Basic information Safety Supplier Related

PORPHOBILINOGEN

Basic information Safety Supplier Related

PORPHOBILINOGEN Basic information

Product Name:
PORPHOBILINOGEN
Synonyms:
  • PBG
  • 5-(aminomethyl)-4-(carboxymethyl)-1h-pyrrole-3-propanoicaci
  • PORPHOBILINOGEN
  • porphobilinogen (synth.)
  • 5-(aminomethyl)-4-(carboxymethyl)-1H-pyrrole-3-propionic acid
  • 3-[5-(aminomethyl)-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid
  • 5-[AMINOMETHYL]-4-[CARBOXYMETHYL]-1H-PYRROLE-3-PROPANOIC ACID
  • 5-(Aminomethyl)-4-(carboxymethyl)pyrrole-3-propionic acid
CAS:
487-90-1
MF:
C10H14N2O4
MW:
226.23
EINECS:
207-666-3
Product Categories:
  • organic building block
  • Porphyrins
  • Precursers
  • Amines
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Elisa Kit-plant ELISA Kit
Mol File:
487-90-1.mol
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PORPHOBILINOGEN Chemical Properties

Melting point:
174-177℃
Boiling point:
479℃
Density 
1.421
Flash point:
243℃
storage temp. 
-20°C
solubility 
Aqueous Base (Slightly), Acetonitrile (Slightly), DMSO (Slightly)
pka
4.22±0.10(Predicted)
form 
powder
color 
light yellow to pink
Merck 
13,7681
BRN 
220051
EPA Substance Registry System
Porphobilinogen (487-90-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
8-10

MSDS

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PORPHOBILINOGEN Usage And Synthesis

Uses

An intermediate in the biosynthesis of Heme, found in the urine of patients with acute porphyria.

Definition

ChEBI: Porphobilinogen is a dicarboxylic acid that is pyrole bearing aminomethyl, carboxymethyl and 2-carboxyethyl substituents at positions 2, 3 and 4 respectively. It has a role as a metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a member of pyrroles, a dicarboxylic acid and an aralkylamino compound. It is a conjugate acid of a porphobilinogen(1-).

Biochem/physiol Actions

Intermediate in the biosynthesis of heme.

Purification Methods

Porphobilinogen recrystallises as the monohydrate (pink crystals) from dilute NH4 OAc solutions of pH 4, and is dried in vacuo. The hydrochloride monohydrate has m 165-170o(dec) (from dilute HCl). [Jackson & MacDonald Can J Chem 35 715 1957, Westall Nature 170 614 1952, Bogarad J Am Chem Soc 75 3610 1953, Beilstein 22/14 V 210.]

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