US2425118A - Dental impression composition - Google Patents
Dental impression composition Download PDFInfo
- Publication number
- US2425118A US2425118A US591221A US59122145A US2425118A US 2425118 A US2425118 A US 2425118A US 591221 A US591221 A US 591221A US 59122145 A US59122145 A US 59122145A US 2425118 A US2425118 A US 2425118A
- Authority
- US
- United States
- Prior art keywords
- composition
- zinc nitrate
- alcohol
- sodium
- 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
- 239000000203 mixture Substances 0.000 title description 24
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 235000019441 ethanol Nutrition 0.000 description 12
- 235000010443 alginic acid Nutrition 0.000 description 11
- 229920000615 alginic acid Polymers 0.000 description 11
- 239000000499 gel Substances 0.000 description 11
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 10
- 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 8
- 239000000463 material Substances 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- -1 alkali metal salts Chemical class 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 229940072056 alginate Drugs 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000783 alginic acid Substances 0.000 description 3
- 229960001126 alginic acid Drugs 0.000 description 3
- 150000004781 alginic acids Chemical group 0.000 description 3
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 3
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 3
- 239000011507 gypsum plaster Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- SNXYIOIMZXSIDC-UHFFFAOYSA-A hexadecasodium;phosphonato phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O SNXYIOIMZXSIDC-UHFFFAOYSA-A 0.000 description 3
- 235000010408 potassium alginate Nutrition 0.000 description 3
- 239000000737 potassium alginate Substances 0.000 description 3
- MZYRDLHIWXQJCQ-YZOKENDUSA-L potassium alginate Chemical compound [K+].[K+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O MZYRDLHIWXQJCQ-YZOKENDUSA-L 0.000 description 3
- 235000010413 sodium alginate Nutrition 0.000 description 3
- 239000000661 sodium alginate Substances 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- 241000206672 Gelidium Species 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004110 Zinc silicate Substances 0.000 description 2
- 235000010419 agar Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011505 plaster Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- XSMMCTCMFDWXIX-UHFFFAOYSA-N zinc silicate Chemical compound [Zn+2].[O-][Si]([O-])=O XSMMCTCMFDWXIX-UHFFFAOYSA-N 0.000 description 2
- 235000019352 zinc silicate Nutrition 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- 241000512259 Ascophyllum nodosum Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000206576 Chondrus Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000227647 Fucus vesiculosus Species 0.000 description 1
- 241001467355 Gigartina Species 0.000 description 1
- 241000206581 Gracilaria Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- SNVQVLIHTDFQDH-UHFFFAOYSA-L [Li+].P(=O)(O)([O-])[O-].[Na+] Chemical compound [Li+].P(=O)(O)([O-])[O-].[Na+] SNVQVLIHTDFQDH-UHFFFAOYSA-L 0.000 description 1
- 235000010407 ammonium alginate Nutrition 0.000 description 1
- 239000000728 ammonium alginate Substances 0.000 description 1
- KPGABFJTMYCRHJ-YZOKENDUSA-N ammonium alginate Chemical compound [NH4+].[NH4+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O KPGABFJTMYCRHJ-YZOKENDUSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002978 dental impression material Substances 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 229940093474 manganese carbonate Drugs 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/90—Compositions for taking dental impressions
Definitions
- This invention relates to a new dental impression compound and the method of producing the same.
- an impression material which may be introduced in the mouth in a fluid or plastic condition and cooled to an elastic state, it is possible to take an impression which will accurately reproduce all details of the portion of the mouth under examination, and which due to its elasticity, can be removed from any undercuts present without losing the accuracy of the impression.
- My dental impression material is composed of a suitable gel forming agent which may be obtained, for example, from the various marine algae in-'- cluding gigartina, chondrus, bladder wrack, kelp, gracilaria, or agar-agar. If the gel forming agent is alginic acid it may be converted into the form 'of a salt, as for example, sodium alginate, potassium alginate, ammonium alginate or mixtures thereof. The salts of alginic acid are used in the impression material to render the product elastic.
- a heavy metal silicate such as for example lead silicate or zinc silicate.
- a heavy metal silicate such as for example lead silicate or zinc silicate.
