US2153143A - Nondiscoloring, liquid antiseptic soap - Google Patents
Nondiscoloring, liquid antiseptic soap Download PDFInfo
- Publication number
- US2153143A US2153143A US187557A US18755738A US2153143A US 2153143 A US2153143 A US 2153143A US 187557 A US187557 A US 187557A US 18755738 A US18755738 A US 18755738A US 2153143 A US2153143 A US 2153143A
- Authority
- US
- United States
- Prior art keywords
- oil
- soap
- hardwood
- liquid
- antiseptic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/08—Liquid soap, e.g. for dispensers; capsuled
-
- 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
- C11D9/045—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps containing substances which prevent the deterioration of soaps, e.g. light or heat stabilisers or antioxidants
-
- 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
- C11D9/06—Inorganic compounds
- C11D9/08—Water-soluble compounds
- C11D9/10—Salts
-
- 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
Definitions
- the hardwood oil is purified either 5 b y distillation, only a fraction boiling between 180 C. and 240 C. being used, or by alkali treatgg ggiggggg g ggsgz a g soap ment, only the caustic-soluble portion of the oil Essential Oils 1 being used.
- Other substances such, for instance, Ethy1a1coh1"" u 5 15 as pine tar oil and/or essential oils, may al Water be incorporated in the liquid soap.
- the hardwoodoil may suitably amount to from 0.5% to It will be understood that the proportions are 33%, by l of th liquid antiseptic soa,p by way of illustration only.
- the blending 20 We prefer to use from 5% to 15% of the harde s which We may use, e ay e t o o 20 wood oil. example, in addition to ethyl alcohol: methanol,
- One object of our invention is to provide a hyle'ne lycol, di thy ly l, ethylene ly liquid, antiseptic soap containing hardwood oil, monomethyl o e ylene glycol monoethyl 30 which will not darken in the li ht a d i Qther ether,
- pr magnesium is add d to a, liquid, antiseptic p erably 0.25 gram, of an iodide or bromide of containing a hardwood oil, darkening of the oil, Potassium, Sodium. a t barium. and consequently of the soap, on contact with Strontium calcium or magnesium P 100 light and air is prevented, We have found such amounts to be very eil'ective. 40
- the heavy oils and tars which settle out of p nil 7,5 the raw pyroligneous acid resulting from the s ti l oils 3,0 destructive distillation-of hardwood, which have 50 Ethyl alcohol 11.0 oi ing ranges from 170 C. to 310 C., may be Water 21,0 charged into a vacuum still heated by circulating oil, and fractionated through a plate column Example H Per cent of approximately 15 plates.
- Water I 20 Caustic-soluble hardwood oil may be prepared 60 from the same starting materials, for instance in ,the manner described in the Figg application sodium salts is then treated with carbon dioxide gas to liberate the acidic components as oils, and to convert any free sodium hydroxide present to sodium carbonate and bicarbonate. The oils are then steam distilled from the mixture.
- caustic alkali- may be used instead of sodium hydroxide.
- the alkali acetate remaining in the aqueous solution may be recovered by means of sulfuric acid.
- a liquid, antiseptic toilet soap comprising It will be' understood that another soap, water, hardwood oil whose boiling range is between 180 C. and 240C. in a proportion which would otherwise cause substantial darkening thereof, a blending agent for the soap and the hardwood oil, and a halide selected from the 5 group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium, and magnesium, in sufllcient quantity to prevent the wood oil from darkening in the light and air.
- a liquid, antiseptic toilet soap comprising soap, water, from 0.5% to 33% by volume of hardwood oil whose boiling range is between 180 C. and 240 0., a blending agent for the soap and the hardwood oil, and from 0.20 to 0.30 gram, per 15 100 cubic centimeters, of a halide selected from the group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium.
- a liquid, antiseptic toilet soap comprising 20 soap, water, caustic-soluble hardwood oil in a proportion which would otherwise cause substantial darkening thereof, a blending agent for the. soap and the hardwood oil, and a halide selected from the group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium, in sufiicientquantity to prevent the Wood 011 from darkening inthe light and air.
- a liquid, antiseptic toilet soap comprising", soap, water, from 0.5% to 33% by volume of! caustic-soluble hardwood oil, a blending agent for the soap and the hardwood oil, and from 0.20 to 0.30 gram, per 100 cubic centimeters, of a halide selected from the group consisting oi! the 35 bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium.
