USRE20718E - Chemical compound - Google Patents
Chemical compound Download PDFInfo
- Publication number
- USRE20718E USRE20718E US20718DE USRE20718E US RE20718 E USRE20718 E US RE20718E US 20718D E US20718D E US 20718DE US RE20718 E USRE20718 E US RE20718E
- Authority
- US
- United States
- Prior art keywords
- lead
- ortho
- cresol
- dinitro
- cresylate
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B41/00—Compositions containing a nitrated metallo-organic compound
- C06B41/02—Compositions containing a nitrated metallo-organic compound the compound containing lead
Definitions
- This invention relates to certain new chemical compounds of a somewhat explosive nature, to the preparation of such compounds, and to their use either alone or in conJunction with other substances as explosive compositions, particularly as compositions for use mixtures.
- the compounds are derivatives of ortho cresol. Confusion exists as to the naming of the derivaas ammunition primina' i0 tives of ortho cresol, due to the fact that the benzene ring contains two substitutions, one a methyl substitution and the other a hydroxyl substitution.
- the cresols may be considered as derived either from phenol or from toluene.
- the mono-basic lead salt is prepared as follows: A solution of 1.98 grams of 3-5 dinitroortho-cresol and .8 gram of sodium hydroxide in. 100 c. c. of water is dropped into asolution of 3.5
- the dl-basic lead salt is prepared as follows: A solution of 1.98 grams of 3-5 dinitro-orthocresol and 1.2 grams of sodium hydroxide in 100 c. c. of water is dropped slowly into'a solution of 10.5 grams of lead nitrate in 100 c. c. of water, at a temperature between 80 and C. After cooling, the precipitate is filtered oil, washed and dried. Said precipitate is in the form of brownish rhombic crystals. It will be noted that the quantity of lead nitrate is an excess of about over the theoretically re-acting quantity. It is necessary to use such an excess of lead nitrate in order to secure a crystalline precipitate.
- Typical priming mixtures are included in the following table:
- a priming composition containing a lead salt or 3-5 di-nitro ortho cresol, a suitable combustion initiator, and a suitable oxidizer.
- a priming composition containing di-basic lead 3-5 di-nitro ortho cresylate, a suitable combustion initiator, and a suitable oxidizer.
- the method of making mono-basic lead 3-5 dinitro ortho cresylate which comprises precipitating said salt by the addition to a solution of 35 grams of lead nitrate in 100 c. c. of water of a solution of 1.98 grams 'of 3-5 di-nitro ortho cresol and .8 gram of sodium hydroxide in 100 c. c. of water at a temperaturebetween '70 and 13.
- the method oi making di-basic lead 3-5 dinitro ortho cresylate which comprises precipitating said salt by the addition to a solution of 10.5 grams of lead nitrate in 100 c. c. 01 water of a solution of 1.98 grams of 3-5 di-nitro ortho cresoi and 1.2 grams of sodium hydroxide in 100 c. c. of water at a temperature between 80 and 90 C.
Description
so the term "cresol" Reiaued May 10, 1938 UNITED STATES PATENT oar-ice CHEMICAL COMPOUND Willi Briin, Bridgeport, Com, assilnor to Remington ware No Drawing.
l'll'inal an 18, 1984, Serial No- 569,838,
Arms Company, Ina, a corporation of No. 1,943,513, dated Janu-- October 19,
1931. Application for reissue July 21, 1937, Se-
rial No. 154,806
13 Claims.
This invention relates to certain new chemical compounds of a somewhat explosive nature, to the preparation of such compounds, and to their use either alone or in conJunction with other substances as explosive compositions, particularly as compositions for use mixtures.
