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Dicyclohexylcarbodiimide

CAS No.538-75-0
Chemical Name:Dicyclohexylcarbodiimide
Synonyms:DCC;DCCI;DCCD;DCC/DCCI;NSC 30022;NSC 53373;NSC 57182;Dicyclimide;dcc solution;N,N-二环己基羰二亚胺(DCC)
CBNumber:CB9706578
Molecular Formula:C13H22N2
Formula Weight:206.33
MOL File:538-75-0.mol
Dicyclohexylcarbodiimide Property
mp : 34-35 °C(lit.)
bp : 122-124 °C6 mm Hg(lit.)
density : 1.247 g/mL at 25 °C
refractive index : n20/D 1.48
Fp : 190 °F
storage temp. : Store at RT.
solubility : methylene chloride: 0.1 g/mL, clear, colorless
Water Solubility : Reaction
Sensitive : Moisture Sensitive
Merck : 14,3096
BRN : 610662
Stability:: Stable, but moisture sensitive. Combustible. Incompatible with strong oxidizing agents. Avoid exposure to air or moisture.
CAS DataBase Reference: 538-75-0(CAS DataBase Reference)
NIST Chemistry Reference: Methanediimine, n,n'-dicyclohexyl-(538-75-0)
EPA Substance Registry System: Cyclohexanamine, N,N'-methanetetraylbis- (538-75-0)
Safety
Hazard Codes : T,Xn,T+
Risk Statements : 23/24/25-34-40-43-41-36/38-21-24-22-62-37/38-10-61-26-38-20/22
Safety Statements : 26-36/37/39-45-41-24-37/39-24/25-36-16-53-28
RIDADR : UN 2922 8/PG 2
WGK Germany : 3
RTECS : FF2160000
F : 3-8-10-21
HazardClass : 6.1
PackingGroup : II
HS Code : 29252000

