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accelerator tmtm etramethylthiuram monosulfide cas 97-74-5
accelerator tmtm etramethylthiuram monosulfide cas 97-74-5
accelerator tmtm etramethylthiuram monosulfide cas 97-74-5
accelerator tmtm etramethylthiuram monosulfide cas 97-74-5
accelerator tmtm etramethylthiuram monosulfide cas 97-74-5
  • What is the physiologic effect of tetramethylthiuram monosulfide?
  • The physiologic effect of tetramethylthiuram monosulfide is by means of Increased Histamine Release, and Cell-mediated Immunity. dimethylcarbamothioyl N, N -dimethylcarbamodithioate Computed by Lexichem TK 2.7.0 (PubChem release 2025.04.14) InChI=1S/C6H12N2S3/c1-7 (2)5 (9)11-6 (10)8 (3)4/h1-4H3 Computed by InChI 1.07.2 (PubChem release 2025.04.14)
  • Does tetramethylthiuram monosulfide have an individual approval?
  • Tetramethylthiuram monosulfide: Does not have an individual approval but may be used under an appropriate group standard
  • Does tetramethylthiuram monosulfide inhibit ADH?
  • The dimers thiram (TMTD), disulfiram (TETD), and tetramethylthiuram monosulfide (TMTM) inhibited ADH more than the metal containing dithiocarbamates zineb and maneb or the monomer salts dimethyldithiocarbamate (DMDC), diethyldithiocarbamate (DEDC) and ziram using either ethanol or NAD as the main substrate.
  • Is tetramethylthiuram disulfide biodegraded?
  • A similar compound, the disulfide (tetramethylthiuram disulfide), was biodegraded in six soils during a study using an enriched culture with a maximum degradation of 88.5% after 24 days in peat, followed by black soil (86.5%), laterite (78.86%), alluvial (75%), and red soil (57.85%) (2).
  • Does tetramethylthiuram monosulfide prolong hexobarbital sleeping time in wistar rats?
  • Tetramethylthiuram monosulfide (TMTM) when given in a small dose of 26 mg/kg orally caused prolongation of the hexobarbital sleeping time in female Wistar rats. This effect was enhanced by increasing the dose to 867 mg/kg orally and was associated with a lengthening of the zoxazolamine paralysis time.
  • What is the LD50 of TmTm?
  • In female mice given acute oral doses of TMTM, the LD50 was calculated as 818 (583-995) mg/kg. In mutagenicity tests, TMTM caused point mutations in strains TA 100 and TA 1535 (Salmonella typhimurium LT 2).
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