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HEMATOPORPHYRIN

Basic information Safety Supplier Related

HEMATOPORPHYRIN Basic information

Product Name:
HEMATOPORPHYRIN
Synonyms:
  • 1,3,5,8-tetramethyl-2,4-bis(alpha-hydroxyethyl)prophine-6,7-dipropionicacid
  • 21h,23h-porphine-2,18-dipropanoicacid,7,12-bis(1-hydroxyethyl)-3,8,13,17-te
  • 7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-18-porphinedipropionicacid
  • hematoporphyrinix
  • ANTI-HPR antibody produced in mouse
  • 7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-21H,23H-Porphine-2,18-dipropanoic acid
  • 7,12-Bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-21H,23H-porphyrin-2,18-dipropionic acid
  • NSC-59265
CAS:
14459-29-1
MF:
C34H38N4O6
MW:
598.69
EINECS:
238-450-7
Mol File:
14459-29-1.mol
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HEMATOPORPHYRIN Chemical Properties

Melting point:
172.5°C
Boiling point:
649.58°C (rough estimate)
Density 
1.328
refractive index 
1.6000 (estimate)
storage temp. 
Sealed in dry,2-8°C
solubility 
DMSO (Sparingly), Methanol (Slightly), Ethyl Acetate (Slightly)
form 
Solid
color 
Purple to Black
Merck 
13,4653
Stability:
Light Sensitive
EPA Substance Registry System
21H,23H-Porphine-2,18-dipropanoic acid, 7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethyl- (14459-29-1)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
RTECS 
TS5500000
8-10-21

MSDS

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HEMATOPORPHYRIN Usage And Synthesis

Uses

antidepressant, antineoplastic

Uses

Hematoporphyrin (Photodyn, Sensibion) is a porphyrin prepared from hemin. It is a derivative of protoporphyrin IX, where the two vinyl groups have been hydrated (coverted to alcohols). It is used as a photosensitizer in photodynamic therapy. Acetylation of hematoporphyrin followed by hydrolysis of the product of that reaction affords a mixture called hematoporphyrin derivative (HPD), which is also used in photodynamic therapy. Hematoporphyrin has also been used as an antidepressant and antipsychotic since the 1920s.

Definition

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

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.]

HEMATOPORPHYRIN Preparation Products And Raw materials

Raw materials

HEMATOPORPHYRINSupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
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021-61259108 18621169097
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Energy Chemical
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021-021-58432009 400-005-6266
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Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696;
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Shanghai Xianhui Pharmaceutical Co., Ltd.
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021-67792654 13564796979
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Shanghai XueEr Pharmaceutical Technology Co., Ltd
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021-34622192 13917187091
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