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16009-13-5

  • Product Name:Hemin
  • Molecular Formula:C34H32ClFeN4O4
  • Molecular Weight:651.952
  • Appearance:Dark purple crystalline powder
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Product Details

pd_meltingpoint:300 °C

Appearance:Dark purple crystalline powder

Purity:99%

Excellent chemical plant bulk supply Hemin 16009-13-5

  • Molecular Formula:C34H32ClFeN4O4
  • Molecular Weight:651.952
  • Appearance/Colour:Dark purple crystalline powder 
  • Melting Point:300 °C 
  • PSA:109.18000 
  • LogP:4.29920 

Hemin(Cas 16009-13-5) Usage

General Description

Heme is a small molecule present either free or bound to hemoglobin in the bloodstream of mammals. This is an alternative source of iron within the host that contains a porphyrin ring containing a Fe2+ ion called hemin.

Biochem/physiol Actions

Hemin, the oxidized version of heme, is an iron-containing prosthetic group for a diverse group of proteins. Free heme, which can be released from hemoglobin following hemolysis, is pro-inflammatory and contributes to iron-derived reactive oxygen species. Free hemin levels may be upregulated in various pathological conditions and can contribute to various inflammatory conditions including vascular disorders, renal failure, and immune-mediated disorders.Hemin may be used to study the expression and represson of heme oxygenase 1 (HO-1) as well as the activity of HO-1. Hematin is the "X factor" required to grown Haemophilus influenzae.

Purification Methods

Hemin is purified by recrystallisation from AcOH. Also, hemin (5g) is shaken in pyridine (25mL) till it dissolves, then CHCl3 (40mL) is added, the container is stoppered and shaken for 5minutes (releasing the stopper occasionally). The solution is filtered under slight suction, and the flask and filter are washed with a little CHCl3 (15mL). During this period, AcOH (300mL) is heated to boiling, and saturated aqueous NaCl (5mL) and conc HCl (4mL) are added. The CHCl3 filtrate is poured in a steady stream, with stirring, into the hot AcOH mixture and set aside for 12hours. The crystals are filtered off, washed with 50% aqueous AcOH (50mL), H2O (100mL), EtOH (25mL), Et2O and dried in air. [Fischer Org Synth Coll Vol III 442 1955, Beilstein 26 III/IV 3048.]

InChI:InChI=1/C34H34N4O4.ClH.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);1H;/q;;+3/p-3/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;;/rC34H32ClFeN4O4/c1-7-21-17(3)26-14-31-22(8-2)19(5)29-13-25-18(4)23(9-11-33(41)42)28(38-25)16-32-24(10-12-34(43)44)20(6)30(15-27(21)37-26)40(32)36(35)39(29)31/h7-8,13-16H,1-2,9-12H2,3-6H3,(H,41,42)(H,43,44)/b25-13-,26-14-,27-15-,28-16-,29-13-,30-15-,31-14-,32-16-

16009-13-5 Relevant articles

Impact of metal ions in porphyrin-based applied materials for visible-light photocatalysis: Key information from ultrafast electronic spectroscopy

Kar, Prasenjit,Sardar, Samim,Alarousu, Erkki,Sun, Jingya,Seddigi, Zaki S.,Ahmed, Saleh A.,Danish, Ekram Y.,Mohammed, Omar F.,Pal, Samir Kumar

, p. 10475 - 10483 (2014/08/18)

ProtoporphyrinIX-zinc oxide (PP-ZnO) nan...

Haem-Biosynthese aus L-Glutaminsaeure

Franck, Burchard,Bruse, Manfred,Dahmer, Juergen

, p. 1000 - 1001 (2007/10/02)

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16009-13-5 Process route

iron(III) chloride

iron(III) chloride

protoporphyrin IX
553-12-8

protoporphyrin IX

iron(III) protoporphyrin IX chloride
13496-05-4,16009-13-5

iron(III) protoporphyrin IX chloride

Conditions
Conditions Yield
In water; dimethyl sulfoxide; for 12h;
L-glutamic acid
56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6

L-glutamic acid

(SP-5-13)-chloro(7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato<sup>(4-)</sup>-N<sub>21</sub>,N<sub>22</sub>,N<sub>23</sub>,N<sub>24</sub>)-ferrate<sup>(2-)</sup>, dihydrogen
16009-13-5

(SP-5-13)-chloro(7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-N21,N22,N23,N24)-ferrate(2-), dihydrogen

Conditions
Conditions Yield
for 24h; radioactivity investigations with duck blood;

16009-13-5 Upstream products

  • 56-86-0
    56-86-0

    L-glutamic acid

  • 553-12-8
    553-12-8

    protoporphyrin IX

16009-13-5 Downstream products

  • 927179-10-0
    927179-10-0

    heme b

  • 15489-90-4
    15489-90-4

    ferriprotoporphyrin IX hydroxide

  • 5522-66-7
    5522-66-7

    protoporphyrin IX dimethyl ester

  • 26280-00-2
    26280-00-2

    biliverdin IXγ dimethyl ester

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