- the exact chemical reaction which takes place on the addition of the lead or zinc silicate to the dental composition is not fully understood but it is definitely known to affect the conversion of the gel forming agent from the soluble to the insoluble form. For example water soluble alkali metal salts of alginic acid are converted over to the insoluble form.
- a water soluble phosphate such as sodium, potassium or lithium phosphate sodium hexametaphosphate may also be employed.
- Sodium tetrapyrophosphate has also been found to be especially satisfactory by reason of its limited solubility in Water.
- Zinc nitrate is also added to my composition to produce an insoluble compound with the gel forming constituents such as the alginates.
- the ordinary commercia] U. S. P. zinc nitrate may be used but in order to control the action of the zinc nitrate it has been found advantageous to pretreat the zinc nitrate in the following manner.
- the zinc nitrate is first dissolved in a low boiling aliphatic alcohol such as ethyl or methyl alcohol and this solution is evaporated at a temperature of about 200 F. until all of the alcohol present has been vaporized.
- the resulting residue is then Water Washed, dried and ground. Again it is not understood exactly why the zinc nitrate pretreated in the above manner is aliected. It is definitely known, however, that the Zinc nitrate pretreated with alcohol, as described above is less water soluble and reacts more slowly with the gel forming agent (for example sodium or potassium alginate).
- the gel forming agent for example sodium or potassium alginate
- a filler such as diatomaceous earth, manganese carbonate, or talc which is insoluble in water and which is easily Wetted.
- the blended material is then withdrawn from the tumbling or mixing device and thoroughly mixed with 50 cubic centimeters of water with a spatula until, a smooth creamy mixture is obtained which sets in a short time to an elastic gel.
- this creamy mixture is placed in a dental tray which is placed in the mouth of the patient where it sets up in the form of the elastic gel in from three to six minutes.
- the setting time can be varied by varying the temperature of the Water used. Cold water will retard the set and warm water will hasten it. This control can also be maintained by varying the amount of the powdered composition used in combination with water. The greater amount of powder used in relationshi to the water the more time will be required to obtain the proper set.
- An impression containing the above composition can be removed from the mouth after setting without breaking, tearing or distorting and will allow dental stone or plaster of Paris to set hard against its surface with extreme accuracy.
- This impression material also possesses the quality of not requiring a separating medium or fixing bath before pouring dental stone or plaster of Paris into the impression. Furthermore, it can be stored over a long period without deteriorating.
- composition of matter comprising an alkali metal alginate, lead silicate and zinc nitrate, which has been dissolved in a lower aliphatic alcohol and recovered therefrom by evaporation of the alcohol.
- composition of matter comprising an alkali metal alginate, lead silicate, sodium fiuosilicate and zinc nitrate which has been rendered substantitally insoluble in water by treatment with a lower aliphatic alcohol.
- a composition of matter comprising an alkali metal alginate, lead silicate, sodium fluosilicate, an inorganic phosphate salt, and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.
- composition of matter comprising an alkali metal alginate, lead silicate and zinc nitrate which is substantially insoluble in water.
- a composition of matter comprising a gel forming material selected from the class consistingof alginates and agar-agar, lead silicate and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.
- a composition of matter comprising an alkali metal alginate, a heavy metal silicate, and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.
- a composition of matter comprising an alkali metal alginate, a heavy metal silicate, sodium fiuosilicate, sodium tetra pyrophosphate a filler and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol at a temperature not substantially in excess of 200 F.
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dental Preparations (AREA)
Description
Patented Aug. 5, 1947 DENTAL IMPRESSION COMPOSITION Stanley E. Noyes, Los Angeles, Calif.
No Drawing. Application April 30, 1945, Serial No. 591,221
7 Claims. (01. 18-47) This invention relates to a new dental impression compound and the method of producing the same.
For many dental purposes such as making of full dentures, partial dentures, bridges, etc., it is necessary for the dentist to be able to accurately reproduce portions of the mouth of the subject. Such reproductions often involve the duplication of undercuts of more or less severity, as for instance in the case where a tooth or teeth have been extracted and the adjacent teeth have crowded together.
