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About This Item
Empirical Formula (Hill Notation):
C10H8N2S2
CAS Number:
Molecular Weight:
220.31
UNSPSC Code:
12352112
NACRES:
NA.25
PubChem Substance ID:
EC Number:
218-343-1
Beilstein/REAXYS Number:
154629
MDL number:
Quality Level
assay
≥99.0% (GC)
form
solid
mp
56-58 °C (lit.), 57-59 °C
storage temp.
2-8°C
SMILES string
S(Sc1ccccn1)c2ccccn2
InChI
1S/C10H8N2S2/c1-3-7-11-9(5-1)13-14-10-6-2-4-8-12-10/h1-8H
InChI key
HAXFWIACAGNFHA-UHFFFAOYSA-N
Other Notes
For the determination of sulfhydryl groups in biological materials
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Determination of sulfhydryl groups with 2,2'- or 4,4'-dithiodipyridine.
D R Grassetti et al.
Archives of biochemistry and biophysics, 119(1), 41-49 (1967-03-01)
Rachel Lubong Sabado et al.
PloS one, 4(1), e4256-e4256 (2009-01-24)
The requirements for priming of HIV-specific T cell responses initially seen in infected individuals remain to be defined. Activation of T cell responses in lymph nodes requires cell-cell contact between T cells and DCs, which can give concurrent activation of
Sanae Haga et al.
Antioxidants & redox signaling, 11(10), 2563-2572 (2009-06-06)
Noninvasive evaluation of organ redox states provides invaluable information in many clinical settings. We evaluated a newly developed reduction/oxidation-sensitive green fluorescent protein (roGFP) probe that reports cellular redox potentials and their dynamic changes in live cells. On hypoxia/reoxygenation (H/R) of
