tetramethylthiuram monosulfide (tmtm) chemotechnique

  • tetramethylthiuram monosulfide (tmtm) | chemotechnique

    Tetramethylthiuram monosulfide (TMTM) | Chemotechnique

    Tetramethylthiuram monosulfide (TMTM) Print. Art.No T-006 Formula C 6 H 12 N 2 S 3. Conc Chemotechnique MB Diagnostics AB Modemgatan 9 | SE-235 39 | Vellinge | Sweden

  • tetramethylthiuram monosulfide (tmtm) - chemotechnique.se

    Tetramethylthiuram monosulfide (TMTM) - chemotechnique.se

    Tetramethylthiuram monosulfide (TMTM) (T-006) Your patch testing results indicate that you have a contact allergy to Tetramethylthiuram monosulfide (TMTM). It is important that you familiarize yourself with this chemical and take steps to avoid coming in contact with it. What is Tetramethylthiuram monosulfide (TMTM) and where is it found?

  • thiuram mix | chemotechnique diagnostics

    Thiuram mix | Chemotechnique Diagnostics

    Tetramethylthiuram monosulfide (TMTM) 0.25% pet Search database. Find: Products >> Chemotechnique MB Diagnostics AB Modemgatan 9 | SE-235 39 | Vellinge | Sweden Tel

  • tetramethylthiuram monosulfide | c6h12n2s3

    Tetramethylthiuram monosulfide | C6H12N2S3

    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. Both effects were causally related to an

  • tetramethylthiuram sulfide

    Tetramethylthiuram sulfide

    Tetramethylthiuram sulfide is an organosulfur compound with the formula ((CH 3) 2 NCS) 2 S. It is a yellow solid that is soluble in organic solvents. It is the parent member of a large class of tetraalkylthiuram sulfides.

  • tetramethylthiuram monosulfide 97%

    Tetramethylthiuram monosulfide 97%

    Tetramethylthiuram monosulfide 97% Synonym: UNADS CAS Number 97-74-5. Linear Formula ((H 3 C) 2 NCS) 2 S . Molecular Weight 208.37 . EC Number 202-605-7. MDL number MFCD00014870. PubChem Substance ID 24880353. NACRES NA.22

  • tetramethylthiuram monosulphide - registration dossier - echa

    Tetramethylthiuram monosulphide - Registration Dossier - ECHA

    The test item Tetramethylthiuram monosulfide was dissolved in dimethylsulfoxide (DMSO). Experiments without S9 mix : The selected treatment-levels for both mutagenicity experiments were: 156.3, 312.5, 625, 1250, 2500 and 5000 µg/plate.

  • tetramethylthiuram monosulfide (tmtm)

    TETRAMETHYLTHIURAM MONOSULFIDE (TMTM)

    Tetramethylthiuram monosulfide (TMTM) is used as a secondary accelerator with thiazoles, guanidines, sulfenamides and dithiocarbamates. It is used as a fungicide, and insecticide.

  • tetramethylthiuram monosulfide | ≥99%(hplc) | selleck

    Tetramethylthiuram monosulfide | ≥99%(HPLC) | Selleck

    Tetramethylthiuram monosulfide is used on a large scale as a catalyst in rubber-processing techniques. Tetramethylthiuram monosulfide possesses a medium-degree toxicity and causes point mutations in strains TA 100 and TA 1535 (Salmonella typhimurium LT 2).

  • tetramethylthiuram monosulfide - huidziekten

    Tetramethylthiuram monosulfide - huidziekten

    Tetramethylthiuram monosulfide is an accelerator and activator for natural rubber nitrile-butadiene, and butyl rubber. Synonyms. Tetramethylthiuram monosulfide TMTM . Uses. Adhesives Condoms and diaphragms Disinfectants, repellents, fungicides, and insecticides in agriculture DIsulfiram (Antabuse) Gloves (household, work, or hospital)

  • tetramethylthiuram monosulfide - hazardous agents | haz-map

    Tetramethylthiuram monosulfide - Hazardous Agents | Haz-Map

    Tetramethylthiuram monosulfide agent detailed information in Haz-Map database.

  • tetramethylthiuram monosulphide - registration dossier - echa

    Tetramethylthiuram monosulphide - Registration Dossier - ECHA

    Tetramethylthiuram monosulfide was readily degraded by light and its degradation products were shown to be as toxic as the parent compound. Therefore, additional flasks pre-exposed to light were also inoculated and incubated under the same conditions as the "fresh flask": the first test item stock solutions (at 20 mg/L nominal concentration