GRADE & PURITY ≥98%

Synonyms

3-amino-1,1-dimethylthiourea | EN300-73512 | A866877 | C3H9N3S | Hydrazinecarbothioamide,N,N-dimethyl- | NSC166599 | NSC-166599 | 4,4-Dimethyl-3-thiosemicarbazide | 4,4-Dimethyl-3-thiosemicarbazide, 98% | D2096 | AKOS005207228 | N,N-Dimethylhydrazinecarbo

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyms

3-amino-1, 1-dimethylthiourea | EN300-73512 | A866877 | C3H9N3S | Hydrazinecarbothioamide, N, N-dimethyl- | NSC166599 | NSC-166599 | 4, 4-Dimethyl-3-thiosemicarbazide | 4, 4-Dimethyl-3-thiosemicarbazide, 98% | D2096 | AKOS005207228 | N, N-Dimethylhydrazinecarbo

Specifications & Purity

≥98%

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504761026
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504761026
• Canonical Smiles: CN(C)C(=S)NN
• IUPAC Name: 3-amino-1,1-dimethylthiourea
• InChIKey: FCPHVJQWZFNNKD-UHFFFAOYSA-N
• INCHI: 1S/C3H9N3S/c1-6(2)3(7)5-4/h4H2,1-2H3,(H,5,7)
• Isomeric SMILES: CN(C)C(=S)NN
• WGK Germany: 3
• Molecular Weight: 119.19
• Reaxy-Rn: 1747186
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1747186&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Hydrazines and derivatives

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Hydrazines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Thiosemicarbazides
• Alternative Parents: Organosulfur compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Thiosemicarbazide - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as thiosemicarbazides. These are compounds containing a derivative of thiosemicarbazide with the general structure R1N(R2)N(R3)C(=S)N(R4)R5 (R1-R5=H, alkyl, aryl) where the ketone group has carbonyl group has been replaced with a thiocarbonyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Air Sensitive,Heat Sensitive
• Molecular Weight: 119.190 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 119.052 Da
• Monoisotopic Mass: 119.052 Da
• Topological Polar Surface Area: 73.400 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 70.600
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Dan Li, Minghui Fan, Haobing Wang, Yongjie Zhu, Bole Yu, Pingyu Zhang, Huaiyi Huang.  (2024)  Facile synthesis of a hydrazone-based zinc(II) complex for ferroptosis-augmented sonodynamic therapy.  Chemical Science,      [PMID:38966369] [10.1039/D4SC02102A]