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14459-29-1

  • Product Name:HEMATOPORPHYRIN
  • Molecular Formula:C34H38 N4 O6
  • Molecular Weight:598.699
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Product Details

pd_meltingpoint:172.5°C

Purity:99%

Manufacturer supply high quality HEMATOPORPHYRIN 14459-29-1 with GMP standards

  • Molecular Formula:C34H38 N4 O6
  • Molecular Weight:598.699
  • Melting Point:172.5°C 
  • Refractive Index:1.6000 (estimate) 
  • Boiling Point:1192.7°Cat760mmHg 
  • Flash Point:675.1°C 
  • PSA:171.36000 
  • Density:1.32g/cm3 
  • LogP:2.64570 

HEMATOPORPHYRIN(Cas 14459-29-1) Usage

Hazard

Toxic. Reported to be preferentially absorbed by cancerous tissues, making them fluoresce under UV light.

Purification Methods

Purify it by dissolving it in EtOH Hematoporphyrin and adding H2O or Et2O to give deep red crystals. It has also been recrystallised from MeOH. UV has max at 615.5, 565, 534.4 and 499.5nm in 0.1N NaOH, and 597, 619, 634, 653, 683 and 701nm in 2N HCl [Falk Porphyrins and Metalloporphyrins Elsevier, NY, p 175 1964, LCCCNo 63-19821.] It is used in the affinity chromatographic purification of Heme proteins [Olsen Methods Enzymol 123 324 1986]. The O-methyl-dimethyl ester has m 203-206o (from CHCl3/MeOH), and the O,O'-dimethyl-dimethyl ester has m 145o (from CHCl3/MeOH). [Paul Acta Chem Scand 5 389 1951, Beilstein 26 III/IV 3157, and 3158 for the HCl.]

Definition

ChEBI: A dicarboxylic acid that is protoporphyrin in which the vinyl groups at positions 7 and 12 are replaced by 1-hydroxyethyl groups.

InChI:InChI=1/C34H38N4O6/c1-15-21(7-9-31(41)42)27-14-28-22(8-10-32(43)44)16(2)24(36-28)12-29-34(20(6)40)18(4)26(38-29)13-30-33(19(5)39)17(3)25(37-30)11-23(15)35-27/h11-14,19-20,35,38-40H,7-10H2,1-6H3,(H,41,42)(H,43,44)/b23-11-,24-12-,25-11-,26-13-,27-14-,28-14-,29-12-,30-13-

14459-29-1 Relevant articles

Interaction of dicarboxylic metalloporphyrins with liposomes. The effect of pH on membrane binding revisited

Kepczynski, Mariusz,Ehrenberg, Benjamin

, p. 486 - 492 (2002)

The acid-base properties of Zn-hematopor...

Tetrapyrrole hydroxyalkylamide photochemotherapeutic agents

-

, (2008/06/13)

This invention relates to new preparatio...

Antibody-therapeutic agent conjugates

-

, (2008/06/13)

-

The Chemistry of Pyrrolic Compounds. XLV. Haematoporphyrin Derivative: Haematoporphyrin Diacetate as the Main Product of the Reaction of Haematoporphyrin with a Mixture of Acetic and Sulfuric Acids

Clezy, Peter S.,Hai, Ton That,Henderson, Robert W.,Thuc, Le van

, p. 585 - 597 (2007/10/02)

A mixture of acetic and sulfuric acids c...

14459-29-1 Process route

hematoporphyrin
14459-29-1

hematoporphyrin

Conditions
Conditions Yield
Dihydro-haematoporphyrin durch Disproportionierung;
Dihydro-haematoporphyrin,Jod;
Dihydro-haematoporphyrin,Chloranil;
Dihydro-haematoporphyrin,3-;
Dihydro-haematoporphyrin,O2;
Dihydro-haematoporphyrin,andere Oxydationsmittel;
Tetrahydro-haematoporphyrin,Jod;
Tetrahydro-haematoporphyrin,Chloranil;
Tetrahydro-haematoporphyrin,3-;
Tetrahydro-haematoporphyrin,O2;
Tetrahydro-haematoporphyrin,andere Oxydationsmittel;
Hexahydro-haematoporphyrin,Jod;
Hexahydro-haematoporphyrin,Chloranil;
Hexahydro-haematoporphyrin,3-;
Hexahydro-haematoporphyrin,O2;
Hexahydro-haematoporphyrin,andere Oxydationsmittel;
hematoporphyrin
14459-29-1

hematoporphyrin

hematoporphyrin-dimethyl ester
32562-61-1,119366-88-0,119366-89-1,131070-54-7,131070-74-1,6033-09-6

hematoporphyrin-dimethyl ester

Conditions
Conditions Yield

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