Chemodex

DACM

Product Code:
 
CDX-D0047
Product Group:
 
Dyes, Stains, and Probes
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
-20 °C
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Chemical Structure
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Chemical Structure

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CodeSizePrice
CDX-D0047-M0055 mg£248.00
Quantity:
CDX-D0047-M02525 mg£995.00
Quantity:
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
N-(7-Dimethylamino-4-methylcoumarin-3-yl) maleimide
Appearance:
Orange solid.
CAS:
55145-14-7
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Protect from light and moisture.
Hazards:
H315, H335
InChi:
InChI=1S/C16H14N2O4/c1-9-11-5-4-10(17(2)3)8-12(11)22-16(21)15(9)18-13(19)6-7-14(18)20/h4-8H,1-3H3
InChiKey:
ADEORFBTPGKHRP-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 55145-14-7. Formula: C16H14N2O4. MW: 298.29. Synthetic. Excellent blue fluorescent thiol-reactive reagent (Ex/Em: 383/463nm), widely used for probing configurations of biomolecules such as proteins and create blue-fluorescent bioconjugates. The unreacted reagent is non-fluorescent and can also be used to quantitate free thiols. Shows superior fluorescence and water solubility properties than dansyl chloride.
MDL:
MFCD00006863
Molecular Formula:
C16H14N2O4
Molecular Weight:
298.29
Package Type:
Vial
Precautions:
P261
Product Description:
Excellent blue fluorescent thiol-reactive reagent (Ex/Em: 383/463nm), widely used for probing configurations of biomolecules such as proteins and create blue-fluorescent bioconjugates. The unreacted reagent is non-fluorescent and can also be used to quantitate free thiols. Shows superior fluorescence and water solubility properties than dansyl chloride.
Purity:
>98% (NMR)
Signal word:
Warning
SMILES:
CN(C)C1=CC=C2C(OC(=O)C(N3C(=O)C=CC3=O)=C2C)=C1
Solubility Chemicals:
Soluble in water.
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) L. Pollegioni et al.; Arch. of Biochem. Bioph. 343(1), 1 (1997) | (2) B. Werneburg et al.; Arch. of Biochem. Bioph. 303(2), 214 (1993) | (3) Y. Kanaoka et al.; Angew. Chem. 89, 141 (1977)