- a .iiquid, antiseptic toilet soap comprising soap, water, ethyl alcohol, from 0.5% to 33% by volume of hardwood oil whose boiling range is between 180 C. and 240 0., and from 0.20 to.0.30 gram, per 100 cubic centimeters, of a halide selected from" the group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium.
- a liquid, antiseptic toilet soap comprising soap, water, ethyl alcohol, from 0.5% to 33% by volume of caustic-soluble hardwood oil, and from 0.20 to 0.30 grim, per'100 cubic centimeters, of a halide selected from the group consisting of the bromides and iodides of potassium, sodium,
Description
atente Apr. 4, 1939 2,153,143 nonmsooaorg n i onm ANTISEPTIC Louis J. Figg, Jr., and Edward E. Shaulis, Kingsport, Tenn, assignors to Eastman Kodak Company, heater, N. Y a corporation of New Jersey No Drawing. Application January 28, 1938, Serial No. 187,557
6 Claims. (Cl. 87-5) This invention relates to liquid, antiseptic soap, Example I]! and more particularly to liquid, antiseptic toilet Per cent soap. This application is in part a continuation by volume of our application Serial No. 100,087, filed Sep- Liquid saponified cocoanut oil soap 50.0
tember 9, 1936. Caustic-soluble hardwood oil 15.0 5
In the copending' application of one of us, Essential oils 3.0 Louis J. Figg, Jr., Serial No. 186,099, filed Jan. Ethyl alcohol 11.0 21, 1938, a liquid, antiseptic toilet soap has been Water -Q; 21.0
described, which comprises soap, a hardwood oil,
10 and a blending agent for the soap and the hardxample IV Per 10 good oil. The hardwood oil is purified either 5 b y distillation, only a fraction boiling between 180 C. and 240 C. being used, or by alkali treatgg ggiggggg g ggsgz a g soap ment, only the caustic-soluble portion of the oil Essential Oils 1 being used. Other substances, such, for instance, Ethy1a1coh1"" u 5 15 as pine tar oil and/or essential oils, may al Water be incorporated in the liquid soap. The hardwoodoil may suitably amount to from 0.5% to It will be understood that the proportions are 33%, by l of th liquid antiseptic soa,p by way of illustration only. Among the blending 20 We prefer to use from 5% to 15% of the harde s which We may use, e ay e t o o 20 wood oil. example, in addition to ethyl alcohol: methanol,
Such a soap has been found to darken in P DYI 911001101, isopropyl lcohol, the butyl a1 color in the light and air, because of some change hols, t y alcohols. t yl a tat t yl a ein the hardwood oil, which presumably becomes tote. propyl acetate, s pr p l acetate, the buty oxidized to some xt t, Alth h t darkenacetates, the amyl acetates, acetone, methyl ace- 25 ing does not impair the usefulness of the antitone, m t yl thyl ket n et p py t septic soap, it detracts from its appearance and, e y ketone, methyl ty ketone, dlbutyl hence from its salability, I ketone, methyl amyl ketone, ethylene glycol, pro- One object of our invention is to provide a hyle'ne lycol, di thy ly l, ethylene ly liquid, antiseptic soap containing hardwood oil, monomethyl o e ylene glycol monoethyl 30 which will not darken in the li ht a d i Qther ether, ethylene glycol monobutyl ether, diethylene objects will hereinafter appean glycol monomethyl ether,diethylene glycol mono- We have discovered that if a small amount ethyl ether, and die ene lyco monobuty of a halide selected from the group consisting etherof the iodides and bromides of potassium, sodium, T0 ch a s ap we add, to pr v it caesium, lithium, barium, strontium, calcium and darkening. fr m 0- r m t -30 am. pr magnesium is add d to a, liquid, antiseptic p erably 0.25 gram, of an iodide or bromide of containing a hardwood oil, darkening of the oil, Potassium, Sodium. a t barium. and consequently of the soap, on contact with Strontium calcium or magnesium P 100 light and air is prevented, We have found such amounts to be very eil'ective. 40
As examples of a liquid, antiseptic toilet soa It is best to dissolve the halide in some of the containing a hardwood oil, we give the following Water used in making up he soap comformulae: position, as it' has only a limited solubility in Example I the liquid antiseptic soap. P t Hardwood oil whose boiling range is between 45 by volume 180 C. and 240 C. may be prepared as described Liquid saponifled coooanut oil soap. 50.0 in the Figg application referred to above. Name- Hardwood oils 7.5 hr. the heavy oils and tars which settle out of p nil 7,5 the raw pyroligneous acid resulting from the s ti l oils 3,0 destructive distillation-of hardwood, which have 50 Ethyl alcohol 11.0 oi ing ranges from 170 C. to 310 C., may be Water 21,0 charged into a vacuum still heated by circulating oil, and fractionated through a plate column Example H Per cent of approximately 15 plates. The fraction whose byvolume boiling range at atmospheric pressure is 180}- 55 Liquid saponified cocoanut oil soap 52 240 C., approximately, is collected and re-dis- Hardwood oil=pine-tar oil mixture (1:1)"..- 12 tilled in a vacuum still heated by steam coils, Essential oils 1 the fraction which, at atmospheric pressure, Ethyl alc l5 boils above 180 0. being collected.