Dicyclohexylcarbodiimide Chemical Properties,Usage,Production

Chemical Properties
Colorless solid
Usage
This product is mainly used in amikacin, glutathione dehydrants, as well as in synthesis of acid anhydride, aldehyde, ketone, isocyanate; when it is used as dehydrating condensing agent, it reacts to dicyclohexylurea through short-time reaction under normal temperature. This product can also be used in synthesis of peptide and nucleic acid. It is easy to use this product to react with compound of free carboxy and amino-group into peptide. This product is widely used in medical, health, make-up and biological products, and other synthetic fields.
Usage
N,N'-Dicyclohexylcarbodiimide is a carbodiimide used to couple amino acids during peptide synthesis. N,N'-Dicyclohexylcarbodiimide is used as a dehydrating agent for the preparation of amides, ketones , nitriles as well as in the inversion and esterification of secondary alcohols.
Usage
dicyclohexylcarbodiimide is used as a dehydrating agent at room temperature after a short reaction time, after the reaction product is dicyclohexylurea. the product is very small solubility in an organic solvent, so that easy separation of the reaction product.
General Description
White crystalline solid with a heavy sweet odor.
Air & Water Reactions
Sensitive to moisture.
Reactivity Profile
Dicyclohexylcarbodiimide is an imide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). Dicyclohexylcarbodiimide is incompatible with acids and oxidizing agents. Dicyclohexylcarbodiimide reacts with water.
Fire Hazard
Dicyclohexylcarbodiimide is probably combustible.
Dicyclohexylcarbodiimide Preparation Products And Raw materials
Raw materials
N,N'-DICYCLOHEXYLUREA Urea Carbon disulphide DCHA Cyclohexylamine Azabenzene 1,3-Dicyclohexylthiourea
Preparation Products
Benexate Hydrochloride ANGIOTENSIN II, HUMAN NAPHTHOL AS-BI PHOSPHATE IBUTILIDE Docetaxel Latanoprost Enalapril H-BETA-ALA-OTBU HCL Octreotide acetate 7-DIETHYLAMINO-3-THENOYLCOUMARIN 2,6-DICHLOROPHENETHYLISOCYANIDE TERT-BUTYL 3-HYDROXYPROPIONATE 2-MORPHOLINOISONICOTINALDEHYDE Cefprozil hydrate Lisinopril GLY-7-AMINO-4-METHYLCOUMARIN 4-ISOCYANOBENZOPHENONE Paroxetine Captopril 2-CYANOPYRIDINE-4-CARBOXALDEHYDE 7-(((2-Amino-4-thiazolyl)(methoxyimino)acetyl)amino)-3-(((5-(carboxymethyl)-4-methyl-2-thiazolyl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid 1-(2-ISOCYANO-ETHYL)-4-METHYL-PIPERAZINE (S)-3-Aminoquinuclidine dihydrochloride 1-[[(6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)[(1-carboxy-1-methylethoxy)imino] acetyl] amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0] oct-2-en-3-yl]methyl]pyridinum hydroxide inner salt 3-CARBETHOXY-4-HYDROXYCOUMARIN TERT-BUTYL METHYL MALONATE Isobutyric anhydride Trandolapril Beraprost Cyclic AMP Tetrabenzyl pyrophosphate
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DNA / RNA Synthesis Condensation & Active Esterification Coupling Reactions (Peptide Synthesis) Reagents for Oligosaccharide Synthesis Peptide Synthesis Condensing Agents (DNA / RNA Synthesis) Synthetic Reagents Coupling Carbodicyclohexylimide Carbodiimide, dicyclohexyl- Dicyclimide dicyclohexyl-carbodiimid n,n’-dicyclohexylcarbodiimide,1msol.inn-methylpyrrolidone,peptidesynthesisgrade n,n’-methanetetraylbis-cyclohexaamin n,n’-methanetetraylbis-cyclohexanamin N,N’-methanetetraylbis-Cyclohexanamine n,ni-dicyclohexylcarbodiimide N,N'-Methanetetraylbiscyclohexanamine N,N'-DICYLOHEXYLCARBODIIMIDE N,N-DICYCHOHEXYLCARBODIIMIDE N,N-DICYCLOHEXYL CARBODIIMIDE N,N'-DICYCLOHEXYLCARBODIIMIDE Carbodiimides 1,3-DICYCLOHEXYLCARBODIIMIDE 538-75-0 Bis(cyclohexyl)carbodiimide DCCI DCC DCCD CYCLOHEXANAMINE, N,N'-METHANETETRAYLBIS- DICYCLOHEXYLCARBODIIMIDE DICYCLOHEXYLCARBOXIMIDE(1,3-) N'N-dicyclohexylcarbodiimide(DCC) 1,3-DICYCLOHEXYLCARBODIIMIDE, 1.0M SOLUT ION IN DICHLOROMETHANE N,N-DICYCLOHEXYLCARBODIIMIDE SOLUTION, ~1 M IN NMP N,N'-DICYCLOHEXYLCARBODIIMIDE SOL. ~1 M IN DICHLOROMETHANE DCC (N, N'-Dicyclohexylcarbodiimide N,N-Dicyclohexylcarbodiimide99% N,N'DicyclohexylcarbodimideForSynthesis DCC (N,N-dichyclohexylcarbodiimide) N,N'-Dicyclohexylcarbodiimide, 0.1M sol.in DCM, peptide synthesis grade C13H22N2 N,N'-Dicyclohexylcarbodiimide, 1 M solution in dichloromethane N,N'-Dicyclohexylcarbodiimide, 1M sol. In N-methylpyrrolidone,peptide synth.grade N,N'-Dicyclohexylcarbodiimide,>98% 537-75-0 dcc solution n,n'-dicyclohexylcarbodiimide solution DCC Dicyclohexylcarbodiimide DCC N,N''-DICYCLOHEXYLCARBODIMIDE C6H11NCNC6H11 Pharmaceutical Intermediates Amino Acid Derivatives Starting Raw Materials & Intermediates N,N''-DICYCLOHHEXYLCARBODIIMIDE 438-75-0 Miscellaneous Organics
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