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381896

Sigma-Aldrich

2,3-Naphthalocyanine

Dye content 95 %

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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%

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

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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’.

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Xiaoning Li et al.
Theranostics, 8(3), 767-784 (2018-01-19)
Fluorescence image-guided surgery combined with intraoperative therapeutic modalities has great potential for intraoperative detection of oncologic targets and eradication of unresectable cancer residues. Therefore, we have developed an activatable theranostic nanoplatform that can be used concurrently for two purposes: (1)
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
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.
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