For many years dental impressions have been taken with materials such as plaster of Paris, or various shellac or wax compositions. These materials have little or no elasticity and. while it is not difficult to take some impressions with them, such as for most full dentures, it is not possible to reproduce accurately undercuts without either breaking the impression and i e-assembling it as is done with plaster, or taking the impression in sections as is the practice in the use ofshellac and Wax compounds. The foregoing methods obviously involve time and there is the danger of inaccuracy, as well as discomfort to the patient.
By the use of an impression material which may be introduced in the mouth in a fluid or plastic condition and cooled to an elastic state, it is possible to take an impression which will accurately reproduce all details of the portion of the mouth under examination, and which due to its elasticity, can be removed from any undercuts present without losing the accuracy of the impression.
Due to the narrow range of temperature which the human mouth can stand, rather strict limitations are placed on the types of elastic materials which can be used. These materials must obviously be either fluid or plastic when they are seated to place in the mouth and must change by cooling to an elastic gel which will permit removal from the undercuts without permanent distortion. They must also either harden to a solid or be a sufficiently tough and rigid gel so that they may be used as molds for models of plaster or other compounds to be poured into them.
My dental impression material is composed of a suitable gel forming agent which may be obtained, for example, from the various marine algae in-'- cluding gigartina, chondrus, bladder wrack, kelp, gracilaria, or agar-agar. If the gel forming agent is alginic acid it may be converted into the form 'of a salt, as for example, sodium alginate, potassium alginate, ammonium alginate or mixtures thereof. The salts of alginic acid are used in the impression material to render the product elastic.
To the gel forming agent then is added a heavy metal silicate such as for example lead silicate or zinc silicate. The exact chemical reaction which takes place on the addition of the lead or zinc silicate to the dental composition is not fully understood but it is definitely known to affect the conversion of the gel forming agent from the soluble to the insoluble form. For example water soluble alkali metal salts of alginic acid are converted over to the insoluble form.
To the foregoing composition then is also added a water soluble phosphate such as sodium, potassium or lithium phosphate sodium hexametaphosphate may also be employed. Sodium tetrapyrophosphate has also been found to be especially satisfactory by reason of its limited solubility in Water.
To the foregoing composition then is also added sodium fiuosilicate, however other silico fluorides may be used as for example zinc, manganese, or calcium.
Zinc nitrate is also added to my composition to produce an insoluble compound with the gel forming constituents such as the alginates. The ordinary commercia] U. S. P. zinc nitrate may be used but in order to control the action of the zinc nitrate it has been found advantageous to pretreat the zinc nitrate in the following manner. The zinc nitrate is first dissolved in a low boiling aliphatic alcohol such as ethyl or methyl alcohol and this solution is evaporated at a temperature of about 200 F. until all of the alcohol present has been vaporized. The resulting residue is then Water Washed, dried and ground. Again it is not understood exactly why the zinc nitrate pretreated in the above manner is aliected. It is definitely known, however, that the Zinc nitrate pretreated with alcohol, as described above is less water soluble and reacts more slowly with the gel forming agent (for example sodium or potassium alginate).
To the above composition there is finally added a filler such as diatomaceous earth, manganese carbonate, or talc which is insoluble in water and which is easily Wetted.
The following is a specific example of my new dental composition: 10 grams of diatomaceous earth, 1.75 grams of sodium fluosilicate, 4.0 grams of sodium or potassium alginate, 6.75 grams of lead silicate, 0.5 gram of sodium tetrapyrophosphate and 0.5 gram of zinc nitrate (either as purchased in the U. S. P. form or pretreated with alcohol as described above) are placed in a finely divided and dry form in a tumbling keg or mixer and mixed until a uniform blend is obtained. This mixing should be so conducted that the temperature in the tumbler or mixing device does not exceed 100 to 110 F., otherwise the final composition may be damaged. The blended material is then withdrawn from the tumbling or mixing device and thoroughly mixed with 50 cubic centimeters of water with a spatula until, a smooth creamy mixture is obtained which sets in a short time to an elastic gel. In practice this creamy mixture is placed in a dental tray which is placed in the mouth of the patient where it sets up in the form of the elastic gel in from three to six minutes. The setting time can be varied by varying the temperature of the Water used. Cold water will retard the set and warm water will hasten it. This control can also be maintained by varying the amount of the powdered composition used in combination with water. The greater amount of powder used in relationshi to the water the more time will be required to obtain the proper set.
