HEMATIN

HEMATIN Suppliers list
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Tel: 89508211 18501085097
Email: sales.bj@hwrkchemical.com
Company Name: Sichuan Kulinan Technology Co., Ltd  
Tel: 400-1166-196 18981987031
Email: cdhxsj@163.com
Company Name: Hunan Hui Bai Shi Biotechnology Co., Ltd.  
Tel: 0731-85526065 13308475853
Email: ivy@hnhbsj.com

HEMATIN manufacturers

  • HEMATIN
  • HEMATIN pictures
  • $1.10
  • 2026-08-20
  • CAS:15489-90-4
  • Min. Order: 1g
  • Purity: 99.9% Min
  • Supply Ability: 100 Tons
  • HEMATIN
  • HEMATIN pictures
  • 2026-06-30
  • CAS:15489-90-4
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1000 kg
  • Hematin
  • Hematin pictures
  • $42.00
  • 2026-05-11
  • CAS:15489-90-4
  • Purity: 99.25%
  • Supply Ability: 10g
HEMATIN Basic information
Description References
Product Name:HEMATIN
Synonyms:2-))-hydroxy-;ferrihemate;ferriheme;ferrihemehydroxide;ferrihemicacid;HEMATEIN;HEMATIN PORCINE;HYDROXYHEMIN
CAS:15489-90-4
MF:C34H31FeN4O5-
MW:631.49
EINECS:239-518-9
Product Categories:HematinApplication Index;Plasma&Blood Proteins;Plasma, Blood, and Related Proteins and Reagents;Serum Proteins;Serum Proteins and Related Enzymes
Mol File:15489-90-4.mol
HEMATIN Structure
HEMATIN Chemical Properties
Melting point 180 °C
storage temp. 2-8°C
solubility DMF (Slightly), DMSO (Slightly, Heated, Sonicated), Pyridine (Slightly, Heated,
form solid
color Black
biological sourcePorcine
Merck 14,4635
Stability:Light Sensitive
Cosmetics Ingredients FunctionsHAIR CONDITIONING
InChIKeyBMUDPLZKKRQECS-HXFTUNQESA-K
SMILESCc1c(CCC(O)=O)c2cc3c(CCC(O)=O)c(C)c4cc5nc(cc6c(C=C)c(C)c(cc1n2)n6[Fe](O)n34)c(C)c5C=C
LogP7.193 (est)
CAS DataBase Reference15489-90-4
Safety Information
WGK Germany 3
RTECS NO6725000
HS Code 2934999090
Storage Class11 - Combustible Solids
ToxicityLD50 i.v. in rats: 4.32 mg/100 g (Lips)
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
HEMATIN Usage And Synthesis
DescriptionProduced from red blood cells, Hematin is a bluish-black or brownish pigment compound derived from hemoglobin by removal of the protein part and oxidation of the iron atom from ferrous Fe2+ to the ferric Fe3+ state, which does not combine with oxygen. It is effective to inhibit the synthesis of porphyrin and, at the same time, stimulate the synthesis of globin. It involves in the formation of cytochromes and peroxidases in the cell. Hematin is also a pharmaceutical used in the treatment of porphyria, which can be administered intravenously to halt the attack of acute porphyria. It functions in the liver to accelerate the production of heme and thus preventing the further accumulation of heme precursors, porphyrins, which is effective to alleviate the symptoms of porphyria.
Referenceshttps://en.wikipedia.org/wiki/Haematin
http://house.wikia.com/wiki/Hematin
https://en.oxforddictionaries.com/definition/us/hematin
http://medical-dictionary.thefreedictionary.com/hematin
Chemical PropertiesDark crystals with metalic luster
UsesIndicator, biological stain.
UsesHematin was used in a study to test in vitro activities of the Rx-01 oxazolidinones against hospital and community pathogens. It was also used in a study to test in-vitro bacterial identification using fluorescence spectroscopy with an optical fiber system.
DefinitionThe hydroxide of heme. Not to be confused with hematein.
Biological ActivityHematin is a hydroxide of heme. It may be used to tre at acute porphyric attacks. Hematin suppresses the hepatic aminolevulinic acid (ALA) function and replenishes cytochrome action by restoring the endogenous heme deficit. Early administration of hematin can prevent irreversible neuronal damage induced due to metabolic disorders.
SynthesisHeme synthesis involves a seven-step enzymatic pathway, commencing with the condensation of glycine and succinyl-CoA to form δ-aminolevulinic acid (ALA). Subsequently, ALA is converted into porphyrinogen (PBG), which is further transformed into porphyrin IX. Ultimately, porphyrin IX binds with iron to form haem. The initial steps of this process occur within the mitochondria, whilst subsequent reactions take place in the cytoplasm. The specific steps are as follows:
(1) Condensation of Glycine and Succinyl-CoA (Enzyme: ALA synthase)
Reaction: Glycine + Succinyl-CoA → δ-aminolevulinic acid (ALA)
(2) Formation of Porphobilinogen (PBG) (Enzyme: ALA dehydratase)
Reaction: 2 ALA → PBG + 2 H2O
(3) Conversion of Porphobilinogen to Uroporphyrinogen III (Enzyme: Porphobilinogen deaminase)
Reaction: 4 PBG → Hydroxymethylbilane + 3 H2O
(4) Decarboxylation of Uroporphyrinogen III (Enzyme: Uroporphyrinogen decarboxylase)
Reaction: Hydroxymethylbilane → Uroporphyrinogen III + CO2 + H2O
(5) Oxidative Decarboxylation of Coproporphyrinogen III (Enzyme: Coproporphyrinogen oxidase)
Reaction: Coproporphyrinogen III → Protoporphyrinogen IX + CO2 + 2H2O
(6) Conversion of Protoporphyrinogen IX to Protoporphyrin IX  (Enzyme: Protoporphyrinogen oxidase)
Reaction: Protoporphyrinogen IX → Protoporphyrin IX + H2O
(7) Insertion of Iron into Protoporphyrin IX (Enzyme: Ferrochelatase)
Reaction: Protoporphyrin IX + Fe2+ → Heme
Heme Synthesis
Purification MethodsCrystallise it from pyridine. Dry it at 40o in vacuo.[Beilstein 26 III/IV 3047.]
HEMATIN Preparation Products And Raw materials
Tag:HEMATIN(15489-90-4) Related Product Information
Hemin Cytochrome C HEMATEIN,HEMATEIN FOR MICROSCOPY,HEMATEIN FROM LOGWOOD,HEMATEIN C.I. 75290 FOR MICROSCOPY,HEMATEIN, STAIN 2,4-Dimethylpyrrole 2,3,4,5-TETRAMETHYLPYRROLE Allylacetic acid 6-Heptenoic acid 3-BUTEN-1-AMINE HEMATIN 4-HEXENOIC ACID 1,3,6-HEPTATRIENE N-PROPYLETHYLIDENEAMINE 3-METHYL-2-BUTEN-1-AMINE 5-METHYL-4-HEXENOIC ACID AMMONIUM HEMATEIN,HEMATEIN-AMMONIUM 3-ETHYL-2-METHYL-2-PENTENE HEPTA-4,6-DIENOIC ACID 2,4-OCTADIENE