4-Methyl-3-thiosemicarbazide

4-Methyl-3-thiosemicarbazide
Names
Preferred IUPAC name
N-Methylhydrazinecarbothioamide
Identifiers
CAS Number
  • 6610-29-3
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL3182946
ChemSpider
  • 2006040 checkY
ECHA InfoCard 100.026.876 Edit this at Wikidata
EC Number
  • 229-563-2
PubChem CID
  • 2723853
UNII
  • PK83E1T776
CompTox Dashboard (EPA)
  • DTXSID7044390
InChI
  • InChI=1S/C2H7N3S/c1-4-2(6)5-3/h3H2,1H3,(H2,4,5,6) checkY
    Key: PTVZQOAHCSKAAS-UHFFFAOYSA-N checkY
  • InChI=1S/C2H7N3S/c1-4-2(6)5-3/h3H2,1H3,(H2,4,5,6)
    Key: OKISUZLXOYGIFP-UHFFFAOYAC
  • CNC(=S)NN
Properties
Chemical formula
 C2H7N3S
Molar mass 105.16 g·mol−1
Melting point 135 to 138 °C (275 to 280 °F; 408 to 411 K)[1]
Hazards
GHS labelling:
Pictograms
 GHS06: Toxic
Danger
Hazard statements
 H300
Precautionary statements
 P264, P270, P301+P310, P321, P330, P405, P501
Lethal dose or concentration (LD, LC):
LD50 (median dose)
 14 mg/kg rat
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references
Chemical compound

4-Methyl-3-thiosemicarbazide is an organosulfur compound with the formula of CH3NHC(S)NHNH2. It is a white, odorless solid. The compound is one of the many derivatives of thiosemicarbazide. It is a precursor to diverse organic compounds and metal complexes.

Applications

4-Methyl-3-thiosemicarbazide is used as an intermediate compound in the synthesis of some types of herbicides, for example tebuthiuron.[2]

Structure of Ni(H2NNCSNHMe)2.[3]

Precautions and toxicity

4-Methyl-3-thiosemicarbazide can cause irritation of the eyes, respiratory tract, and skin. Swallowing the chemical may cause death.[1] It is classified as a "dangerous good for transport".[4]

References

  1. ^ a b Material Safety Data Sheet, October 26, 2012, retrieved August 23, 2013
  2. ^ Ralph Kenneth Achgill, Laurence Wesley Call (November 2, 1989), Improved synthesis of 4-methyl-3-thiosemicarbazide, retrieved August 24, 2013
  3. ^ Burrows, Andrew D.; Harrington, Ross W.; Mahon, Mary F.; Teat, Simon J. (2002). "Structural manipulation through selective substitution of hydrogen bonding groups: The supramolecular structures of bis(thiosemicarbazidato)nickel complexes". CrystEngComm. 4 (89): 539. doi:10.1039/b208284e.
  4. ^ 4-Methyl-3-thiosemicarbazide (CAS 6610-29-3), 2007, retrieved August 24, 2013


  • v
  • t
  • e