US2035494A - Perfume-emitting materials - Google Patents
Perfume-emitting materials Download PDFInfo
- Publication number
- US2035494A US2035494A US701569A US70156933A US2035494A US 2035494 A US2035494 A US 2035494A US 701569 A US701569 A US 701569A US 70156933 A US70156933 A US 70156933A US 2035494 A US2035494 A US 2035494A
- Authority
- US
- United States
- Prior art keywords
- perfume
- bisulfite
- aldehyde
- odor
- water
- 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
- 239000000463 material Substances 0.000 title description 16
- 239000002304 perfume Substances 0.000 description 26
- 239000000344 soap Substances 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 13
- 239000000843 powder Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 150000001299 aldehydes Chemical class 0.000 description 12
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 12
- 235000019645 odor Nutrition 0.000 description 12
- 150000002576 ketones Chemical class 0.000 description 10
- -1 bisulfite compound Chemical class 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 6
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 244000144725 Amygdalus communis Species 0.000 description 4
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 4
- 229940043350 citral Drugs 0.000 description 4
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 4
- 235000003893 Prunus dulcis var amara Nutrition 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- NZGWDASTMWDZIW-MRVPVSSYSA-N (+)-pulegone Chemical compound C[C@@H]1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-MRVPVSSYSA-N 0.000 description 2
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 2
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 2
- 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 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 229940117916 cinnamic aldehyde Drugs 0.000 description 2
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 2
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 229930002839 ionone Natural products 0.000 description 2
- 150000002499 ionone derivatives Chemical class 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 2
- 235000019801 trisodium phosphate Nutrition 0.000 description 2
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 244000166675 Cymbopogon nardus Species 0.000 description 1
- 235000018791 Cymbopogon nardus Nutrition 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- UZFLPKAIBPNNCA-UHFFFAOYSA-N alpha-ionone Natural products CC(=O)C=CC1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- XGRNEMYYNQFOGN-UHFFFAOYSA-N benzaldehyde;sulfurous acid Chemical compound OS(O)=O.O=CC1=CC=CC=C1 XGRNEMYYNQFOGN-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229930003633 citronellal Natural products 0.000 description 1
- 235000000983 citronellal Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- UZFLPKAIBPNNCA-FPLPWBNLSA-N α-ionone Chemical compound CC(=O)\C=C/C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-FPLPWBNLSA-N 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
- C11D9/44—Perfumes; Colouring materials; Brightening agents ; Bleaching agents
- C11D9/442—Perfumes
Definitions
- This invention relates to a novel method of increasing the cost thereof. For instance when,
- perfume was added to ordinary'soap it was necessary to add about one percent by weight in order that it would not be completely dissipated before the soap was used. In the case of fine soaps about two to three percent of perfume was added. Obviously this increased appreciably the cost of production, and made its use in low priced cleansers prohibitive. As is well known such cleansers possess a disagreeable odor, and would be much more acceptable if it were possible to mask suchodor with a pleasant-smelling perfume.
- a further object is to prevent suchperfumes from being dissipated prior to use. nomically possible to use such compolmds in'low priced cleansers in order that the disagreeable odor thereof will be completely masked. Additional objects will become apparentfrom a consideration of the following description.
- Example 1 To i000 parts of soap powder were added 2 parts of finely powdered benzaldehyde bisulflte compound. The substances were thoroughly mixed. The soap powder remained substantially unperfumed. A small amount (about 1 gram) of the mixture was added to a little water in a beaker, on touching the water the pleasant odor of bitter almonds became at once-noticeable and masked effectively the unpleasant odor of the soap powder A still further object is to make it ecosolution which was quite pronounced in a similar experiment where the benzaldehyde bisulflte compound had been left out. The use of cold or hot water gave the same improved result.
- Example 2 A mixture of 1000 parts of soap powder and 3 parts benzaldehyde bisulflte was tested in household work (cleaning of dishes). The unpleasant odor of the soap powder was found to be successfully covered by a pleasant odor of bitter almond.
