Ordering
Available Variants1 g
CHA.51392-1g
Price
€30.48
Available – Dispatch in 14 days
5 g
CHA.51392-5g
Price
€104.80
Available – Dispatch in 14 days
25 g
CHA.51392-25g
Price
€384.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.51392-1g | €30.48 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.51392-5g | €104.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.51392-25g | €384.80 |
powder
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C10H8N2S2 |
|---|---|
| CAS Number | 2127-03-9 |
| Molecular Weight | 220.31 |
| UNSPSC Code | 12352112 |
| NACRES | NA.26 |
| PubChem Substance ID | 24893969 |
| EC Number | 218-343-1 |
| Beilstein/REAXYS Number | 154629 |
| MDL number | MFCD00006287 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| 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 |
Technical Overview & Applications Use-case context
2,2′-Dithiodipyridine, with a CAS number of 2127-03-9, is a chemical compound consisting of two pyridine rings connected by a disulfide bond. This compound has been utilized in various applications, including as a precursor for the synthesis of other molecules and as a ligand in coordination chemistry. The disulfide bond in 2,2′-Dithiodipyridine can be cleaved to form thiopyridine derivatives, which have been employed in the preparation of pharmaceuticals and materials. Additionally, 2,2′-Dithiodipyridine has been used as a building block in the construction of supramolecular assemblies and as a reagent in organic synthesis reactions. Its unique structure and reactivity make it a valuable compound in various fields of chemistry, and its properties continue to be explored and utilized in ongoing research efforts. Further studies on this compound are expected to reveal new applications and uses.
