyl-4-methoxyphenol, likewise prepared in a similar manner, was also tested in another sample of the same lard. This inhibitor increased the stability period of the lard from 1 hours to 22 hours.
  • Example 4 2-dimethylaminomethyl-4-methoxyphenol wasv used to stabilize Pennsylvania cracked gasoline which had a blank induction period of 105 minutes. Upon the addition of 0.05% by weight of this inhibitor, the induction period of the cracked gasoline was increased from 105 minutes to 435 minutes. The induction period is deter mined by the Oxygen Bomb Stability Test which is a. standard method for evaluating the storage stability of gasoline.
  • Example 5 0.05% by weight of 2,5-bis-(morpholinomethyl) -hydroquinone increased the induction period of another sample of the Pennsylvania cracked gasoline used in Example 4 from 105 prises adding thereto an inhibitor comprising a 2,5 -bis- (dialkylamino-methyl) -hydroquino-ne.
  • a method of stabilizing edible fats and oils against rancidity which comprises incorporating therein from about 0.005% to about 0.1% of an inhibitor comprising a 2,5-bis-(dialkylaminomethyl) -hydroquinone.
  • a method of stabilizing edible fats and oils against rancidity which comprises incorporating against rancidity which comprises incorporating therein from about 0.005%. to about 0.1% of an inhibitor comprising 2-dimethy1aminomethyl-4- methoxyphenol.
  • a method of stabilizing edible fats and oils against rancidity which comprises incorporating therein from about 0.005% to about 0.1% of an inhibitor comprising 2 morpholinomethyl 4- methoxyphenol.
  • An organic compound tending to deteriorate due to oxygen containing a disubstitutedaminomethyl-dihydroxybenzene in an amount sufiicient to retard said oxidative deterioration.
  • Edible fats and oils tending to become rancid containing a 2,5-bis-(dialkylaminomethyl)- hydroquinone in an amount sufiicient to retard rancidity.
  • Edible fats and oils tending to become rancid containing 2,5-bis-(diethylaminomethyl) -hydroquinone in an amount sufiicient to retard rancidity.
  • a method of stabilizing an organic material subject to oxidative deterioration which comprises adding thereto an inhibitor selected from the group consisting of a disubstituted aminomethyl-dihydroxybenzene and a dialkylaminomethyl-i-alkoxyphenol.
  • a method of stabilizing edible fats and oils 'alkoxyphenol in an amount sufficient to retard rancidity 14.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Emergency Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Fats And Perfumes (AREA)

Description

Patented May 1951 STABILIZATION oF ORGANIC MATERIALS Joseph A. Chenicek, Riverside, Ill., assignor to Universal ,Oil Products Company, Chicago, Ill., a corporation of Delaware:
No Drawing. Application March 29, 1947, Serial No. 738,210
16 Claims.
This invention relates to the stabilization of organic compounds which tend to deteriorate in storage or in use due to oxidation reactions.
Various organic compounds including motor fuel and particularly cracked gasoline and polymer gasoline, mineral oil, lubricating oil, fuel oil, drying oil, greases, rubber, edible fats and oils, etc, are adversely affected by oxygen, with the resultant formation of undesirable gum, discoloration, rancidity, or other deleterious reactions.
The invention is particularly applicable to the stabilization of edible fats and oils which generally are of animal or vegetable origin and which tend to become rancid, especially during long periods of storage prior to use. Typical representatives of these edible fats and oils include linseed oil, menhaden oil, cod liver oil, castor oil,
are carbon atoms of a heterocyclic ring,'R" is hydrogen, alkyl, aralkyl, aryl or alkaryl radical,
and R' is a disubstituted aminomethyl radical,
' hydrogen, alkyl, aralkyl, aryl or alkaryl radical.
olive oil, rapeseedoil, coconut oil, palm oil, corn oil, sesame oil, peanut oil, babassu oil, butter, fat, lard, beef tallow,-etc., as well as hydrogenated oils and fats such as are sold under various trade names including Spry, Crisco, Snowdrift,
etc. 7 It is understood that other oils and fats may be-treated within the scope of the present invention, including oils and fats which have previously been subjected to various treatments, such as blowing with air, heat treatment, 'etc.
i In one embodiment the present invention relates to a method of stabilizing an organic material subject to oxidative deterioration which comprises-adding thereto an inhibitor comprising a disubstituted aminomethyl dihydroxybenzene.