An impression containing the above composition can be removed from the mouth after setting without breaking, tearing or distorting and will allow dental stone or plaster of Paris to set hard against its surface with extreme accuracy. This impression material also possesses the quality of not requiring a separating medium or fixing bath before pouring dental stone or plaster of Paris into the impression. Furthermore, it can be stored over a long period without deteriorating.
The specific mixture of ingredients set forth above in the example can be modified without departing from the spirit of the invention.
I claim:
1. A composition of matter comprising an alkali metal alginate, lead silicate and zinc nitrate, which has been dissolved in a lower aliphatic alcohol and recovered therefrom by evaporation of the alcohol.
2. A composition of matter comprising an alkali metal alginate, lead silicate, sodium fiuosilicate and zinc nitrate which has been rendered substantitally insoluble in water by treatment with a lower aliphatic alcohol.
3. A composition of matter comprising an alkali metal alginate, lead silicate, sodium fluosilicate, an inorganic phosphate salt, and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.
4. A composition of matter comprising an alkali metal alginate, lead silicate and zinc nitrate which is substantially insoluble in water.
5. A composition of matter comprising a gel forming material selected from the class consistingof alginates and agar-agar, lead silicate and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.
6. A composition of matter comprising an alkali metal alginate, a heavy metal silicate, and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.
7. A composition of matter comprising an alkali metal alginate, a heavy metal silicate, sodium fiuosilicate, sodium tetra pyrophosphate a filler and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol at a temperature not substantially in excess of 200 F.
STANLEY E. NOYES.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,249,694 Wilding July 15, 1941 2,298,835 Noyes Oct. 13, 1942 2,325,051 Gross July 2'7, 1943
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US591221A US2425118A (en) | 1945-04-30 | 1945-04-30 | Dental impression composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US591221A US2425118A (en) | 1945-04-30 | 1945-04-30 | Dental impression composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2425118A true US2425118A (en) | 1947-08-05 |
Family
ID=24365593
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US591221A Expired - Lifetime US2425118A (en) | 1945-04-30 | 1945-04-30 | Dental impression composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2425118A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2568752A (en) * | 1947-07-28 | 1951-09-25 | Dental Perfection Company | Dental impression composition |
| US2678280A (en) * | 1952-03-21 | 1954-05-11 | Dental Perfection Company | Gel point indicating impression materials |
| US2681860A (en) * | 1951-01-09 | 1954-06-22 | Int Nickel Co | Mold and mold composition |
| US4608088A (en) * | 1984-03-22 | 1986-08-26 | Dento-Med Industries Incorporated | Denture adherent powder |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2249694A (en) * | 1938-09-26 | 1941-07-15 | Amalgamated Dental Co | Material for taking impressions for dental or other purposes |
| US2298835A (en) * | 1941-11-07 | 1942-10-13 | Stanley E Noyes | Dental impression composition |
| US2325051A (en) * | 1940-05-31 | 1943-07-27 | White S Dental Mfg Co | Dental impression compound |
-
1945
- 1945-04-30 US US591221A patent/US2425118A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2249694A (en) * | 1938-09-26 | 1941-07-15 | Amalgamated Dental Co | Material for taking impressions for dental or other purposes |
| US2325051A (en) * | 1940-05-31 | 1943-07-27 | White S Dental Mfg Co | Dental impression compound |
| US2298835A (en) * | 1941-11-07 | 1942-10-13 | Stanley E Noyes | Dental impression composition |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2568752A (en) * | 1947-07-28 | 1951-09-25 | Dental Perfection Company | Dental impression composition |
| US2681860A (en) * | 1951-01-09 | 1954-06-22 | Int Nickel Co | Mold and mold composition |
| US2678280A (en) * | 1952-03-21 | 1954-05-11 | Dental Perfection Company | Gel point indicating impression materials |
| US4608088A (en) * | 1984-03-22 | 1986-08-26 | Dento-Med Industries Incorporated | Denture adherent powder |
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