11.
    发明专利
    未知

    公开(公告)号:SE341629B

    公开(公告)日:1972-01-10

    申请号:SE1741367

    申请日:1967-12-19

    Abstract: 1,132,297. Methylene bisesters of thiosulphonic acids. BUCKMAN LABORATORIES Inc. 13 Oct., 1967 [12 May, 1967], No. 46886/67. Heading C2C. [Also in Divisions A5, C6 and D2] Novel methylene bisesters of thiosulphonic acids of the general formula wherein R and R 1 each represents a straight or branched chain C 1 -C 6 alkyl, alicyclic or aryl group, or a substituted aryl group wherein 1-3 of the hydrogen atoms are replaced by alkyl, hydroxy, nitro, or halogen, the substituents attached to the aryl group being the same or different, are prepared by reacting an alkali metal salt of a thiosulphonic acid of formula RSO 2 SH and/or an alkali metal salt of a thiosulphonic acid of formula R 1 SO 2 SH with methylene bromide or methylene iodide.

    15.
    发明专利
    未知

    公开(公告)号:FI47528B

    公开(公告)日:1973-10-01

    申请号:FI120368

    申请日:1968-04-26

    Abstract: 1,168,744. Microbiocidal treatment BUCKMAN LABORATORIES Inc. 18 June, 1968 [8 March, 1968], No. 29059/68. Headings A2D and A2Q. [Also in Divisions A5, C2, C6, D2 and E1] A microbiocidal composition comprises an organic thiocyanate and a 2-hydroxyalkyl ester of an organic thiolsulphonic acid. Typical compounds used are 2-(thiocyanomethylthio) benzothiazole, benzoxazole or benzimidazole, or methylene bisthoscyanate; and 2-hydroxyethyl or 2-hydroxypropyl methanethiolsulphonate. The composition may be applied to substances which contain or are contacted with water, e.g. seeds, fruit, vegetables, berries, flowers, tobacco, cereals, starch, hides, tanning liquors and leather. '

    16.
    发明专利
    未知

    公开(公告)号:NO118715B

    公开(公告)日:1970-02-02

    申请号:NO188168

    申请日:1968-05-14

    Abstract: 1,168,744. Microbiocidal treatment BUCKMAN LABORATORIES Inc. 18 June, 1968 [8 March, 1968], No. 29059/68. Headings A2D and A2Q. [Also in Divisions A5, C2, C6, D2 and E1] A microbiocidal composition comprises an organic thiocyanate and a 2-hydroxyalkyl ester of an organic thiolsulphonic acid. Typical compounds used are 2-(thiocyanomethylthio) benzothiazole, benzoxazole or benzimidazole, or methylene bisthoscyanate; and 2-hydroxyethyl or 2-hydroxypropyl methanethiolsulphonate. The composition may be applied to substances which contain or are contacted with water, e.g. seeds, fruit, vegetables, berries, flowers, tobacco, cereals, starch, hides, tanning liquors and leather. '

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