Skip to Content
Merck
All Photos(1)

Documents

381896

Sigma-Aldrich

2,3-Naphthalocyanine

Dye content 95 %

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C48H26N8
CAS Number:
23627-89-6
Molecular Weight:
714.77
Beilstein:
4345876
MDL number:
MFCD00134560
UNSPSC Code:
12352103
PubChem Substance ID:
57649813
NACRES:
NA.23

composition

Dye content, 95%

Quality Level

100

λmax

712 nm

SMILES string

c1ccc2cc3c4nc(nc5[nH]c(nc6nc(nc7[nH]c(n4)c8cc9ccccc9cc78)c%10cc%11ccccc%11cc6%10)c%12cc%13ccccc%13cc5%12)c3cc2c1

InChI

1S/C48H26N8/c1-2-10-26-18-34-33(17-25(26)9-1)41-49-42(34)54-44-37-21-29-13-5-6-14-30(29)22-38(37)46(51-44)56-48-40-24-32-16-8-7-15-31(32)23-39(40)47(52-48)55-45-36-20-28-12-4-3-11-27(28)19-35(36)43(50-45)53-41/h1-24H,(H2,49,50,51,52,53,54,55,56)

InChI key

LKKPNUDVOYAOBB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

M Soncin et al.
Journal of photochemistry and photobiology. B, Biology, 42(3), 202-210 (1998-05-22)
The photosensitizing activity of the new far-red absorbing naphthalocyanine SiNc [OSi (n-C10H21)3] [OSi(CH3)2(CH2)3N(CH3)2], (DAP-SiNc), and of its analogue SiNc [OSi(i-C4H9)2(n-C18H37)]2, (IsoBO-SiNc), was studied with two cell variants of B16 melanoma, the amelanotic clone B78H1 and the highly pigmented B16F1 cells.
Atsuko Hirao et al.
Chemical communications (Cambridge, England), (39)(39), 4714-4716 (2008-10-03)
Soluble precursors of 2,3-naphthalocyanine (Nc) and phthalocyanine (Pc) were prepared and were converted into insoluble semiconducting thin films of Pc and Nc by heating after fabrication via spin-coating.
Leo Gross
Nature chemistry, 3(4), 273-278 (2011-03-25)
Recently scanning probe microscopy has made tremendous progress in imaging organic molecules with high lateral resolution. Atoms and bonds within individual molecules have been clearly resolved, indicating the exciting potential of this technique for studying molecular structures, bonding within and
C Bellemo et al.
Cancer letters, 65(2), 145-150 (1992-08-14)
A water-soluble derivative of the highly hydrophobic molecule Si(IV)-naphthalocyanine was synthesized by the addition of two polyethyleneglycol ligands in axial positions to the centrally coordinated Si(IV) ion. The compound can be intravenously injected in homogeneous aqueous solution, where it is
Juxiang Zhang et al.
Macromolecular bioscience, 20(8), e2000128-e2000128 (2020-06-23)
Conjugated polymer dots have excellent fluorescence properties in terms of their structural diversity and functional design, showing broad application prospects in the fields of biological imaging and biosensing. Polymer dots contain no heavy metals and are thought to be of
View All Related Papers

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