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Chemodex
N-Succinimidyl 3-(2-pyridyldithio)propionate
Product Details | |
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Synonyms | 3-(2-Pyridyldithio)propionic acid N-hydroxysuccinimide ester; SPDP |
Product Type | Chemical |
Properties | |
Formula | C12H12N2O4S2 |
MW | 312.36 |
CAS | 68181-17-9 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥97% (NMR) |
Appearance | White to off-white powder. |
Solubility | Soluble in acetone (50mg/ml), DMF or methanol. |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | JWDFQMWEFLOOED-UHFFFAOYSA-N |
Smiles | O=C(CCSSC1=NC=CC=C1)ON2C(CCC2=O)=O |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +4°C |
Long Term Storage | -20°C |
Handling Advice | Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at -20°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
N-Succinimidyl 3-(2-pyridyldithio)propionate is a heterobifunctional cross-linking reagent with amine and sulfhydryl reactivity. It is typically coupled initially to molecules containing primary amines by amide bonds buffered at pH 7.5 (6.5-8.5). Second coupling specific for molecules containing free sulfhydryl by thiol-disulfide exchange buffered at pH 8.0 (7.5-8.5). Alternately, this reagent may be used as a protected thiolating reagent following initial coupling and reduction of linker. It incorporates four atom linker. N-Succinimidyl 3-(2-pyridyldithio)propionate (SPDP) is useful for the preparation of enzyme immunoconjugates and hapten carrier molecule conjugates. It has been used for antibody conjugation and as a protein cross-linker. It is also a glutathione cleavable ADC linker used for the antibody-drug conjugates (ADCs).
(1) J. Carlsson, et al.; Biochem. J. 173, 723 (1978) | (2) D. Pain & A. Surolia; J. Immunol. Methods 40, 219 (1981) | (3) P. Nilsson, et al.; J. Immunol. Methods 41, 81 (1981) | (4) A.F. Habeeb; Biochim. Biophys. Acta 673, 527 (1981) | (5) Y.H. Jou, et al.; Immunol. Commun. 11, 357 (1982) | (6) Y.H. Jou, et al.; Methods Enzymol. 92, 257 (1983)