In a specific embodiment the present invention relates to a method of stabilizing edible fats and oils against rancidity which comprises incorporating therein a dialkylaminomethyl-dihydroxy- In another specific embodiment the present invention relates to a method of stabilizing edible fats and oils against rancidity which comprises incorporating therein an inhibitor comprising a:
2,5-bis- (dialkylaminomethyl) -hydroquino-ne.
The inhibitors of the present invention may be Where R and R are alkyl or substituted alkyl radicals and R is hydrogen, suitable compounds include 2-dimethylaminomethyl-hydroquinone,
2-diethylaminomethyl-hydroquinone, Z-dipropylaminomethyl-hydroquinone, Z-dibutylaminomethyl-hydroquinone, 2-diamylaminomethylhydroquinone, 2-di-,8-hydroxyethylaminomethylhydroquinone. Derivatives in which R" is an alkyl or substituted alkyl radical include such compounds as 2dimethylaminomethyl-4-rneth- 2-diethylaminomethyl-4-methoxy-- 2-dipropylaminomethyl-4-methoXypheoxyphenol, phenol, nol, 2-diamylaminomethyl-4-methoxyphenol, 2- dimethylaminomethyl-4ethoxyphenol, Z-diethyl aminomethy1-4-ethoxyphenol, 2 -dipropylaminomethyl-l-ethoxyphenol, Z-dibutylairfinomethyl- 4-ethoxyphenol, 2-diamylaminomethyl-4-ethoxyphenol, 2-dimethylaminomethyl-4-propoxyphenol, 2-diethylaminomethyl-4-propoxyphenol, 2-' dipropylaminomethyl-4-propoxyphenol,
2-dibutylaminornethyl-4-propoxyphenol,
aminomethyl-4-butoxyphenol, Z-diethylaminomethyl-i-butoxyphenol, 2-dipropylaminomethylw Z-dibutylaminomethyl 4 bu-' toxyphenol. 2-di-,9-hydroxyethylaminomethyll- Other suitable compounds 4-butoxyphenol,
methoxyphenol, etc. of a hydroquinone or 4-alkoxyphenol type include those in which R and R are cycloalkyl radicals as illustrated by 2-dicyclohexylaminomethylhydroquinone and 2-dicyclohexylaminomethyl-4 alkoxyphenols. Here again the alkoxy group may 1 comprise ethoxy, methoxy, propoxy, butoxy, penti oXy, etc. radicals.
different. I
such as nethylethylaminomethyl, methylpropylaminomethyl, methylbutyl-aminomethyl, methylamyl-aminomethyl, ethylpropyl-aminomethyl,
ethylbutyl-aminomethyl, ethylamyl-aminomethyl propylbutyl-aminomethyl, propylamyl-aminomethyl, butylamyl-am'inomethyl, etc. and radicals "in which R- is an alkyl group and R is a cycloalkyl group as in suchradicals as methylcyclohexylaminomethyl methyl. v
Another class of compounds within the scope '.of the present invention include those in which 2-dimethyland ethylcyclohexylaminm R and R. are carbon atoms of a heterocyclic ring. Heterocyclic rings include those derived from morpholine, piperazine, piperidine, and pyrrolidine.
Referring again to the structural formula heretofore set forth when R comprises a disubstituted-aminomethyl radical, it generally will be the same as the group attached in the 2-position. Suitable compounds include 2,5-bis-(dimethylaminomethyl) hydroquinone, 2,5-bis-(morpholinomethyl)-4-hydroxyphenol, etc. and particularly 2,5 bis (diethylaminomethyl) -hydroquinone.
