Chemodex

3'-O-Methylfluorescein

Product Code:
 
CDX-M0098
Product Group:
 
Dyes, Stains, and Probes
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
-20°C
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Chemical Structure

Chemical Structure

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CDX-M0098-M0055 mg£114.00
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CDX-M0098-M05050 mg£694.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
Methylfluorescein
Appearance:
Light red to brown powder.
CAS:
70672-05-8
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H319
InChi:
InChI=1S/C21H14O5/c1-24-13-7-9-17-19(11-13)25-18-10-12(22)6-8-16(18)21(17)15-5-3-2-4-14(15)20(23)26-21/h2-11,22H,1H3
InChiKey:
KDXNYSZNOWTPLE-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 70672-05-8. Formula: C21H14O5. MW: 346.33. Synthetic Used in fluorimetric studies. Fluorescent probe. Selective fluorometric substrate for CYP2C19 and CYP1A1. Reaction product of the substrate 3-O-methylfluorescein phosphate (OMFP) is hydrolyzed by phosphatases to yield O-methylfluorescein (OMF) that is detected at a 485nm excitation/525nm emission.
MDL:
MFCD00055945
Molecular Formula:
C21H14O5
Molecular Weight:
346.33
Package Type:
Vial
Precautions:
P305, P351, P338
Product Description:
Used in fluorimetric studies. Fluorescent probe. Selective fluorometric substrate for CYP2C19 and CYP1A1. Reaction product of the substrate 3-O-methylfluorescein phosphate (OMFP) is hydrolyzed by phosphatases to yield O-methylfluorescein (OMF) that is detected at a 485nm excitation/525nm emission.
Purity:
>97% (HPLC)
Signal word:
Warning
SMILES:
COC1=CC2=C(C=C1)C1(OC(=O)C3=C1C=CC=C3)C1=CC=C(O)C=C1O2
Solubility Chemicals:
Soluble in DMSO.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) M. Brisson Tierno, et al.; Nat. Protocols 2, 1134 (2007) | (2) S. Sudsakorn, et al.; DMD 35, 841 (2007) | (3) E. Sergienko, et al.; ACS Chem. Biol. 7, 367 (2012)