GB819779A - Improvements in method of making a fungicidal substance - Google Patents
Improvements in method of making a fungicidal substanceInfo
- Publication number
- GB819779A GB819779A GB39861/57A GB3986157A GB819779A GB 819779 A GB819779 A GB 819779A GB 39861/57 A GB39861/57 A GB 39861/57A GB 3986157 A GB3986157 A GB 3986157A GB 819779 A GB819779 A GB 819779A
- Authority
- GB
- United Kingdom
- Prior art keywords
- parts
- product
- fungicidal
- hours
- nabam
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/30—Dithiocarbamic acids; Derivatives thereof having sulfur atoms of dithiocarbamic groups bound to other sulfur atoms
- C07C333/32—Thiuramsulfides; Thiurampolysulfides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A fungicidal product believed to be a poly(ethylene bis-thiuram disulphide) is prepared by mixing disodium ethylene bis-dithiocarbamate (nabam), water or a volatile organic solvent liquid medium (e.g. benzene, n-hexane, CHCl3, petroleum ether or ligroin), and phosgene, at a temperature of from -10 DEG to 20 DEG C. for a period of from 1 to 20 hours, separating the resulting solid material and allowing the latter to evolve carbon oxysulphide spontaneously to leave a yellow fungicidal product. In an example, 52 parts (0.2 mol.) of anhydrous nabam were added to 500 parts of dry benzene and the mixture was cooled to 60 DEG C.; liquid phosgene (22 parts; 0.22 mol.) was added with stirring and the temperature was maintained at 7 DEG C. for 8 hours. After filtering and air drying, about 67 parts of material was obtained; this was washed to remove sodium chloride and the remaining solid was filtered and air dried, giving approximately 36 parts of a dull, white compound (m.p. 112 DEG C. with decomposition) which on standing for 36 hours at room temperature split off carbon oxysulphide to yield 23 parts (64 per cent yield) of an odourless, light yellow product, which softened and decomposed at about 132-135 DEG C. and had the X-ray diffraction pattern shown in Specification 816,341. The product is insoluble in water, soluble with decomposition in pyridine and alkaline aqueous alcohol or acetone, and partially soluble in acetone. It may be mixed with clay and wetting agents to form a fungicidal wettable powder.ALSO:A fungicidal composition is obtained by mixing nabam, water or a volatile organic solvent liquid medium, and phosgene at a temperature of - 10 DEG to 20 DEG C. for a period of an hour to 20 hours, separating the resulting solid material which is allowed to evolve carbon oxysulphide spontaneously to yield a yellow fungicidal product. Wetting agents and clay may be incorporated with the product. Specification 816,341 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US819779XA | 1957-01-28 | 1957-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB819779A true GB819779A (en) | 1959-09-09 |
Family
ID=22167613
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB39861/57A Expired GB819779A (en) | 1957-01-28 | 1957-12-23 | Improvements in method of making a fungicidal substance |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB819779A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1165578B (en) * | 1959-12-22 | 1964-03-19 | Schering Ag | Process for the preparation of thiuram disulfides |
-
1957
- 1957-12-23 GB GB39861/57A patent/GB819779A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1165578B (en) * | 1959-12-22 | 1964-03-19 | Schering Ag | Process for the preparation of thiuram disulfides |
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