It is understood that the various compounds which may be prepared and used within the broad scope of the present invention are not necessarily equivalent in their activity. In general it is preferred that the total number of carbon atoms in the inhibitor isnot greater than about 25, as it has been found that, within certain limits, the potency of the inhibitor decreases with inclusion of hydrocarbon radicals of high molecular weight.
The inhibitors of the present invention may be prepared in any suitable manner. A particularly satisfactory method is to react the desired dialkylamine, formaldehyde, and either hydroquinone or the desired 4-alkoxyphenol under refluxing conditions for a time sufficient to complete the reaction. The products are separated and recovered by conventional methods. Specific details as to the preparation of these compounds are shown in the examples hereinafter set forth.
The inhibitor of the present invention is generally added to the organic material in amounts of less. than 1% by weight and preferably within the range of from about 0.001% to about 0.5% by weight. The inhibitor may be used alone or in conjunction with synergists, inhibitor activators, dyes, antiknock agents, etc., depending upon the material to be treated. For example, when used in edible fats and oils, a synergist such as phosphoric acid, ascorbic acid, etc., will generally be added along with the inhibitor. When used in gasoline, lead tetraethyl, a dye and perhaps an inhibitor activator, such as certainv types of alkylene polyamines, may be used.
The following examples are introduced to illustrate further the novelty and utility of the present invention, but not with the intention of unduly limiting the same.
Example 1 2,5! bis (diethylaminomethyl) -hydroquinone was prepared as follows: hydroquinone and diethylamine were placed in a 3-necked flask fitted with a stirrer, thermometer and droppingfunnel. A 35% formaldehyde-aqueous solution was added dropwise to the mixture which was stirred and maintained at a temperature of 2030 C. The reaction product was extracted with ether, dried, the ether evaporated, and the residue recrystallized from methyl alcohol.
The 2,5-bis- (diethylaminomethyl) -hydroquinone prepared in the above manner was used to stabilize lard. The lard had a normal stability period of 1 hours as determined by the Swift test. This test is described in detail in the article by A. E. King, H. L. Roschen and W. H. Irwin, which appeared in the Oil and Soap vol. X, No. 6, pages 105 to 109 1933). In general, this test comprises bubbling air through a sample of the lard until rancidity is determined organoleptically and by peroxide. Values.
0.02% by weight of the above inhibitor in- 4 creased the number of hours until the lard developed a peroxide number of 20 from 1% hours to 72 hours.
Example 2 2-dimethyl aminomethyl 4 methoxyphenol was prepared in substantially the same manner as the inhibitor of Example 1 except that 4- methoxyphenol was used instead of hydroquinone and dimethylamine was used in place of diethylamine. This inhibitor was used to stabilize another sample of the same lard. 0.02% by weight of this inhibitor increased the stability period of the lard to reach a peroxide number of 20 from 1 /4 hours to 35 hours.
Example 3 2 morpholinomethyl-4-methoxyphenol, likewise prepared in a similar manner, was also tested in another sample of the same lard. This inhibitor increased the stability period of the lard from 1 hours to 22 hours.
Example 4 2-dimethylaminomethyl-4-methoxyphenol wasv used to stabilize Pennsylvania cracked gasoline which had a blank induction period of 105 minutes. Upon the addition of 0.05% by weight of this inhibitor, the induction period of the cracked gasoline was increased from 105 minutes to 435 minutes. The induction period is deter mined by the Oxygen Bomb Stability Test which is a. standard method for evaluating the storage stability of gasoline.
Example 5 0.05% by weight of 2,5-bis-(morpholinomethyl) -hydroquinone increased the induction period of another sample of the Pennsylvania cracked gasoline used in Example 4 from 105 prises adding thereto an inhibitor comprising a 2,5 -bis- (dialkylamino-methyl) -hydroquino-ne.
5-. A method of stabilizing edible fats and oils against rancidity which comprises incorporating therein from about 0.005% to about 0.1% of an inhibitor comprising a 2,5-bis-(dialkylaminomethyl) -hydroquinone.
