GB487804A - Process for rendering materials mothproof - Google Patents
Process for rendering materials mothproofInfo
- Publication number
- GB487804A GB487804A GB6596/37A GB659637A GB487804A GB 487804 A GB487804 A GB 487804A GB 6596/37 A GB6596/37 A GB 6596/37A GB 659637 A GB659637 A GB 659637A GB 487804 A GB487804 A GB 487804A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- sulphonium
- prepared
- dimethyl
- methosulphate
- 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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
- A01N33/10—Amines; Quaternary ammonium compounds containing oxygen or sulfur having at least one oxygen or sulfur atom directly attached to an aromatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Textiles, fur, and feathers are rendered moth-proof by treatment with a sulphonium compound of the formula <FORM:0487804/IV/1> in which X represents the radical of an inorganic acid or an organic sulpho or carboxyl compound, and R1, R2, R3 represent the same or different substituted or unsubstituted aromatic residues, or one of these may alternatively stand for a lower alkyl radical. The cyclic residues may be substituted by basic, acid or neutral substituents, such as NH2, NH.alkyl, N(alkyl)2, OH, O.alkyl, COOH, halogen, or alkyl. Two o the aryl residues may also be linked to one another, in ortho-positions to the S-atom, by S, O, CO, or NR (where R is an aliphatic or araliphatic residue). The compounds may be used in solution in water, an alcohol, a ketone, a hydrocarbon or other organic solvent and may be applied by brushing, spraying or immersion, or may be precipitated from alkaline solution by addition of an acid. The solutions are stated to have strong wetting action. When aqueous solutions are used they may contain also Glauber's salt. Examples of active compounds are triphenyl sulphonium chloride, tripara-oxy-triphenyl sulphonium chloride, S-phenyl-thianthrene-sulphonium chloride (prepared by condensing thianthrene-S-oxide in excess benzene in presence of aluminium chloride), 2 : 6-dimethyl-S-methyl-thianthrene sulphonium methosulphate (prepared by treating 2 : 6-dimethyl-thianthrene with dimethyl sulphate), 2 : 7-dichlor-S-methyl-thianthrene sulphonium methosulphate (prepared by treating 2 : 7-dichlorothianthrene with dimethyl sulphate), N - methyl - S - phenyl - diphenylamine sulphonium chloride (prepared by condensing N-methyl-S-oxy-thio-diphenylamine with benzene in presence of aluminium chloride), 3 : 6-dimethyl-N-methyl-S-methyl-diphenylamine-sulphonium methosulphate (prepared by treating 3 : 6-dimethyl-N-methyl-thio diphenylamine with dimethyl sulphate), 4-methyl-6-oxy-N.methyl-3-methyl-diphenylamine-sulphonium methosulphate (prepared by treating 4-methyl-6 - oxy - N - methyl - thio - diphenylamine with dimethyl sulphate), S - phenyl - di - ortho - phenylene - oxide - sulphonium chloride (prepared by condensing phenoxthine-S-oxide with benzene in presence of aluminium chloride) 3 : 6-dimethyl-S-methyl-ortho-phenylene-oxide-sulphonium methosulphate (prepared by treating 3 : 6-dimethyl-phenoxthine with dimethyl sulphate), 3 : 6 - diamyl - S - methyl - ortho - phenylene - oxide - sulphonium methosulphate (prepared by treating 3 : 6 - diamylphenoxthine with dimethyl sulphate), 1 : 3-dichloro - 6 - methyl - S - methyl - orthophenylene-oxide-sulphonium methosulphate (prepared by treating 1 : 3 dichloro - 6 - methylphenoxthine with dimethylsulphate) and S-methyl-thioxanthrone-sulphonium methosulphate (prepared by treating thioxanthone with dimethyl sulphate).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE487804X | 1936-03-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB487804A true GB487804A (en) | 1938-06-27 |
Family
ID=6543695
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6596/37A Expired GB487804A (en) | 1936-03-14 | 1937-03-05 | Process for rendering materials mothproof |
Country Status (3)
Country | Link |
---|---|
FR (1) | FR818994A (en) |
GB (1) | GB487804A (en) |
NL (1) | NL51368C (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3402248A (en) * | 1965-06-28 | 1968-09-17 | Monsanto Co | Method of controlling fungi with sulfonium iodides |
-
0
- NL NL51368D patent/NL51368C/xx active
-
1937
- 1937-03-05 GB GB6596/37A patent/GB487804A/en not_active Expired
- 1937-03-10 FR FR818994D patent/FR818994A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR818994A (en) | 1937-10-07 |
NL51368C (en) |
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