Skip to Content
Merck
CN

249394

8-Hydroxyjulolidine

96%

Synonym(s):

2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizin-8-ol

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C12H15NO
CAS Number:
Molecular Weight:
189.25
EC Number:
255-247-9
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
Beilstein/REAXYS Number:
1530423
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

8-Hydroxyjulolidine, 96%

InChI key

FOFUWJNBAQJABO-UHFFFAOYSA-N

InChI

1S/C12H15NO/c14-11-6-5-9-3-1-7-13-8-2-4-10(11)12(9)13/h5-6,14H,1-4,7-8H2

SMILES string

Oc1ccc2CCCN3CCCc1c23

assay

96%

form

powder or crystals

composition

Carbon 72.7-79.6%, Nitrogen 7.1-7.7%

color

light brown

mp

132-134 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

Looking for similar products? Visit Product Comparison Guide

General description

The carboxaldehyde derivative of 8-hydroxyjulolidine is useful as a chromophore in fluorescence chemosensor and chemosensors.

Application

8-Hydroxyjulolidine has been used in the electrochemical switching fluorescence study.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

A new multifunctional Schiff base as a fluorescence sensor for Al 3+ and a colorimetric sensor for CN- in aqueous media: an application to bioimaging
Lee SA, et al.
Dalton Transactions, 43(18), 6650-6659 (2014)
Electrochemical switching fluorescence emission in rhodamine derivatives
Cizkova M, et al.
Electrochimica Acta, 260, 589-597 (2018)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service