6. A method of stabilizing edible fats and oils against rancidity which comprises incorporating against rancidity which comprises incorporating therein from about 0.005%. to about 0.1% of an inhibitor comprising 2-dimethy1aminomethyl-4- methoxyphenol.
9. A method of stabilizing edible fats and oils against rancidity which comprises incorporating therein from about 0.005% to about 0.1% of an inhibitor comprising 2 morpholinomethyl 4- methoxyphenol.
10. An organic compound tending to deteriorate due to oxygen containing a disubstitutedaminomethyl-dihydroxybenzene in an amount sufiicient to retard said oxidative deterioration.
11. Edible fats and oils tending to become rancid containing a 2,5-bis-(dialkylaminomethyl)- hydroquinone in an amount sufiicient to retard rancidity.
12. Edible fats and oils tending to become rancid containing 2,5-bis-(diethylaminomethyl) -hydroquinone in an amount sufiicient to retard rancidity.
13. A method of stabilizing an organic material subject to oxidative deterioration which comprises adding thereto an inhibitor selected from the group consisting of a disubstituted aminomethyl-dihydroxybenzene and a dialkylaminomethyl-i-alkoxyphenol.
14. A method of stabilizing edible fats and oils 'alkoxyphenol in an amount sufficient to retard rancidity.
JOSEPH A. CHENICEK.
REFERENCES CITED The following references are of record in the 20 file of this patent:
therein from about 0.005% to about 0.1% of an UNITED STATES PATENTS Number Name Date 1,745,604 Christiansen et a1. Feb. 4, 1930 2,050,689 Briod Aug. 11, 1936 2,050,732 Roberts Aug. 11, 1936 2,233,172 Loane Feb. 25, 1941

Claims (1)

1. A METHOD OF STABILIZING AN ORGANIC MATERIAL SUBJECT TO OXIDATIVE DETERIORATION WHICH COMPRISES ADDING THERETO AN INHIBITOR COMPRISING A DISUBSTITUTED AMINOMETHYL-DIHYDROXYBENZENE.
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Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2684293A (en) * 1952-01-22 1954-07-20 Ethyl Corp Stabilized tetraethyllead compositions
US2686124A (en) * 1951-11-15 1954-08-10 Us Agriculture Stabilization of forage crops with hydroquinone derivatives
US2686724A (en) * 1949-08-12 1954-08-17 Universal Oil Prod Co Stabilization of edible fats and oils
US2763616A (en) * 1952-05-24 1956-09-18 Socony Mobil Oil Co Inc Alkylthiohydroquinones-formaldehyde-amine reaction products and petroleum fractions, containing the same
US2796336A (en) * 1953-03-23 1957-06-18 Ethyl Corp Synergistic antioxidant composition and use
US2833634A (en) * 1953-01-26 1958-05-06 Ethyl Corp Synergistic antioxidants and their use
US3496172A (en) * 1968-09-16 1970-02-17 Merck & Co Inc Process for the preparation of alpha-lower acylamino - alpha - methyl - beta - (substituted phenyl) propionitriles
US3770397A (en) * 1972-06-19 1973-11-06 Mobil Oil Corp Liquid hydrocarbon fuels containing alkali metal salts of alkyl and dialkyl-aminoalkyl phenols, as antiknock agents
US4322304A (en) * 1980-04-29 1982-03-30 Phillips Petroleum Company Bis(disubstituted aminomethyl)phenols as ashless hydrocarbon additives
US4378231A (en) * 1980-10-24 1983-03-29 Phillips Petroleum Company Motor fuel
WO1984000545A1 (en) * 1982-07-26 1984-02-16 American Hospital Supply Corp Aryl substituted aminomethyl benzene derivatives useful as antiarrhythmic agents
EP0267715A1 (en) * 1986-10-31 1988-05-18 Betz Europe, Inc. Compositions comprising alkoxylated mannich products and their use
US4847415A (en) * 1988-06-01 1989-07-11 Betz Laboratories, Inc. Methods and composition for deactivating iron in hydrocarbon fluids
