Skip to Content
Merck
All Photos(1)

Key Documents

235563

Sigma-Aldrich

N,N′-Di-tert-butylcarbodiimide

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3CN=C=NC(CH3)3
CAS Number:
Molecular Weight:
154.25
Beilstein:
1758049
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:

Quality Level

Assay

99%

reaction suitability

reaction type: Coupling Reactions

refractive index

n20/D 1.428 (lit.)

bp

48-50 °C/12 mmHg (lit.)

density

0.8 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)N=C=NC(C)(C)C

InChI

1S/C9H18N2/c1-8(2,3)10-7-11-9(4,5)6/h1-6H3

InChI key

IDVWLLCLTVBSCS-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

Application

N,N′-Di-tert-butylcarbodiimide can be used:
  • As a reagent for the guanylation of aryl amines catalyzed by lanthanum amides.
  • To prepare dichloroimidazolidine-4,5-dione by reacting with oxalyl chloride, which is a key intermediate for the synthesis of N,N′-diamidocarbenes.
  • To prepare the iridium complex of benzamidine named Ir(FMeppy)2(N,N′-di-tert-butyl-4-methyl-benzamidine).

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

95.0 °F - closed cup

Flash Point(C)

35 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Customers Also Viewed

Qinghai Li et al.
The Journal of organic chemistry, 72(18), 6763-6767 (2007-08-07)
It is demonstrated that the cyclopentadienyl-free simple lanthanide amides [(Me(3)Si)(2)N](3)Ln(mu-Cl)Li(THF)(3)(Ln = La, Sm, Eu, Y, Yb) and Ln[N(SiMe(3))(2)]3 (Ln = Y, Yb) are highly efficient catalysts for the guanylation of both aromatic and secondary amines with a high activity under
Synthesis, characterization and photophysical properties of iridium complexes with amidinate ligands
Sahin C, et al.
Journal of Organometallic Chemistry, 772, 68-78 (2014)

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