Deferoxamine

Also known as: Desferrioxamine B, Deferoxamine B, Desferal, Deferrioxamine, Desferrioxamine, Deferoxaminum, Deferoxamin, Desferin, N-[5-[[4-[5-[acetyl(hydroxy)amino]pentylamino]-4-oxobutanoyl]-hydroxyamino]pentyl]-N'-(5-aminopentyl)-N'-hydroxybutanediamide

Deferoxamine (CAS 70-51-9) is a compound in the Organic Bases category listed in the Jingsj chemical database. It has the molecular formula C25H48N6O8 and a molecular weight of 560.68400 g/mol. Key properties include a melting point of 139°C, a boiling point of 627.9°C (rough estimate) and a density of 1.212g/cm3. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.: 70-51-9
Jingsj CID: J-44564-7
Molecular Formula: C₂₅H₄₈N₆O₈
Molecular Weight: 560.68400 g/mol
Category: Organic Bases
Last updated: 8/21/2026

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Physicochemical Properties

Melting Point	139°C
Boiling Point	627.9°C (rough estimate)
Density	1.212g/cm3
Exact Mass	560.35300
PSA	205.84000
LogP	2.40420
Refractive Index	1.537

Activity & Biological Data

Additional Information	[1]. Duscher D, et al. Comparison of the Hydroxylase Inhibitor Dimethyloxalylglycine and the Iron Chelator Deferoxamine in Diabetic and Aged Wound Healing. Plast Reconstr Surg. 2017 Mar;139(3):695e-706e. [2]. Dongiovanni P, et al. Iron depletion by deferoxamine up-regulates glucose uptake and insulin signaling in hepatoma cells and in rat liver. Am J Pathol. 2008 Mar;172(3):738-47. [3]. Wang G, et al. In vitro assessment of deferoxamine on mesenchymal stromal cells from tumor and bone marrow. Environ Toxicol Pharmacol. 2017 Jan;49:58-64. [4]. Wu Y, et al. Neuroprotection of deferoxamine on rotenone-induced injury via accumulation of HIF-1 alpha and induction of autophagy in SH-SY5Y cells. Neurochem Int. 2010 Oct;57(3):198-205. [5]. Bellotti D, et al. Deferoxamine B: A Natural, Excellent and Versatile Metal Chelator. Molecules. 2021 May 28;26(11):3255.

Additional Information

[1]. Duscher D, et al. Comparison of the Hydroxylase Inhibitor Dimethyloxalylglycine and the Iron Chelator Deferoxamine in Diabetic and Aged Wound Healing. Plast Reconstr Surg. 2017 Mar;139(3):695e-706e. [2]. Dongiovanni P, et al. Iron depletion by deferoxamine up-regulates glucose uptake and insulin signaling in hepatoma cells and in rat liver. Am J Pathol. 2008 Mar;172(3):738-47. [3]. Wang G, et al. In vitro assessment of deferoxamine on mesenchymal stromal cells from tumor and bone marrow. Environ Toxicol Pharmacol. 2017 Jan;49:58-64. [4]. Wu Y, et al. Neuroprotection of deferoxamine on rotenone-induced injury via accumulation of HIF-1 alpha and induction of autophagy in SH-SY5Y cells. Neurochem Int. 2010 Oct;57(3):198-205. [5]. Bellotti D, et al. Deferoxamine B: A Natural, Excellent and Versatile Metal Chelator. Molecules. 2021 May 28;26(11):3255.

Customs & Trade Information

HS Code	2924199090
Summary	2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Frequently Asked Questions

What is the CAS number of Deferoxamine?

The CAS number of Deferoxamine is 70-51-9.

What are the molecular formula and molecular weight of Deferoxamine?

Deferoxamine has molecular formula C25H48N6O8 and molecular weight 560.68400 g/mol.

Data compiled from public chemical databases such as PubChem and supplier catalogs; supplier offers are provided by suppliers.

Last updated: 8/21/2026

How to cite: Jingsj. "Deferoxamine (CAS 70-51-9)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-44564-7 (accessed 2026-11-09).

Data for reference only; verify product details with suppliers before purchase.