- Example 3 Citral was transformed into normal citral bisulilte by treating with sodium sulilte and sodium bicarbonate. 3 parts of n this compound imparted a very pleasant lemon odor to 1000 parts of soap powder as soon as the mixture was brought into contact with water.
- Example 5 The b isulflte compound of heptylic aldehyde was added to soap powder in the proportion of 5 parts per 1000. In the presence of water the characteristic note of oenanthol appeared at once.
- Example 6 The ketone, alpha ionone, was transformed into its crystallized blsulflte derivative and incorporated into soap powder. A concentration of 3 parts to 1000 parts was suflicient to give a scent of violet to the powder upon addition of water.
- Example 7 By replacing the soap powder in Example 1 with anhydroussoda ash a mixture was obtained which.v in water developed the perfume of bitter almonds.-
- alkaline materials other compounds such ashore:- and triscdium phosphatemay housed wlthsatia factory resutts.
- aldehyde and ketone perfumes may be used with excellent results.
- These compounds may be members of the aromatic, aliphatic, isocyclic or heterocyclic series, the only requirement being that they possess odor and are capable of forming bisulfite derivatives from which the original odor-emitting compound may be regenerated by the action of an aqueous alkali.
- citral citronella
- hydroxycitronella benzaldehyde
- cinnamic aldehyde heptylic aldehyde
- pulegon ionone and methyl-ionone.
- Bisulfite derivatives of the various aldehyde and ketone perfumes may readily be prepared by reacting the perfume with the bisulfite compound
- compositions described herein be prepared and maintained in an anhydrous condition until ready for use.
- the material to be perfumed should have sufficient alkalinity to decompose the bisulfite compounds and regenerate the original perfume upon the addition of water. Soap powders and flakes when substantially water-free are excellent illustrations of such media, and may be used with very satisfactory results. However, the invention is not limited thereto since many other compounds possess the property of regenerating the original perfume upon the addition of water. Among these compounds mention may be made of soda ash, .borax, sodium resinate, and trisodium phosphate, it being understood that these materials are representative only of the largegroup of substances possessing this characteristic.
- Bisulflte derivatives of perfumes have never before been incorporated with alkaline materials in order to impart odor thereto since such derivatives are well known to be odorless.
- this odorless property is utilized in a novel manner to produce the exceedingly advantageous result of conserving the perfume until it is actually used.
- the amount of the bisulfite derivatives utilized is so exceedingly small the perfumeemitting properties of thematerials are highly satisfactory since such properties are conserved practically undiminished .until actual use.
- aldehydes and ketones were possessed of very strong and pleasant odors their use in alkaline media such as soaps was formerly not recommended because of their susceptibility to oxidation, polymerization or disintegration in.
- the amount of perfume derivative added according to the present invention is capable of considerable variation and modification. In general 2-5 parts of such derivative per 1000 parts of material to be perfumed give satisfactory results. However, such figures are not to be construed as a restriction since they may be varied within much wider limits without departing from the scope of the present invention. The amount added will depend to a great extent upon the material in which it is to be incorporated and theparticular perfume derivative utilized, and may vary from a trace to as high as several percent. It is, of course, apparent that the bisulfite derivatives of more than one aldehyde and/or ketone perfume may be incorporated into any given material. Two or more of such derivatives may be incorporated in order that the resulting odor-emitting properties will be a blend of the individual odors of the several components.
- a process for producing perfume-emitting materials which comprises forming the bisulfite compound of a member selected from the group consisting of aldehyde and ketone perfumes and adding said bisulfite compound to an alkaline detergent capable of liberating the original perfume upon addition of water, the aforementioned compounds being in a substantially anhydrous condition.
- Aprocess for producing perfume-emitting materials which comprises forming the bisulfite compound 'of a member selected from the group consisting of aldehyde and ketone perfumes and adding said bisulfite compound to a member selected from the group consisting of soap powder, soda ash, borax, and trisodium-phosphate, the aforementioned compounds being in a substantially anhydrous condition.
