4-Methyl-3-thiosemicarbazide - ≥96% , CAS No.6610-29-3

CAS: 6610-29-3 Cat. No.: M101900 Peso molecular: 105.16 Beilstein Registry Number: 4,72 Número EC: 229-563-2
Disponible para pedir
GRADE & PURITY ≥96%
Synonyms
4-N-METHYLTHIOSEMICARBAZIDE | EINECS 229-563-2 | Methylthiosemicarbazide | 3-amino-1-methylthiourea | SCHEMBL8126729 | D77757 | Hydrazinecarbothioamide, N-methyl- | 4methylthiosemicarbazide | 4-Methylthiosemicarbazide | 4-methyl-thiosemicarbazide | N-meth
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
M101900-5g
1
51,90US$
25g
M101900-25g
3
179,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Description

4-Methyl-3-thiosemicarbazide is a subject of considerable pharmacological interest owing to its wide range of biological effects. 


Product Application

4-Methyl-3-thiosemicarbazide was used in the analysis of electronic features of sulfur-using, high-resolution, low-temperature X-ray diffraction datasets.4-Methyl-3-thiosemicarbazide was used in the analysis of electronic features of sulfur-using, high-resolution, low-temperature X-ray diffraction datasets.

Specifications

Sinónimos
4-N-METHYLTHIOSEMICARBAZIDE | EINECS 229-563-2 | Methylthiosemicarbazide | 3-amino-1-methylthiourea | SCHEMBL8126729 | D77757 | Hydrazinecarbothioamide, N-methyl- | 4methylthiosemicarbazide | 4-Methylthiosemicarbazide | 4-methyl-thiosemicarbazide | N-meth
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥96%
Nombres e identificadores
Sonrisas canónicasCNC(=S)NN
IUPAC Name1-amino-3-methylthiourea
InChIKeyPTVZQOAHCSKAAS-UHFFFAOYSA-N
INCHI1S/C2H7N3S/c1-4-2(6)5-3/h3H2,1H3,(H2,4,5,6)
Isómeros SMILES CNC(=S)NN
WGK Alemania 3
RTECS MV1407370
Número ONU 2811
Peso molecular 105.16
Beilstein 4,72
Reaxy-Rn 605575
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605575&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClaseOrganonitrogen compounds
SubclassHydrazines and derivatives
Intermediate Tree Nodes Not available
Direct ParentThiosemicarbazides
Alternative Parents Organosulfur compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Thiosemicarbazide - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeFechaArticulo
F2419421Certificate of AnalysisApr 11, 2024 M101900
F2419446Certificate of AnalysisApr 11, 2024 M101900
F2419447Certificate of AnalysisApr 11, 2024 M101900
F2419448Certificate of AnalysisApr 11, 2024 M101900
F2220378Certificate of AnalysisJun 22, 2022 M101900
F2220379Certificate of AnalysisJun 22, 2022 M101900
F2220335Certificate of AnalysisJun 21, 2022 M101900
F2220377Certificate of AnalysisJun 21, 2022 M101900
Propiedades químicas y físicas
SolubilidadSoluble in alcohol. Slightly soluble in water.
Punto de fusión (°C)135-138°C
Peso molecular105.170 g/mol
XLogP3-0.800
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass105.036 Da
Monoisotopic Mass105.036 Da
Topological Polar Surface Area82.200 Ų
Heavy Atom Count6
Formal Charge0
Complexity52.800
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Xiaoyan Zhao, Shirong Kang, Hao Zhang, Hua Yang, Mingyu Dou, Haitao Zhao, Dacheng Li, Jianmin Dou.  (2023)  Highly efficient binuclear cobalt-bis(4-methylthiosemicarbazone) complex co-catalyst to support Cd0.5Zn0.5S NPs for enhanced photocatalytic hydrogen evolution.  INORGANICA CHIMICA ACTA,      [PMID:] [10.1016/j.ica.2023.121497]
2. Hao Zhang, Hongjie Zhu, Haitao Zhao, Mingyu Dou, Xingliang Yin, Hua Yang, Dacheng Li, Jianmin Dou.  (2022)  A novel dinuclear cobalt-bis(thiosemicarbazone) complex as a cocatalyst to enhance visible-light-driven H2 evolution on CdS nanorods and a mechanism discussion.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2022.113771]
3. Peifang Wang, Yue Su, Min Ma, Yuqing Wang, Shuang Hou, Changqing Wang, Lin Sun, Jianshe Wei, Mingxue Li.  (2024)  Thiosemicarbazones-Loaded Injectable Hydrogels with Self-Healing and Antibacterial Activity for Wound Healing.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c00994]
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