223220
Thiocarbohydrazide
98%
Synonym(s):
Thiocarbonyldihydrazide
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(NH2NH)2CS
CAS Number:
Molecular Weight:
106.15
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39093513
UNSPSC Code:
12352100
EC Number:
218-769-8
MDL number:
Beilstein/REAXYS Number:
506657
Product Name
Thiocarbohydrazide, 98%
InChI key
LJTFFORYSFGNCT-UHFFFAOYSA-N
InChI
1S/CH6N4S/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)
SMILES string
NNC(=S)NN
assay
98%
form
solid
mp
171-174 °C (dec.) (lit.)
functional group
amine
hydrazine
thiourea
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
- Review of transition metal complexes with thiocarbohydrazides: This comprehensive review discusses the coordination chemistry of thiocarbohydrazides with various metals, highlighting their relevance in the synthesis of complex metal compounds used in catalysis and pharmaceutical research (Aly et al., 2023).
- Pd-doped nanocomposites for organometallic catalysis: Thiocarbohydrazide was employed in the fabrication of Pd-doped SBA-15 nanocomposites, applied as catalysts in the synthesis of organometallic compounds, showcasing its utility as a catalyst support material (Kalhor and Dadras, 2021).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Oral
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Kamaleddin Haj Mohammad Ebrahim Tehrani et al.
Iranian journal of pharmaceutical research : IJPR, 12(2), 331-346 (2013-11-20)
In this work, we reported the synthesis and evaluation of antimycobacterial and antifungal activity of a series of thiocarbohydrazone derivatives which are thiacetazone congeners. The target compounds were synthesized in superior yields by reacting thiocarbohydrazide with different aromatic aldehydes and
O Fujimori et al.
The Histochemical journal, 23(2), 91-99 (1991-02-01)
A method has been developed for the histochemical demonstration of unsaturated lipids in light microscopy. It is a peracetic acid-thiocarbohydrazide-silver protein sequence followed by a physical development procedure. In the present study on paraffin and cryostat sections of liver, brain
K S Siddiqi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(3-4), 995-1002 (2006-11-07)
Sn(tch)2{MCl2}2 was prepared from the precursor Sn(tch)2 and MCl2. It was subsequently allowed to react with diethyldithiocarbamate which yielded the trinuclear complexes of the type Sn(tch)2{M2(dtc)4}, where tch=thiocarbohydrazide, M=Mn(II), Fe(II), Co(II), Ni(II), Cu(II) and dtc=diethyldithiocarbamate. They were characterized on the
Anand D Tiwari et al.
International journal of biological macromolecules, 48(4), 682-687 (2011-02-26)
Chitosan-N-2-methylhydroxypyridine-6-methylcorboxylate (Ch-PDC) and chitosan-N-2-methylhydroxypyridine-6-methylhydroxy thiocarbohydrazide (Ch-PDC-Th) were synthesized for the first time using chitosan as precursor. Chitosan, Ch-PDC, Ch-PDC-Th were used in the synthesis of gold nanoparticles (AuNP) in aqueous medium. Chitosan and Ch-PDC-Th possess reducing properties which enabled the
M J Mourik et al.
Journal of microscopy, 259(2), 97-104 (2015-02-04)
Electron microscopy is used in biological research to study the ultrastructure at high resolution to obtain information on specific cellular processes. Serial block face-scanning electron microscopy is a relatively novel electron microscopy imaging technique that allows three-dimensional characterization of the
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service