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About This Item
Empirical Formula (Hill Notation):
C44H30N4
CAS Number:
Molecular Weight:
614.74
UNSPSC Code:
12171500
NACRES:
NA.32
PubChem Substance ID:
EC Number:
213-025-9
Beilstein/REAXYS Number:
379542
MDL number:
product line
BioReagent
Quality Level
assay
≥99.0% (HPLC)
form
crystals
impurities
≤0.5% chlorin
solubility
dichloromethane: soluble
fluorescence
λex 420 nm; λem 651 nm in toluene
suitability
suitable for fluorescence
storage temp.
−20°C
SMILES string
c1ccc(cc1)-c2c3ccc(n3)c(-c4ccccc4)c5ccc([nH]5)c(-c6ccccc6)c7ccc(n7)c(-c8ccccc8)c9ccc2[nH]9
InChI
1S/C44H30N4/c1-5-13-29(14-6-1)41-33-21-23-35(45-33)42(30-15-7-2-8-16-30)37-25-27-39(47-37)44(32-19-11-4-12-20-32)40-28-26-38(48-40)43(31-17-9-3-10-18-31)36-24-22-34(41)46-36/h1-28,45,48H/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-
InChI key
YNHJECZULSZAQK-LWQDQPMZSA-N
Gene Information
human ... TERT(7015)
General description
Tetraphenylporphyrin is a precipitation inhibitor.
Biochem/physiol Actions
Tetraphenylporphyrin serves as an efficient inhibitor for Mg and its alloys. It is mainly used as a porphyrin moiety, in the preparation of ligand and introduction of metal in porphyrin.
Analysis Note
In addition to the emission maximum at 651 nm, there is a lower maxima at 717 nm.
Other Notes
Sensitizer used for the photochemical generation of singlet oxygen
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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