Chemodex

N-Succinimidyl 3-(2-pyridyldithio)propionate

CHF 97.00
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CDX-S0019-M02525 mgCHF 97.00
CDX-S0019-M100100 mgCHF 296.00
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Product Details
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

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Our product description may differ slightly from the original manufacturers 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.
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Product Specification Sheet
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Description

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).

Product References

(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)

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