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DCC

SIAL/36650 - puriss., ≥99.0% (GC)

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 Quantity
45-36650-100G 100 g
$91.70
1/EA
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45-36650-500G 500 g
$156.00
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45-36650-2.5KG 2.5 kg
$352.00
1/EA
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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: 36650-100G
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: 36650-500G
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: 36650-2.5KG

 

application(s) peptide synthesis
assay ≥99.0% (GC)
bp 122-124 °C/6 mmHg (lit.)
form solid
grade puriss.
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 32.0-37.0 °C
  34-35 °C (lit.)
Quality Level 200 
reaction suitability reaction type: Coupling Reactions
SMILES string C1CCC(CC1)N=C=NC2CCCCC2
solubility methylene chloride: 0.1 g/mL, clear, colorless
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 may be 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 the presence of aromatic (or heteroaromatic) carboxylic acids.

General description: DCC is an organic compound widely used as a coupling reagent in peptide synthesis. It is also employed as an efficient dehydrating agent for the preparation of amides, esters, nitriles, and anhydrides. Alcohols can be converted into aldehydes and ketone by Moffatt oxidation reaction in the presence of DCC and dimethyl sulfoxide (DMSO).
Other Notes: Coupling reagent, reagent for dehydrations etc. Modifies bovine heart mitochondrial transhydrogenase; Inhibition of F1F0-ATPase and other proton-translocating enzymes
Packaging: 100, 500 g in poly bottle
Packaging: 2.5 kg in poly bottle
Purity ≥99.0% (GC)
bp 122-124 °C/6 mmHg (lit.)
mp 32.0-37.0 °C; 34-35 °C (lit.)
UNSPSC 12352000

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