Chemodex

4-Methylumbelliferyl palmitate

CHF 95.00
In stock
CDX-P0038-M250250 mgCHF 95.00
CDX-P0038-G0011 gCHF 285.00
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Product Details
Synonyms 4-MUP; 4-MU Palmitate; 4-Methyl-2-oxo-2H-chromen-7-yl palmitate; Palmitic acid 4-methylumbelliferyl ester
Product Type Chemical
Properties
Formula

C26H38O4

MW 414.59
CAS 17695-48-6
Purity Chemicals ≥95% (NMR)
Appearance White to off-white crystalline powder.
Solubility Soluble in DCM (10mg/ml), chloroform (20mg/ml) or DMF (10mg/m).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key QKQVFFACWLFRRX-UHFFFAOYSA-N
Smiles O=C1OC2=CC(OC(CCCCCCCCCCCCCCC)=O)=CC=C2C(C)=C1
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 -20°C.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

4-Methylumbelliferyl palmitate (4-MUP) is a fluorogenic substrate for lysosomal acid lypase (LAL). 4-MUP is cleaved by LAL (or by other acid lipases) to release the fluorescent moiety 4-MU. Recent advances allow the assessment of LAL activity in very small blood volumes using 4-MUP. Cholesterol ester storage disease and Wolman disease are recessive autosomal disorders caused by a deficiency in lysosomal acid lipase (LAL), also known as cholesteryl ester hydrolase. Spectral data: 4-MU fluorescence is pH-dependent. λex 320nm (pH 1.97-6.72) and 360nm (pH 7.12-10.3); λem 445-455nM (increasing as pH decreases).

Product References

(1) G.J. Guy & J. Butterworth; Clin. Chim. Acta 84, 361 (1978) | (2) S. Kelly & R. Bakhru-Kishore; Clin. Chim. Acta 97, 239 (1979) | (3) T.G. Warner, et al.; Am. J. Hum. Gen. 32, 869 (1980) | (4) T.G. Warner, et al.; J. Biol. Chem. 256, 2952 (1981) | (5) M.W. Baillargeon & S.G. McCarthy; Lipids 26, 831 (1991) | (6) J. Hamilton, et al.; Clin. Chim. Acta 413, 1207 (2012) | (7) H. Zhi, et al.; J. Spectrosc. 1, 147128 (2013) | (8) T. Dairaku, et al.; Mol. Gen. Metab. 111, 193 (2014)

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