8-Hydroxyjulolidine-9-aldehyde
| Code | Size | Price |
|---|
| CDX-H0021-G001 | 1 g | £65.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Documents
Further Information
Alternate Names/Synonyms:
9-Formyl-8-hydroxyjulolidine; 9-Formyl-8-julolidinol; 8-Hydroxyjulolidine-9-carboxaldehyde
Appearance:
Grey to green powder.
CAS:
63149-33-7
EClass:
32160000
Form (Short):
solid
GHS Symbol:
GHS07
Handling Advice:
Protect from light and moisture.
Hazards:
H315, H319, H335
InChi:
InChI=1S/C13H15NO2/c15-8-10-7-9-3-1-5-14-6-2-4-11(12(9)14)13(10)16/h7-8,16H,1-6H2
InChiKey:
NRZXBDYODHLZBF-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 63149-33-7. Formula: C13H15NO2. MW: 217.26. Synthetic. Probe that exhibits pH sensitive detection of hydrogen sulfide and silicate in aqueous solution. It displays an excellent selectivity for hydrogen sulfide and silicate over other weak acid salts. The probe detects S2? in live cells, providing a powerful method to study H2S chemistry in biological systems. Used also as an intermediate and building block to synthesize coumarins and other fluorescent compounds and small molecule inhibitors.
MDL:
MFCD00192477
Molecular Formula:
C13H15NO2
Molecular Weight:
217.26
Package Type:
Vial
Precautions:
P261, P305+P351+P338
Product Description:
Probe that exhibits pH sensitive detection of hydrogen sulfide and silicate in aqueous solution. It displays an excellent selectivity for hydrogen sulfide and silicate over other weak acid salts. The probe detects S2? in live cells, providing a powerful method to study H2S chemistry in biological systems. Used also as an intermediate and building block to synthesize coumarins and other fluorescent compounds and small molecule inhibitors.
Purity:
>98% (HPLC)
Signal Word:
Warning
SMILES:
[H]C(C1=CC2=C(C3=C1O)N(CCC3)CCC2)=O
Solubility Chemicals:
Soluble in 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 +4°C.
References
(1) N. Shanker, et al.; J. Fluoresc. 21, 2173 (2011) | (2) Y. Yang, et al.; Sens. Act. B: Chem. 186, 212 (2013) | (3) S. Ranatunga, et al.; J. Med. Chem. 57, 4289 (2014)