DCC

ALDRICH/D80002 - 99%

Synonym: N,N′-Dicyclohexylcarbodiimide

CAS Number: 538-75-0
Empirical Formula (Hill Notation): C₁₃H₂₂N₂
Molecular Weight: 206.33
EC Number: 208-704-1
MDL Number: MFCD00011659
Linear Formula: C₆H₁₁N=C=NC₆H₁₁
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-D80002-25G	25 g	$26.50 1/EA	Add To Favorites
45-D80002-100G	100 g	$34.20 1/EA	Add To Favorites
45-D80002-500G	500 g	$135.00 1/EA	Add To Favorites
45-D80002-1KG	1 kg	$221.00 1/EA	Add To Favorites
45-D80002-5KG	5 kg	$955.00 1/EA	Add To Favorites

FT-NMR Spectra for N,N′-Dicyclohexylcarbodiimide solution.

This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: D80002-100G

Properties
Descriptions
Safety Info.
Basic Data

assay	99%
bp	122-124 °C/6 mmHg (lit.)
form	solid
InChI	1S/C13H22N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13H,1-10H2
InChI key	QOSSAOTZNIDXMA-UHFFFAOYSA-N
mp	34-35 °C (lit.)
Quality Level	200
reaction suitability	reaction type: Coupling Reactions
SMILES string	C1CCC(CC1)N=C=NC2CCCCC2

Application:	Carboxy group activating reagent for peptide synthesis.
Application:	DCC has been used in the preparation of titanate nanotubes-phthalocyanine(TiONts-Pc) nanohybrids and 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-yl propynoate.
Application:	DCC may be used to promote the esterification of 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-ol with propiolic acid to form 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-yl propynoate. It can also used to synthesize: • 1,3-Thiazetedine derivatives via [2+2] cycloaddition with 2-phenylethenyl- and 2-(4-nitrophenyl)ethenyl isothiocyanates. • 1,3,5-Oxadiazine-4-thiones via [4+2] cycloaddition with benzoyl isothiocyanates. • Sterically hindered 1,3,4-oxadiazole derivatives by reacting with (N-isocyanimino)triphenylphosphorane in the presence of aromatic (or heteroaromatic) carboxylic acids.
General description:	DCC is the acronym for N,N′-dicyclohexylcarbodiimide. In peptide synthesis, it is utilized for the activation of carboxyl group. The structure of DCC has been analyzed based on IR and Raman spectral data. It mediates the esterification of poly(vinyl alcohol) with free levulinic acid to form poly(vinyl alcohol-co-vinyl levulinate).
Packaging:	1 kg in poly bottle
Packaging:	25, 100, 500 g in poly bottle
Packaging:	5, 15, 18 kg in poly drum

Symbol	GHS05,GHS06
Signal word	Danger
Hazard statements	H302 - H311 - H317 - H318
Precautionary statements	P280 - P301 + P312 + P330 - P302 + P352 + P312 - P305 + P351 + P338 + P310
Hazard Codes	T
Risk Statements	22-24-41-43
Safety Statements	24-26-37/39-45
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point(F)	235.4 °F - closed cup
Flash Point(C)	113 °C - closed cup

Purity	99%
bp	122-124 °C/6 mmHg (lit.)
mp	34-35 °C (lit.)
UNSPSC	12352111

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