The compounds are derivatives of ortho cresol. Confusion exists as to the naming of the derivaas ammunition primina' i0 tives of ortho cresol, due to the fact that the benzene ring contains two substitutions, one a methyl substitution and the other a hydroxyl substitution. The cresols may be considered as derived either from phenol or from toluene. In
15 identifying the derivatives of ortho cresol, such as those containing nitro substitution groups, these groups may be located either from the methyl group or from the OH group. Beilstein (vol. VI) gives alternative nomenclature, using when and only when the position ,of the hydroxy group is considered as 1" position. Other literature and commercial practice has not always followed Beilstelns nomenclature. In recognition of the existing confusion g5 Beilstein's 1931 supplement takes the extraordinary precaution of including structural formulas in the text. The cresol derivative which is utilized by the applicant in the present invention contains two separated nitro groups and is the onlyknown dinitro-ortho-cresol inwhich the nitro groups are separated. It isidentified by commercial suppliers as "3-5 dinitro-ortho-cresol", and
is identical with the-compound which Beilstein identifies as "4-6 dinitro-ortho-cresol". For the as purpose of this specification, the commercial identification will be used, it beingunderstood that the compound is also known as "4-6 dinitroortho-cresol.
By the addition, under suitable conditions, of
40 lead nitrate solutions to solutions of 3-5 dinitro ortho cresol, two new compositions of matter have been made which are indicated by analysis to be, respectively, mono-basic lead 3-5 dinitro cresylate and di-basic lead 3-5 dinitro cresylate,
48 and in this specification will be so identified.
The mono-basic lead salt is prepared as follows: A solution of 1.98 grams of 3-5 dinitroortho-cresol and .8 gram of sodium hydroxide in. 100 c. c. of water is dropped into asolution of 3.5
grams of lead nitrate in 100 c. c. of water, at a temperature between and C. The precipitate, which is of a light yellow color and of fluffy character, is filtered 01! and washed with water. It has a lead content of 48.84%, corre- Bl sponding substantially to the theoretical lead content, 49.19%, of mono-basic lead 8-5 dinitroortho-cresylate.
The dl-basic lead salt is prepared as follows: A solution of 1.98 grams of 3-5 dinitro-orthocresol and 1.2 grams of sodium hydroxide in 100 c. c. of water is dropped slowly into'a solution of 10.5 grams of lead nitrate in 100 c. c. of water, at a temperature between 80 and C. After cooling, the precipitate is filtered oil, washed and dried. Said precipitate is in the form of brownish rhombic crystals. It will be noted that the quantity of lead nitrate is an excess of about over the theoretically re-acting quantity. It is necessary to use such an excess of lead nitrate in order to secure a crystalline precipitate. The use of the theoretical quantity results in an amorphous yellow precipitate only. The precipitated compound is found upon analysis to have a lead content of 57.35% which is almost identical with the theoretical lead content, 57.36%, of dl-basic lead 3-5 dinitro-ortho-cresylate.
Both of these salts have been found useful as priming mixture ingredients, particularly priming mixture fuels. The di-basic salt, however, is preferred for this purpose on. account of its greater density and crystalline character. The semi-explosive character of either salt addsto its value as a priming mixture fuel, since mixtures containing such semi-explosive fuels tend to be more sensitive to percussion than mixtures utilizing only inert substances as fuels.
Typical priming mixtures are included in the following table:
' Per cent Mercury fulminate 30 to 50 Barium nitrate 20 to 40 Mono-basic or di-basic lead 3-5 dinitroortho-cresylate 5 to 15 Abrasive -substantially 20 This formula, however, is merely typical. The
explosive, mercury fulrnlnate,-may be replaced The said lead salts being themselves novel, the appended claims are to be broadly construed.
What is claimed is: 1. As a composition of matter, a lead salt of 3-5 di-nitro ortho cresol.
2. As a composition of matter, a basic lead salt of 3-5 dinitro ortho cresol.
3, As a composition or matter, mono-basic lead 3-5 di-nitro ortho cresylate.