- perfume derivative is selected from the group consisting of bisulfite-compounds of citral, citronellal, hydroxycitronella, benzaldehyde, cinnamic aldehyde, heptylic aldehyde, pulegon, ionone, and methylionone.
- Perfume-emitting materials which comprise the bisulfite compound of a member selected from the group consisting of aldehyde and ketone perfumes in admixture with an alkaline detergent capable of liberating the original perfume upon addition of water.
- Substantially dry perfume-emitting materials which comprise the bisulfite compound of a member selected from the group consisting of aldehyde and ketone perfumes in admixture with a mem- 8.
- Materials capable of emitting perfume uponwetting which comprise the reaction product of benzaldehyde and sodium bisulfite in admixture with analkaline soap.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
- Detergent Compositions (AREA)
Description
Patented Mar. 31, 1936 UNITED STATES PATENT OFFICE PERFUME-EMITTING MATERIALS Walter Christian Meuly, New Brunswick, N. .L.
assignor to El. du Pont de Nemours & Compony. Wilmington, Del., a corporation of Delaware No Drawing. Application December 8, 1933, Serial No. 701,569
8 Claim.
This invention relates to a novel method of increasing the cost thereof. For instance when,
perfume was added to ordinary'soap it was necessary to add about one percent by weight in order that it would not be completely dissipated before the soap was used. In the case of fine soaps about two to three percent of perfume was added. Obviously this increased appreciably the cost of production, and made its use in low priced cleansers prohibitive. As is well known such cleansers possess a disagreeable odor, and would be much more acceptable if it were possible to mask suchodor with a pleasant-smelling perfume.
It is an object of this invention to permit the use of perfumes in cleansing media and other alkaline material in much smaller quantities than was heretfore possible. A further object is to prevent suchperfumes from being dissipated prior to use. nomically possible to use such compolmds in'low priced cleansers in order that the disagreeable odor thereof will be completely masked. Additional objects will become apparentfrom a consideration of the following description.
'll'hese objects are attained according to the herein described invention which in its preferred embodiment comprises incorporating a small amount of the bisulflte derivative of an aldehyde or ketone perfume in a substantially dry alkaline medium which is capable of liberating the original perfume upon addition of water.
we invention may be more readily understood by a consideration of the following illustrative examples, in which the quantities are stated in parts by weight.
Example 1 To i000 parts of soap powder were added 2 parts of finely powdered benzaldehyde bisulflte compound. The substances were thoroughly mixed. The soap powder remained substantially unperfumed. A small amount (about 1 gram) of the mixture was added to a little water in a beaker, on touching the water the pleasant odor of bitter almonds became at once-noticeable and masked effectively the unpleasant odor of the soap powder A still further object is to make it ecosolution which was quite pronounced in a similar experiment where the benzaldehyde bisulflte compound had been left out. The use of cold or hot water gave the same improved result.
The mixture of soap powder and benzaldehyde bisulfite was kept for 6 months to test the stability of the combination. When brought into contact with water, the almond odor was noted in undiminished strength. I
Example 2 A mixture of 1000 parts of soap powder and 3 parts benzaldehyde bisulflte was tested in household work (cleaning of dishes). The unpleasant odor of the soap powder was found to be successfully covered by a pleasant odor of bitter almond.
Example 3 Example 4 Citral was transformed into normal citral bisulilte by treating with sodium sulilte and sodium bicarbonate. 3 parts of n this compound imparted a very pleasant lemon odor to 1000 parts of soap powder as soon as the mixture was brought into contact with water.
Example 5 The b isulflte compound of heptylic aldehyde was added to soap powder in the proportion of 5 parts per 1000. In the presence of water the characteristic note of oenanthol appeared at once.
