Skip to Content
MilliporeSigma
All Photos(1)

Documents

11627

Sigma-Aldrich

Diethyl azodicarboxylate solution

purum, ~40% in toluene (H-NMR)

Synonym(s):

1,2-Ethoxycarbonyl diazene solution, DEAD, Diethoxycarbonyldiazene solution, Diethyl azodiformate solution, NSC 3474, NSC 679015, Unifoam AZ-AE 200

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C2H5OCON=NCOOC2H5
CAS Number:
Molecular Weight:
174.15
Beilstein/REAXYS Number:
908662
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22

grade

purum

form

solid

concentration

~40% in toluene (H-NMR)

refractive index

n20/D 1.47

storage temp.

2-8°C

SMILES string

CCOC(=O)\N=N/C(=O)OCC

InChI

1S/C6H10N2O4/c1-3-11-5(9)7-8-6(10)12-4-2/h3-4H2,1-2H3/b8-7+

InChI key

FAMRKDQNMBBFBR-BQYQJAHWSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Diethyl azodicarboxylate (DEAD) is a reagent used in the Mitsunobu reaction.
DEAD can also be used as a reagent in the:
  • Synthesis of esters, ethers, amines, and thioethers of alcohols.
  • Oxidation of alcohols to carbonyl derivatives using ZnBr2 as a catalyst via dehydrogenation reaction.
  • Conversion of alcohol to an azide key intermediate in the total synthesis of immunostimulant α-galactosylceramides.
  • Synthesis of aza-β-lactams from aryl(alkyl)ketenes.
  • Synthesis of 1H-1,2,4-triazole-1,4(5H)-dicarboxylate derivatives.
  • Diels-Alder type reactions.

Reactant for preparation of:
  • Immunostimulants α-Galactosylceramides
  • Cellotriose and cellotetraose analogues as transition state mimics for mechanistic studies of cellulases
  • Bisubstrate inhibitors with molecular recognition at the active site of catechol-O-methyltransferase
  • Derivatives of F200 and S383 with cannabinoid CB1 receptor binding activities
  • Aza-β-lactams via NHC-catalyzed [2 + 2] cycloaddition with ketenes

Reagent for:
  • Annulation of N-protected imines
  • α-thiocyanation of enolizable ketones with ammonium thiocyanate
  • Diels-Alder reactions

Other Notes

Reagent used in the Mitsunobu reaction, reviews

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

target_organs

Central nervous system, Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

105.8 °F - closed cup

flash_point_c

41 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and thermolysis of Diels-Alder adducts of 2, 9-dialkylpentacenes with diethyl azodicarboxylate
Okamoto K, et al.
Journal of Physical Organic Chemistry, 21(3), 257-262 (2008)
The Mitsunobu reaction: origin, mechanism, improvements, and applications
But TYS and TPH
Chemistry - An Asian Journal, 2(11), 1340-1355 (2007)
Enantioselective synthesis of aza-β-lactams via NHC-catalyzed [2+ 2] cycloaddition of ketenes with diazenedicarboxylates
Huang X-L, et al.
The Journal of Organic Chemistry, 74(19), 7585-7587 (2009)
Phosphine-mediated annulation of N-protected imines with DEAD
Lian Z, et al.
Tetrahedron, 67(11), 2018-2024 (2011)
Oxime-based linker libraries as a general approach for the rapid generation and screening of multidentate inhibitors
Bahta M, et al.
Nature Protocols, 7(4), 686-686 (2012)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service