Chemodex

6-Methoxy-N-(3-sulfopropyl)quinolinium

Product Code:
 
CDX-M0051
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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CDX-M0051-M250250 mg£194.00
Quantity:
CDX-M0051-G0011 g£560.00
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Further Information

Alternate Names/Synonyms:
6-Methoxy-N-(3-sulfopropyl)quinolinium; 3-(6Methoxyquinolin-1-ium-1-yl)propane-1-sulfonate; 6-M-Spq
Appearance:
Off-white solid.
CAS:
83907-40-8
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H315, H319, H335
InChi:
InChI=1S/C13H15NO4S/c1-18-12-5-6-13-11(10-12)4-2-7-14(13)8-3-9-19(15,16)17/h2,4-7,10H,3,8-9H2,1H3
InChiKey:
ZVDGOJFPFMINBM-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 83907-40-8. Formula: C13H15NO4S. MW: 281.33. Synthetic. Fluorescent dye to examine and measure membrane chloride transport mechanisms. The fluorescence of SPQ is specifically quenched by chloride via collision. Therefore, the chloride concentration is measured by monitoring the degree of fluorescence decrease. Spectral data: Spectral data: &lambda|ex=~344, &lambda|em=~443.
MDL:
MFCD00037592
Molecular Formula:
C13H15NO4S
Molecular Weight:
281.33
Package Type:
Vial
Precautions:
P261, P280, P305, P351, P338
Product Description:
Fluorescent dye to examine and measure membrane chloride transport mechanisms. The fluorescence of SPQ is specifically quenched by chloride via collision. Therefore, the chloride concentration is measured by monitoring the degree of fluorescence decrease. Spectral data: Spectral data: lambda|ex=~344, lambda|em=~443.
Purity:
>99.0% (N)
Signal word:
Warning
SMILES:
O=S(CCC[N+]1=CC=CC2=CC(OC)=CC=C21)([O-])=O
Solubility Chemicals:
Soluble in water, methanol, DMSO or DMF.
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) O.S. Wolfbeis & E. Urbano; J. Heterocycl. Chem. 19, 841 (1982) | (2) O.S. Wolfbeis & E. Urbano; Fresenius Z. Anal. Chem. 314, 577 (1983) | (3) N.P. Illsley A.S. Verkman; Biochemistry 26, 1215 (1987) | (4) R. Krapf, et al.; Anal. Biochem. 169, 142 (1988) | (5) G. Cabrini; Appl. Fluoresc. Technol. 1, 11 (1989) | (6) A.S. Verkman, et al.; Biochemistry 28, 4240 (1989) | (7) M. Vasseur, et al.; Am. J. Physiol. 264, C27 (1993) | (8) B. Pilas & G. Durack; Cytometry 28, 316 (1997) | (9) R. Shingles, et al.; J. Bioenerg. Biomembr. 29, 611 (1997)