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MedKoo Cat#: 161148 | Name: meso-Tetra (4-aminophenyl) Porphine
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

meso-Tetra (4-aminophenyl) Porphine is a synthetic porphyrin product. meso-Tetra (4-aminophenyl) Porphine is used in the creation of both metallic organic frameworks and covalent organic frameworks. meso-Tetra (4-aminophenyl) Porphine is a catalyst for the electrochemical reduction of carbon dioxide.

Chemical Structure

meso-Tetra (4-aminophenyl) Porphine
meso-Tetra (4-aminophenyl) Porphine
CAS#22112-84-1

Theoretical Analysis

MedKoo Cat#: 161148

Name: meso-Tetra (4-aminophenyl) Porphine

CAS#: 22112-84-1

Chemical Formula: C44H34N8

Exact Mass: 674.2906

Molecular Weight: 674.81

Elemental Analysis: C, 78.32; H, 5.08; N, 16.61

Price and Availability

Size Price Availability Quantity
100mg USD 480.00 2 Weeks
250mg USD 700.00 2 Weeks
500mg USD 1,005.00 2 Weeks
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Related CAS #
No Data
Synonym
meso-Tetra(4-aminophenyl) Porphine; meso-Tetra (4-aminophenyl) Porphine; 4,4',4'',4'''-(porphyrin-5,10,15,20-tetrayl)tetraaniline; 4,4',4'',4''' (porphyrin-5,10,15,20-tetrayl)tetraaniline;
IUPAC/Chemical Name
4,4',4'',4'''-(porphyrin-5,10,15,20-tetrayl)tetraaniline
InChi Key
REPFNYFEIOZRLM-LWQDQPMZSA-N
InChi Code
InChI=1S/C44H34N8/c45-29-9-1-25(2-10-29)41-33-17-19-35(49-33)42(26-3-11-30(46)12-4-26)37-21-23-39(51-37)44(28-7-15-32(48)16-8-28)40-24-22-38(52-40)43(36-20-18-34(41)50-36)27-5-13-31(47)14-6-27/h1-24,49,52H,45-48H2/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-
SMILES Code
NC1=CC=C(/C2=C(N/3)\C=CC3=C(C4=CC=C(N)C=C4)\C(C=C/5)=NC5=C(C6=CC=C(/C(C7=CC=C(N)C=C7)=C8N=C2C=C\8)N6)\C9=CC=C(N)C=C9)C=C1
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 674.81 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1.) Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores, Shinde, Digambar Balaji; Kandambeth, Sharath; Pachfule, Pradip; Kumar, Raya Rahul; Banerjee, Rahul, Chemical Communications (Cambridge, United Kingdom) (2015), 51(2), 310-313. 2.) Manganese porphyrin derivatives as ionophores for thiocyanate-selective electrodes: the influence of porphyrin substituents and additives on the response properties Khorasani, Jafar H.; Amini, Mohammad K.; Motaghi, Hasan; Tangestaninejad, Shahram; Moghadam, Majid, Sensors and Actuators, B: Chemical (2002), 87(3), 448-456. 3.) Positional effects of second-sphere amide pendants on electrochemical CO2 reduction catalyzed by iron porphyrins, Nichols, Eva M.; Derrick, Jeffrey S.; Nistanaki, Sepand K.; Smith, Peter T.; Chang, Christopher J., Chemical Science (2018), 9(11), 2952-2960. 4.) The optical gas-sensing properties of an asymmetrically substituted porphyrin, Pedrosa, Jose Ma; Dooling, Colin M.; Richardson, Tim H.; Hyde, Robert K.; Hunter, Chris A.; Martin, Ma Teresa; Camacho, Luis, Journal of Materials Chemistry (2002), 12(9), 2659-2664. 5.) Micellar Cobaltporphyrin Nanorods in Alcohols, Yuasa, Makoto; Oyaizu, Kenichi; Yamaguchi, Aritomo; Kuwakado, Michi, Journal of the American Chemical Society (2004), 126(36), 11128-11129. 6.) Influence of Molecular Organization of Asymmetrically Substituted Porphyrins on Their Response to NO2 Gas, Pedrosa, Jose M.; Dooling, Colin M.; Richardson, Tim H.; Hyde, Robert K.; Hunter, Chris A.; Martin, Maria T.; Camacho, Luis, Langmuir (2002), 18(20), 7594-7601. 7.) State-of-the-art catechol porphyrin COF catalyst for chemical fixation of carbon dioxide via cyclic carbonates and oxazolidinones, Saptal, Vitthal; Shinde, Digambar Balaji; Banerjee, Rahul; Bhanage, Bhalchandra M., Catalysis Science & Technology (2016), 6(15), 6152-6158. 8.) Spin effects on decay dynamics of charge-separated states generated by photoinduced electron transfer in zinc porphyrin-naphthalenediimide dyads, Mori, Yukie; Sakaguchi, Yoshio; Hayashi, Hisaharu , Journal of Physical Chemistry A (2002), 106(18), 4453-4467. 9.) Stable Binding of Isothiocyanoporphyrin Molecules to Au(111): An STM Study, Han, Wenhai; Li, Shumin; Lindsay, S. M.; Gust, Devens; Moore, Thomas A.; Moore, Ana L., Langmuir (1996), 12(23), 5742-5744. 10.) A porous porphyrin organic polymer (PPOP) for visible light triggered hydrogen production, Mukherjee, Gargi; Thote, Jayshri; Aiyappa, Harshitha Barike; Kandambeth, Sharath; Banerjee, Subhrashis; Vanka, Kumar; Banerjee, Rahul, Chemical Communications (Cambridge, United Kingdom) (2017), 53(32), 4461-4464. 11.) Efficient ternary organic photovoltaics incorporating a graphene-based porphyrin molecule as a universal electron cascade materials, Stylianakis, M. M.; Konios, D.; Kakavelakis, G.; Charalambidis, G.; Stratakis, E.; Coutsolelos, A. G.; Kymakis, E.; Anastasiadis, S. H., Nanoscale (2015), 7(42), 17827-17835.