N,N'-Diisopropylcarbodiimide

N,N′-Diisopropylcarbodiimide

Names
Preferred IUPAC name N,N'-Di(propan-2-yl)methanediimine
Other names Diisopropylmethanediimine
Identifiers
CAS Number	693-13-0 Y
3D model (JSmol)	Interactive image
Abbreviations	DIC, DIPC
Beilstein Reference	878281
ChEBI	CHEBI:53092
ChEMBL	ChEMBL1332992
ChemSpider	12211 N
ECHA InfoCard	100.010.677
EC Number	211-743-7
Gmelin Reference	101400
PubChem CID	12734
UNII	OQO20I6TWH
CompTox Dashboard (EPA)	DTXSID4025086
InChI InChI=1S/C7H14N2/c1-6(2)8-5-9-7(3)4/h6-7H,1-4H3 N Key: BDNKZNFMNDZQMI-UHFFFAOYSA-N N InChI=1/C7H14N2/c1-6(2)8-5-9-7(3)4/h6-7H,1-4H3 Key: BDNKZNFMNDZQMI-UHFFFAOYAW
SMILES CC(C)N=C=NC(C)C
Properties
Chemical formula	C7H14N2
Molar mass	126.203 g·mol−1
Appearance	Liquid
Density	0.806 g/mL
Boiling point	145 to 148 °C (293 to 298 °F; 418 to 421 K)
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H226, H315, H317, H318, H330, H334
Precautionary statements	P210, P233, P240, P241, P242, P243, P260, P261, P264, P271, P272, P280, P284, P285, P302+P352, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P310, P312, P320, P321, P332+P313, P333+P313, P342+P311, P362, P363, P370+P378, P403+P233, P403+P235, P405, P501
Safety data sheet (SDS)	External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

N,N′-Diisopropylcarbodiimide is a carbodiimide used in peptide synthesis. As a liquid, it is easier to handle than the commonly used N,N′-dicyclohexylcarbodiimide, a waxy solid. In addition, N,N′-diisopropylurea, the byproduct of its use in many chemical reactions, is soluble in most organic solvents, a property that facilitates work-up.

Further reading

• Angell, Y (1994). "Comparative studies of the coupling of N-methylated, sterically hindered amino acids during solid-phase peptide synthesis". Tetrahedron Lett. 35 (33): 5981. doi:10.1016/0040-4039(94)88054-9.
• Izdebski, JAN; Orlowska, Alicja; Anulewicz, Romana; Witkowska, EWA; Fiertek, Dariusz (1994). "Reinvestigation of the reactions of carbodiimides with alkoxycarbonylamino acid symmetrical anhydrides : Isolation of two N-acylureas". Int. J. Pept. Protein Res. 43 (2): 184. doi:10.1111/j.1399-3011.1994.tb00521.x.