Example 6 The ketone, alpha ionone, was transformed into its crystallized blsulflte derivative and incorporated into soap powder. A concentration of 3 parts to 1000 parts was suflicient to give a scent of violet to the powder upon addition of water.
Example 7 By replacing the soap powder in Example 1 with anhydroussoda ash a mixture was obtained which.v in water developed the perfume of bitter almonds.-
In place of or in addition to the foregoing... alkaline materials other compoundssuch ashore):- and triscdium phosphatemay housed wlthsatia factory resutts.
. class of these compounds, and are not intended as a limitation upon the scope of this invention. In place of these compounds numerous other aldehyde and ketone perfumes may be used with excellent results. These compounds may be members of the aromatic, aliphatic, isocyclic or heterocyclic series, the only requirement being that they possess odor and are capable of forming bisulfite derivatives from which the original odor-emitting compound may be regenerated by the action of an aqueous alkali. A few of the compounds falling within this category are citral, citronella, hydroxycitronella, benzaldehyde, cinnamic aldehyde, heptylic aldehyde, pulegon, ionone and methyl-ionone.
Bisulfite derivatives of the various aldehyde and ketone perfumes may readily be prepared by reacting the perfume with the bisulfite compound,
. preferably an alkali-metal bisulfite. These com pounds are incorporated inthe alkaline medium in the dry state. The alkaline medium should also be substantially dry in order that the perfume derivatives will remain unchanged until used. It is advisable that the compositions described herein be prepared and maintained in an anhydrous condition until ready for use.
The material to be perfumed should have sufficient alkalinity to decompose the bisulfite compounds and regenerate the original perfume upon the addition of water. Soap powders and flakes when substantially water-free are excellent illustrations of such media, and may be used with very satisfactory results. However, the invention is not limited thereto since many other compounds possess the property of regenerating the original perfume upon the addition of water. Among these compounds mention may be made of soda ash, .borax, sodium resinate, and trisodium phosphate, it being understood that these materials are representative only of the largegroup of substances possessing this characteristic.
Bisulflte derivatives of perfumes have never before been incorporated with alkaline materials in order to impart odor thereto since such derivatives are well known to be odorless. By means of the instant invention this odorless property is utilized in a novel manner to produce the exceedingly advantageous result of conserving the perfume until it is actually used. Despite the fact that the amount of the bisulfite derivatives utilized is so exceedingly small the perfumeemitting properties of thematerials are highly satisfactory since such properties are conserved practically undiminished .until actual use. Furthermore, although aldehydes and ketones were possessed of very strong and pleasant odors their use in alkaline media such as soaps was formerly not recommended because of their susceptibility to oxidation, polymerization or disintegration in.
the presence of such media. In the form of the bisulfite compounds however they may be kept in contact with alkaline materials practically indefinitely, without destroying to any noticeable extent their valuable odor-emitting properties.
It is to be understood that the amount of perfume derivative added according to the present invention is capable of considerable variation and modification. In general 2-5 parts of such derivative per 1000 parts of material to be perfumed give satisfactory results. However, such figures are not to be construed as a restriction since they may be varied within much wider limits without departing from the scope of the present invention. The amount added will depend to a great extent upon the material in which it is to be incorporated and theparticular perfume derivative utilized, and may vary from a trace to as high as several percent. It is, of course, apparent that the bisulfite derivatives of more than one aldehyde and/or ketone perfume may be incorporated into any given material. Two or more of such derivatives may be incorporated in order that the resulting odor-emitting properties will be a blend of the individual odors of the several components.
As many apparently widely difierent embodiments of this invention maybe made without departing from the spirit and scope thereof, it is to be understood that the invention is not limited to the specific embodiments thereof except as defined in the appended claims.
I claim:
1. A process for producing perfume-emitting materials which comprises forming the bisulfite compound of a member selected from the group consisting of aldehyde and ketone perfumes and adding said bisulfite compound to an alkaline detergent capable of liberating the original perfume upon addition of water, the aforementioned compounds being in a substantially anhydrous condition.