Water I 20 Caustic-soluble hardwood oil may be prepared 60 from the same starting materials, for instance in ,the manner described in the Figg application sodium salts is then treated with carbon dioxide gas to liberate the acidic components as oils, and to convert any free sodium hydroxide present to sodium carbonate and bicarbonate. The oils are then steam distilled from the mixture.
-While carbon dioxide liberatesa satisfactory quality of caustic-soluble wood oil, which does not possess certain of the disadvantageous characteristics of caustic-soluble wood oil liberated by sulfuric acid, the use of carbon dioxide is relatively expensive. We have found that the use of acetic acid in place of carbon dioxide produces a wood oil at least 'assatisfactory as that produced by the carbon dioxide treatment, and is considerably more economical. Acetic acid is relatively cheap, and can be recovered, because upon reacting with the sodium salt of the caustic-soluble wood oil, it forms sodium acetate, which can later be decomposed by sulfuric acid to form acetic acid.
By way of illustration of the process in which we use acetic acid to replace either sulfuric acid or carbon dioxide, we give the following example.
To gallons of wood oil, resulting from the destructive distillation of wood and having a caustic solubility of from 50 to 60%, are added 12 gallons of 56% sodium hydroxide solution and 16 gallons of water. The mixture is allowed to stand for one hour. The greater portion of the neutral oil separates, and is withdrawn mechanically. The
- remainder of the neutral oil is removed from the 7 solution of caustic-soluble oil by steam distilla tion. The neutral oil may be discarded or separately stored. To liberate the caustic-soluble oil from the aqueous solution of its sodium salts, 250
lbs. of 56% acetic acid is added. The greater portion'of the oil which separates can be withdrawn mechanically, and the remainder by,steam distillation. caustic alkali-may be used instead of sodium hydroxide. The alkali acetate remaining in the aqueous solution may be recovered by means of sulfuric acid.
What we claim as our invention and desire to be secured by Letters Patent of the United States 1. A liquid, antiseptic toilet soap comprising It will be' understood that another soap, water, hardwood oil whose boiling range is between 180 C. and 240C. in a proportion which would otherwise cause substantial darkening thereof, a blending agent for the soap and the hardwood oil, and a halide selected from the 5 group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium, and magnesium, in sufllcient quantity to prevent the wood oil from darkening in the light and air.
2. A liquid, antiseptic toilet soap comprising soap, water, from 0.5% to 33% by volume of hardwood oil whose boiling range is between 180 C. and 240 0., a blending agent for the soap and the hardwood oil, and from 0.20 to 0.30 gram, per 15 100 cubic centimeters, of a halide selected from the group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium.
3. A liquid, antiseptic toilet soap comprising 20 soap, water, caustic-soluble hardwood oil in a proportion which would otherwise cause substantial darkening thereof, a blending agent for the. soap and the hardwood oil, and a halide selected from the group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium, in sufiicientquantity to prevent the Wood 011 from darkening inthe light and air.
4. A liquid, antiseptic toilet soap comprising", soap, water, from 0.5% to 33% by volume of! caustic-soluble hardwood oil, a blending agent for the soap and the hardwood oil, and from 0.20 to 0.30 gram, per 100 cubic centimeters, of a halide selected from the group consisting oi! the 35 bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium.
.5. A .iiquid, antiseptic toilet soap comprising soap, water, ethyl alcohol, from 0.5% to 33% by volume of hardwood oil whose boiling range is between 180 C. and 240 0., and from 0.20 to.0.30 gram, per 100 cubic centimeters, of a halide selected from" the group consisting of the bromides and iodides of potassium, sodium, caesium, lithium, barium, strontium, calcium and magnesium.
