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Chemodex
Phenylmethylsulfonyl fluoride
As low as
26
CHF
CHF 26.00
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CDX-P0492-G0011 gCHF 26.00
CDX-P0492-G0055 gCHF 39.00
CDX-P0492-G02525 gCHF 116.00
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Product Details | |
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Synonyms | α-Toluenesulfonyl fluoride; Benzylsulfonyl fluoride; PMSF; Phenylmethanesulfonyl fluoride; NSC 88499 |
Product Type | Chemical |
Properties | |
Formula | C7H7FO2S |
MW | 174.19 |
CAS | 329-98-6 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥99% (GC) |
Appearance | White to faint yellow powder or crystals. |
Solubility | Soluble in DMF (20 mg/ml), DMSO (20 mg/ml) or ethanol (20 mg/ml). |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | YBYRMVIVWMBXKQ-UHFFFAOYSA-N |
Smiles | O=S(CC1=CC=CC=C1)(F)=O |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +20°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 RT. |
Documents | |
Product Specification Sheet | |
Datasheet |
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Description
Phenylmethylsulfonyl fluoride (PMSF) is a potent nonspecific, irreversible inhibitor of serine proteases and other enzymes, including acetylcholinesterase, palmityl coenzyme A deacylase, arylsulfatase A, chymotrypsin, and trypsin widely used in biochemical and molecular biology workflows to protect proteins from proteolytic degradation. It is used in protein solublization studies in order to deactivate proteases from digesting proteins of interest after cell lysis. Because PMSF specifically sulfonylates the hydroxal groups of active site serine residues of enzymes, it can be used as a chemical label to identify essential active site serines in an enzyme. PMSF is known to alter the actions of anandamide by blocking its metabolism and can produce cannabinoid effects in mice, including antinociception, hypothermia, and immobility with ED50 values of 86, 224, and 206 mg/kg, respectively. It is also used as a potentiator of neuropathy.
Product References
(1) P. Turini, et al.; J. Pharmacol. Exp. Ther. 167, 98 (1969) | (2) V. Sekar & J.H. Hageman; BBRC 89, 474 (1979) | (3) D.R. Compton & B.R. Martin; J. Pharmacol. Exp. Ther. 283, 1138 (1997) | (4) K.A. Skau & M.T. Shipley; Neuropharmacol. 38, 691 (1999) | (5) D. Kraut, et al.; Mol. Pharmacol. 57, 1243 (2000) | (6) Q.S. Wang, et al.; Acta Pharmacol. Sin. 22, 249 (2001) | (7) F. Song, et al.; Toxicology 262, 258 (2009) | (8) I. Mangas, et al.; Chem. Res. Toxicol. 25, 2393 (2012)