2, Aprocess for producing perfume-emitting materials which comprises forming the bisulfite compound 'of a member selected from the group consisting of aldehyde and ketone perfumes and adding said bisulfite compound to a member selected from the group consisting of soap powder, soda ash, borax, and trisodium-phosphate, the aforementioned compounds being in a substantially anhydrous condition.
3. The process of claim 2 wherein the perfume derivative is selected from the group consisting of bisulfite-compounds of citral, citronellal, hydroxycitronella, benzaldehyde, cinnamic aldehyde, heptylic aldehyde, pulegon, ionone, and methylionone.
4. Perfume-emitting materials which comprise the bisulfite compound of a member selected from the group consisting of aldehyde and ketone perfumes in admixture with an alkaline detergent capable of liberating the original perfume upon addition of water.
5. Substantially dry perfume-emitting materials which comprise the bisulfite compound of a member selected from the group consisting of aldehyde and ketone perfumes in admixture with a mem- 8. Materials capable of emitting perfume uponwetting which comprise the reaction product of benzaldehyde and sodium bisulfite in admixture with analkaline soap.
, WALTER C. MIEULY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US701569A US2035494A (en) | 1933-12-08 | 1933-12-08 | Perfume-emitting materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US701569A US2035494A (en) | 1933-12-08 | 1933-12-08 | Perfume-emitting materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2035494A true US2035494A (en) | 1936-03-31 |
Family
ID=24817870
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US701569A Expired - Lifetime US2035494A (en) | 1933-12-08 | 1933-12-08 | Perfume-emitting materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2035494A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5710122A (en) * | 1995-12-20 | 1998-01-20 | The Procter & Gamble Company | Sulfonate derivatized perfumes |
-
1933
- 1933-12-08 US US701569A patent/US2035494A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5710122A (en) * | 1995-12-20 | 1998-01-20 | The Procter & Gamble Company | Sulfonate derivatized perfumes |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3779932A (en) | Solid washing compositions | |
| US3629121A (en) | Carboxylated starches as detergent builders | |
| US4191660A (en) | Organoleptic uses of 1-(3,3-dimethyl-2-norbornyl)-2-propanone in cationic, anionic and nonionic detergents and soaps | |
| USRE27332E (en) | Perfume compositions containing geranonitrile, cinnamyl nitrile or z-nonenyl nitrile | |
| US2374187A (en) | Detergent composition | |
| US3668134A (en) | Detergent compositions containing the ethers and esters of tetrahydrofuran and tetrahydropyran | |
| US2196150A (en) | Tooth powder | |
| JPH01256597A (en) | Powdered detergent composition | |
| US1621906A (en) | Cleansing compound | |
| US3326746A (en) | 1, 3-dioxane cleaning compositions | |
| US3860525A (en) | Cleaning composition with stabilized perfume | |
| US3755179A (en) | Chemical composition | |
| US2035494A (en) | Perfume-emitting materials | |
| US3030310A (en) | Combination soap-synthetic detergent bar | |
| US3803244A (en) | Acetals of 2-alkyl-3-norbornyl propanals | |
| US3947574A (en) | Solid sterilizing compositions | |
| US1716000A (en) | Manufacture of soap | |
| US3928247A (en) | Novel perfumery uses of {90 -cyanotricyclene | |
| US4040986A (en) | Preparation of 4-methoxybenzonitrile perfume compositions | |
| US4351347A (en) | Organoleptic uses of norbornyl ethers and esters | |
| JPH01185400A (en) | Method of imparting odor to powdery alkali detergent | |
| JPS62283913A (en) | Perfume composition | |
| US1531324A (en) | Detergent | |
| DE2132898A1 (en) | Foam-suppressing additives - for washing- cleaning - or water-softening compsns- selected from acetals, ketals and mercaptals | |
| US4390464A (en) | Methyl substituted norbornane derivatives, organoleptic uses thereof and process for preparing same |