4. As a composition of matter, di-basic lead 3-5 di-nitro ortho cresylate.
5. A priming composition containing a lead salt of 3-5 dinitro ortho cresol.,
6. A priming composition containing a basic lead salt of 3-5 dinitro ortho cresol.
7. A priming composition containing monobasic lead 3-5 di-nitro ortho cresylate.
B. A priming composition containing di-basic lead 3-5 di-nitro ortho'cresylate.
9. A priming composition containing a lead salt or 3-5 di-nitro ortho cresol, a suitable combustion initiator, and a suitable oxidizer. v
10. A priming composition containing di-basic lead 3-5 di-nitro ortho cresylate, a suitable combustion initiator, and a suitable oxidizer.
11.. The method of making a lead salt of 3-5 dinitro ortho cresol which comprises the addition to an aqueous solution of lead nitrate of an aqueous solution or sodium hydroxide and 3-5 di-nitro ortho cresol.
12. The method of making mono-basic lead 3-5 dinitro ortho cresylate, which comprises precipitating said salt by the addition to a solution of 35 grams of lead nitrate in 100 c. c. of water of a solution of 1.98 grams 'of 3-5 di-nitro ortho cresol and .8 gram of sodium hydroxide in 100 c. c. of water at a temperaturebetween '70 and 13. The method oi making di-basic lead 3-5 dinitro ortho cresylate, which comprises precipitating said salt by the addition to a solution of 10.5 grams of lead nitrate in 100 c. c. 01 water of a solution of 1.98 grams of 3-5 di-nitro ortho cresoi and 1.2 grams of sodium hydroxide in 100 c. c. of water at a temperature between 80 and 90 C.
. WILLI 1mm.
Publications (1)
Publication Number | Publication Date |
---|---|
USRE20718E true USRE20718E (en) | 1938-05-10 |
Family
ID=2085889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US20718D Expired USRE20718E (en) | Chemical compound |
Country Status (1)
Country | Link |
---|---|
US (1) | USRE20718E (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2922804A (en) * | 1956-11-23 | 1960-01-26 | Gen Electric | Basic lead p-nitrosophenolate |
-
0
- US US20718D patent/USRE20718E/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2922804A (en) * | 1956-11-23 | 1960-01-26 | Gen Electric | Basic lead p-nitrosophenolate |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Wasson et al. | Effect of alkyl substitution on antioxidant properties of phenols | |
USRE23024E (en) | X-dimethylaminophenyl | |
Hunter et al. | 145. The associating effect of the hydrogen atom. Part IX. The N–H–N bond. Virtual tautomerism of the formazyl compounds | |
USRE20718E (en) | Chemical compound | |
US2192197A (en) | Dinitro-alkyl-phenol | |
US2148705A (en) | Azo compounds | |
US2387751A (en) | N-aryltetrahydroquinolines | |
US2112244A (en) | Amino azobenzene arsonic acids | |
US2294723A (en) | Stabilized dry rosin size | |
US1708187A (en) | Combustible composition | |
Pollecoff et al. | LV.—Nitro-derivatives of guaiacol | |
Haworth et al. | 76. Nitrosoacylarylamines. Part II. The action of nitrous fumes on acylarylamines | |
US1942274A (en) | Priming mixture | |
US1943513A (en) | Chemical compound | |
US2702745A (en) | Styphnate compound and priming composition thereof | |
US2205116A (en) | Explosive | |
US3098847A (en) | Disazo dyes | |
Heidelberger et al. | SYNTHESES IN THE CINCHONA SERIES. III. AZO DYES DERIVED FROM HYDROCUPREINE AND HYDROCUPREIDINE. | |
US1991730A (en) | Lead salt of dinitro benzoic acid and priming composition containing the same | |
US2502708A (en) | Nitro-hydrogenated cardanols and process for preparing same | |
US2728760A (en) | Reaction product of hydrazine and its derivatives with diazophenol and its derivatives, and salts of such products | |
US2294727A (en) | Stabilized dry rosin size | |
US2084033A (en) | Dichlorohydroxydiphenyl | |
Browning et al. | Therapeutic interference caused by isomerides of trypanocidal styryl quinoline derivatives | |
Pratt et al. | CCLVIII.—A synthesis of pyrylium salts of anthocyanidin type. Part XII |