6. A liquid, antiseptic toilet soap comprising soap, water, ethyl alcohol, from 0.5% to 33% by volume of caustic-soluble hardwood oil, and from 0.20 to 0.30 grim, per'100 cubic centimeters, of a halide selected from the group consisting of the bromides and iodides of potassium, sodium,
' caesium, lithium,'barium, strontium, calcium and magnesium.
LOUIS J. FIGG, JRJ'.
EDWARD E. SHAULIS.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US187557A US2153143A (en) | 1938-01-28 | 1938-01-28 | Nondiscoloring, liquid antiseptic soap |
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US187557A US2153143A (en) | 1938-01-28 | 1938-01-28 | Nondiscoloring, liquid antiseptic soap |
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US187557A Expired - Lifetime US2153143A (en) | 1938-01-28 | 1938-01-28 | Nondiscoloring, liquid antiseptic soap |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2507649A (en) * | 1947-04-29 | 1950-05-16 | Universal Oil Prod Co | Treatment of wood tar distillates |
US4589994A (en) * | 1984-12-17 | 1986-05-20 | Moseman Roger E | Liquid foot treatment composition |
US4668419A (en) * | 1984-12-17 | 1987-05-26 | Moseman Roger E | Liquid foot treatment composition |
US5908619A (en) * | 1997-01-09 | 1999-06-01 | Minnesota Mining And Manufacturing Company | Hydroalcoholic compositions thickened using surfactant/polymer complexes |
US5951993A (en) * | 1995-06-22 | 1999-09-14 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
US6019997A (en) * | 1997-01-09 | 2000-02-01 | Minnesota Mining And Manufacturing | Hydroalcoholic compositions for transdermal penetration of pharmaceutical agents |
US6090395A (en) * | 1995-06-22 | 2000-07-18 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
US6582711B1 (en) | 1997-01-09 | 2003-06-24 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
US6623744B2 (en) * | 1995-06-22 | 2003-09-23 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US20060263396A1 (en) * | 1995-06-22 | 2006-11-23 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US20110175509A1 (en) * | 2010-01-18 | 2011-07-21 | Remis Gesellschaft Fuer Entwicklung Und Vertrieb Technischer Elemente Mbh | Refrigerated cabinet with door assembly |
-
1938
- 1938-01-28 US US187557A patent/US2153143A/en not_active Expired - Lifetime
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2507649A (en) * | 1947-04-29 | 1950-05-16 | Universal Oil Prod Co | Treatment of wood tar distillates |
US4589994A (en) * | 1984-12-17 | 1986-05-20 | Moseman Roger E | Liquid foot treatment composition |
US4668419A (en) * | 1984-12-17 | 1987-05-26 | Moseman Roger E | Liquid foot treatment composition |
US6534069B1 (en) | 1995-06-22 | 2003-03-18 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US5951993A (en) * | 1995-06-22 | 1999-09-14 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
US7803390B2 (en) | 1995-06-22 | 2010-09-28 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US6090395A (en) * | 1995-06-22 | 2000-07-18 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
US6352701B1 (en) | 1995-06-22 | 2002-03-05 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US7081246B2 (en) * | 1995-06-22 | 2006-07-25 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US6562360B2 (en) | 1995-06-22 | 2003-05-13 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US7566460B2 (en) | 1995-06-22 | 2009-07-28 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US6610315B2 (en) | 1995-06-22 | 2003-08-26 | 3M Innovative Properties Company | Topical application of stable hydroalcoholic compositions for maintaining or improving skin conditions, and delivering fragrance to skin |
US6623744B2 (en) * | 1995-06-22 | 2003-09-23 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US20060263396A1 (en) * | 1995-06-22 | 2006-11-23 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US20040071748A1 (en) * | 1995-06-22 | 2004-04-15 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US20060121071A1 (en) * | 1995-06-22 | 2006-06-08 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US6019997A (en) * | 1997-01-09 | 2000-02-01 | Minnesota Mining And Manufacturing | Hydroalcoholic compositions for transdermal penetration of pharmaceutical agents |
US20030215418A1 (en) * | 1997-01-09 | 2003-11-20 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
US6582711B1 (en) | 1997-01-09 | 2003-06-24 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
US5908619A (en) * | 1997-01-09 | 1999-06-01 | Minnesota Mining And Manufacturing Company | Hydroalcoholic compositions thickened using surfactant/polymer complexes |
US8062649B2 (en) | 1997-01-09 | 2011-11-22 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
US20110175509A1 (en) * | 2010-01-18 | 2011-07-21 | Remis Gesellschaft Fuer Entwicklung Und Vertrieb Technischer Elemente Mbh | Refrigerated cabinet with door assembly |
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