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22112-79-4

  • Product Name:5,10,15,20-tetra(3-hydroxyphenyl)porphyrin
  • Molecular Formula:C44H30 N4 O4
  • Molecular Weight:678.747
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Product Details

pd_meltingpoint:>320 °C

Purity:99%

Factory Sells Best Quality 5,10,15,20-tetra(3-hydroxyphenyl)porphyrin 22112-79-4 with steady supply

  • Molecular Formula:C44H30 N4 O4
  • Molecular Weight:678.747
  • Melting Point:>320 °C 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:137.22000 
  • Density:1.401g/cm3 
  • LogP:5.68860 

22112-79-4 Relevant articles

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, (2021)

The development of new antimicrobial str...

The synthesis of new potential photosensitizers

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, p. 627 - 635 (2013)

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, p. 440 - 448 (2013)

Porphyrin compounds having groups that m...

Synthesis, photophysical properties and DNA-Binding Studies of p-Hydroxy and m-Hydroxy Amphiphilic Porphyrins

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Ideal reaction conditions were found to ...

Porphyrin n-pincer pd(Ii)-complexes in water: A base-free and nature-inspired protocol for the oxidative self-coupling of potassium aryltrifluoroborates in open-air

Hanafiah, Marlia M.,Lakkaboyana, Sivarama Krishna,Lakshmidevi, Jangam,Marella, Ravi Kumar,Naidu, Bandameeda Ramesh,Prasad, Sana Siva,Venkateswarlu, Katta

, (2021/09/13)

Metalloporphyrins (and porphyrins) are w...

New approach for the synthesis, docking of new porphyrins and their antitumor activity

Tawfik, Eman H.,Fadda, Ahmed A.,Soliman, Nanees N.,Abou-Zeid, Laila,Negm, Amr

, p. 251 - 259 (2019/02/24)

A new methodology for the synthesis of a...

A four-phenyl porphine production method (by machine translation)

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Paragraph 0059-0062; 0103-0110, (2020/02/07)

The invention discloses a production met...

22112-79-4 Process route

5,10,15,20-tetrakis(3-acetoxyphenyl)-porphyrin

5,10,15,20-tetrakis(3-acetoxyphenyl)-porphyrin

meso-5,10,15,20-tetra(3-hydroxyphenyl)porphine
22112-79-4

meso-5,10,15,20-tetra(3-hydroxyphenyl)porphine

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; water; for 1h; Reflux;
97%
5,10,15,20-tetrakis(3-acetoxyphenyl)-porphyrin; With hydrogenchloride; In ethanol; water; at 90 - 100 ℃; for 1.5h;
With sodium hydroxide; at 20 ℃; for 1h;
In ethyl acetate; at 20 ℃;
89%
pyrrole
109-97-7,30604-81-0

pyrrole

meta-hydroxybenzaldehyde
100-83-4

meta-hydroxybenzaldehyde

meso-5,10,15,20-tetra(3-hydroxyphenyl)porphine
22112-79-4

meso-5,10,15,20-tetra(3-hydroxyphenyl)porphine

Conditions
Conditions Yield
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide;
70%
pyrrole; meta-hydroxybenzaldehyde; With propionic acid; In cyclohexane; at 146.2 ℃; for 0.4h; under 3040.2 Torr;
In cyclohexane; for 0.9h; Reflux;
49.2%
pyrrole; meta-hydroxybenzaldehyde; In cyclohexane; propionic acid; at 146.2 ℃; for 0.4h; under 3040.2 Torr; Large scale; Green chemistry;
With air; In cyclohexane; propionic acid; for 0.9h; Large scale; Green chemistry;
46.3%
With propionic acid; nitrobenzene; at 200 ℃; for 0.0833333h; Microwave irradiation; Sealed vessel;
36%
In water; at 199.84 ℃; for 0.166667h; under 12001.2 Torr; Microwave irradiation; Green chemistry;
11%
With acetic acid; In nitrobenzene; at 120 ℃; for 1h; Inert atmosphere;
10%
With acetic acid; nitrobenzene; at 120 ℃; for 1h;
10%
In propionic acid; for 1.5h; Reflux;
9%
With propionic acid; at 130 ℃; for 1h;
4.4%
With hydrogenchloride; sodium dodecyl-sulfate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; Product distribution; multistep reaction; porphirin yield versus aldehyde concentration;
With propionic acid; at 20 - 140 ℃; for 14h; Heating / reflux;
With trifluoromethane sulfonyl chloride; In dichloromethane; at 20 ℃; Inert atmosphere;
In propionic acid; for 14h; Heating / reflux;
pyrrole; meta-hydroxybenzaldehyde; With propionic acid; propionic acid anhydride; In ethanol; at 140 ℃; for 1h;
In ethanol; at 20 ℃; for 1h;

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