Skip to Content
Merck
CN

247405

N-[5-(Phenylamino)-2,4-pentadienylidene]aniline monohydrochloride

98%

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C6H5NHCH=CHCH=CHCH=NC6H5·HCl
CAS Number:
1497-49-0
Molecular Weight:
284.78
NACRES:
NA.47
PubChem Substance ID:
24854868
UNSPSC Code:
12171500
EC Number:
216-094-3
MDL number:
MFCD00012630

Key Documents

View All Documentation
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

N-[5-(Phenylamino)-2,4-pentadienylidene]aniline monohydrochloride, 98%

InChI key

VUCMMJBDNXZQDJ-SAIFEKGMSA-N

InChI

1S/C17H16N2.ClH/c1-4-10-16(11-5-1)18-14-8-3-9-15-19-17-12-6-2-7-13-17;/h1-15,18H;1H/b9-3+,14-8+,19-15+;

SMILES string

C1(N/C=C/C=C/C=N/C2=CC=CC=C2)=CC=CC=C1.Cl

assay

98%

form

powder or chunks

mp

173-175 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

200

Related Categories

Application

Tricarbocyanine laser dye intermediate

pictograms

Exclamation mark
GHS07

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
SHBP0386
SHBQ9648
SHBP4536
SHBP2376
MKCP3899

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Natalia G Zhegalova et al.
Contrast media & molecular imaging, 9(5), 355-362 (2014-04-26)
Self-aggregation of dyes even at low concentrations poses a considerable challenge in preparing sufficiently bright molecular probes for in vivo imaging, particularly in the conjugation of near infrared cyanine dyes to polypeptides with multiple labeling sites. Such self-aggregation leads to
Duanwen Shen et al.
Scientific reports, 3, 1697-1697 (2013-04-23)
Using a newly developed near-infrared (NIR) dye that fluoresces at two different wavelengths (dichromic fluorescence, DCF), we discovered a new fluorescent substrate for Akt, also known as protein kinase B, and a method to quantitatively report this enzyme's activity in

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