US4883580A (en) * 1988-06-01 1989-11-28 Betz Laboratories, Inc. Methods for deactivating iron in hydrocarbon fluids
US4888283A (en) * 1985-04-01 1989-12-19 Consiglio Nazionale Delle Ricerche Selective inhibitors of benzylaminoxidases with respect to other aminoxidases
US4894139A (en) * 1986-09-05 1990-01-16 Betz Laboratories, Inc. Methods for deactivating copper in hydrocarbon fluids

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1745604A (en) * 1927-11-05 1930-02-04 Squibb & Sons Inc Preservation of oils
US2050689A (en) * 1931-12-31 1936-08-11 Nat Oil Prod Co Process for controlling the oxidation of certain organic compounds and the products produced thereby
US2050732A (en) * 1933-11-13 1936-08-11 Standard Oil Co Process for storing motor fuels
US2233172A (en) * 1936-12-16 1941-02-25 Standard Oil Co Coated paper

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1745604A (en) * 1927-11-05 1930-02-04 Squibb & Sons Inc Preservation of oils
US2050689A (en) * 1931-12-31 1936-08-11 Nat Oil Prod Co Process for controlling the oxidation of certain organic compounds and the products produced thereby
US2050732A (en) * 1933-11-13 1936-08-11 Standard Oil Co Process for storing motor fuels
US2233172A (en) * 1936-12-16 1941-02-25 Standard Oil Co Coated paper

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2686724A (en) * 1949-08-12 1954-08-17 Universal Oil Prod Co Stabilization of edible fats and oils
US2686124A (en) * 1951-11-15 1954-08-10 Us Agriculture Stabilization of forage crops with hydroquinone derivatives
US2684293A (en) * 1952-01-22 1954-07-20 Ethyl Corp Stabilized tetraethyllead compositions
US2763616A (en) * 1952-05-24 1956-09-18 Socony Mobil Oil Co Inc Alkylthiohydroquinones-formaldehyde-amine reaction products and petroleum fractions, containing the same
US2833634A (en) * 1953-01-26 1958-05-06 Ethyl Corp Synergistic antioxidants and their use
US2796336A (en) * 1953-03-23 1957-06-18 Ethyl Corp Synergistic antioxidant composition and use
US3496172A (en) * 1968-09-16 1970-02-17 Merck & Co Inc Process for the preparation of alpha-lower acylamino - alpha - methyl - beta - (substituted phenyl) propionitriles
US3770397A (en) * 1972-06-19 1973-11-06 Mobil Oil Corp Liquid hydrocarbon fuels containing alkali metal salts of alkyl and dialkyl-aminoalkyl phenols, as antiknock agents
US4322304A (en) * 1980-04-29 1982-03-30 Phillips Petroleum Company Bis(disubstituted aminomethyl)phenols as ashless hydrocarbon additives
US4378231A (en) * 1980-10-24 1983-03-29 Phillips Petroleum Company Motor fuel
WO1984000545A1 (en) * 1982-07-26 1984-02-16 American Hospital Supply Corp Aryl substituted aminomethyl benzene derivatives useful as antiarrhythmic agents
US4888283A (en) * 1985-04-01 1989-12-19 Consiglio Nazionale Delle Ricerche Selective inhibitors of benzylaminoxidases with respect to other aminoxidases
US4894139A (en) * 1986-09-05 1990-01-16 Betz Laboratories, Inc. Methods for deactivating copper in hydrocarbon fluids
EP0267715A1 (en) * 1986-10-31 1988-05-18 Betz Europe, Inc. Compositions comprising alkoxylated mannich products and their use
US4810354A (en) * 1986-10-31 1989-03-07 Betz Laboratories, Inc. Bifunctional antifoulant compositions and methods
US4847415A (en) * 1988-06-01 1989-07-11 Betz Laboratories, Inc. Methods and composition for deactivating iron in hydrocarbon fluids
US4883580A (en) * 1988-06-01 1989-11-28 Betz Laboratories, Inc. Methods for deactivating iron in hydrocarbon fluids

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