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| | Dicyclohexylcarbodiimide Basic information |
| Product Name: | Dicyclohexylcarbodiimide | | Synonyms: | N,N'-Dicyclohexylcarbodiimide [for Peptide Synthesis];N,N'-Dicyclohexylcarbodiimide, 0.1M sol.in DCM, peptide synthesis grade;N,N'-Dicyclohexylcarbodiimide, 1 M solution in dichloromethane;N,N'-Dicyclohexylcarbodiimide, 1M sol. In N-methylpyrrolidone,peptide synth.grade;N,N'-Dicyclohexylcarbodiimide,>98%;dcc solution;n,n'-dicyclohexylcarbodiimide solution;DCC Dicyclohexylcarbodiimide | | CAS: | 538-75-0 | | MF: | C13H22N2 | | MW: | 206.33 | | EINECS: | 208-704-1 | | Product Categories: | Starting Raw Materials & Intermediates;Pharmaceutical Intermediates;Amino Acid Derivatives;Biochemistry;Condensation & Active Esterification;Coupling Reactions (Peptide Synthesis);Miscellaneous;Organics;Coupling Reagent;Nucleosides, Nucleotides & Related Reagents;Peptide Synthesis;Protecting Agents, Phosphorylating Agents & Condensing Agents;Reagents for Oligosaccharide Synthesis;Synthetic Organic Chemistry;Peptide Coupling Reagents;Condensing Agents (DNA / RNA Synthesis);Peptide;Protected Amino Acids;CarbodiimidesSynthetic Reagents;Carbodiimides;Coupling;Peptide Synthesis;Synthetic Reagents;peptides;Zero-Length Crosslinker;538-75-0 | | Mol File: | 538-75-0.mol |  |
| | Dicyclohexylcarbodiimide Chemical Properties |
| Melting point | 34-35 °C(lit.) | | Boiling point | 122-124 °C6 mm Hg(lit.) | | density | 1.247 g/mL at 25 °C | | vapor pressure | 1.044-1.15Pa at 20-25℃ | | refractive index | n20/D 1.48 | | Fp | 190 °F | | storage temp. | Store below +30°C. | | solubility | methylene chloride: 0.1 g/mL, clear, colorless | | form | Waxy Solid or Crystalline Mass | | color | White to pale yellow | | Specific Gravity | 1.247 | | 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. | | InChIKey | QOSSAOTZNIDXMA-UHFFFAOYSA-N | | LogP | 5.567-6.83 at 25℃ | | CAS DataBase Reference | 538-75-0(CAS DataBase Reference) | | NIST Chemistry Reference | Methanediimine, n,n'-dicyclohexyl-(538-75-0) | | EPA Substance Registry System | Dicyclohexylcarbodiimide (538-75-0) |
| | Dicyclohexylcarbodiimide Usage And Synthesis |
| Description | Dicydohexyl carbodiimide is used in peptide chemistry
as a coupling reagent. It is both an irritant and a
sensitizer, and caused contact dermatitis in pharmacists
and chemists.
| | Chemical Properties | Colorless solid | | Chemical Properties | N,N0
-Dicyclohexylcarbodiimide (DCC) is
a white crystalline solid. Odor is sweet and heavy. | | Uses | In the synthesis of peptides. | | Uses | 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.
| | Uses | 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. | | Uses | 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. | | Definition | ChEBI: A carbodiimide compound having a cyclohexyl substituent on both nitrogen atoms. | | Preparation | A stirred mixture of N,N′-dicyclohexylurea (19.7 g), phosphorus pentoxide (100 g), sand (175 g), and pyridine (700 mL) was refluxed for 2.25 h. Stirring was no longer possible after about 30 min. The mixture was filtered and the residue was extracted with pyridine (100 mL). Pyridine was removed from the combined solutions on a flash evaporator, and the residual oil was extracted with boiling petroleum ether (bp 60–80 C°) (2 × 100 mL), and then with diethyl ether (100 mL). The combined extracts were washed with iced water (3×80 mL), dried over calcium chloride, and filtered. The solvents were removed from the filtrate under reduced pressure to give 17.4 g of an oil, which on distillation yielded 13.7 g (76%) of a clear liquid; bp 143 C° (3.5 mmHg), which solidified in the receiver; mp 34–35 C°.
Another method for producing DCC from dicyclohexylurea is a two-step process using phosphoryl chloride in dichloromethane at 40 C° for 4 h under non-basic conditions followed by removal of acidic components with aq. sodium hydroxide. This method, which gives an 89% yield of DCC, has been presented in a patent application.
 | | Preparation | Palladium acetate (22 mg, 0.1 mmol), iodine (50 mg, 0.2 mmol), and anhydrous sodium carbonate (320 mg, 3.0 mmol) were placed in a pressure vessel. Cyclohexylamine (0.11 mL, 1.0 mmol) and cyclohexyl isocyanide (0.1 mL, 0.8 mmol) were dissolved in acetonitrile (10 mL) and this solution was added to the reaction vessel, which was then pressurized with oxygen (40 psi) and heated to 100 C° for 3 h. The initially deep-red reaction mixture turned yellow-orange; no Pd black precipitation was observed. There was no obvious reaction rate dependence on oxygen pressure. The mixture was cooled to ambient temperature, depressurized, filtered, and analyzed by GC. DCC was isolated by evaporating the solvent and residual amine, followed by vacuum distillation.
Palladium(II) complexes with a carbodiimide ligand, in which a nitrogen of the linear NbCbN moiety is bonded to the metal center, and bis(carbodiimido)palladium(II) complexes, both derived from isocyanides, have been described. | | 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. | | Hazard | A poison by skin contact. Moderately toxic
by ingestion and inhalation. | | Fire Hazard | Dicyclohexylcarbodiimide is probably combustible. | | Flammability and Explosibility | Notclassified | | Contact allergens | Used in peptide chemistry as a coupling reagent. It is
both an irritant and a sensitizer and has caused contact
dermatitis in pharmacists and chemists. | | Potential Exposure | Laboratory reagent | | Shipping | UN2928 Toxic solids, corrosive, organic, n.o.s.,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials, 8-
Corrosive material, Technical Name Required. UN2811
Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-
Poisonous materials, Technical Name Required | | Purification Methods | It is sampled as a liquid after melting in warm H2O. It is sensitive to air, and it is a potent skin irritant. It can be distilled in a vacuum and is best stored in a tightly stoppered flask in a freezer. It is very soluble in CH2Cl2 and pyridine where the reaction product with H2O, after condensation, is dicyclohexyl urea which is insoluble and can be filtered off. Alternatively dissolve it in CH2Cl2, add powdered anhydrous MgSO4, shake for 4hours, filter, evaporate and distil at 0.6mm pressure and oil bath temperature of 145o. [Bodansky et al. Biochemical Preparations 10, 122 1963, Schmidt & Seefelder Justus Liebigs Ann Chem 571 83 1951, Schmidt et al. Justus Liebigs Ann Chem 612 11 1958, Beilstein 12 IV 72.] | | Incompatibilities | Dust may for explosive mixture
with air. Reacts with steam and water. N,N0
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Dicyclohexylcarbodiimide is an amine/imide: contact
with strong oxidizers may cause fire and explosions.
Incompatible with acids, strong bases, strong reducing
agents (may form flammable gasses); azo and diazo compounds (may form toxic gases); chlorinated hydrocarbons;
nitro compounds. Contact with mixture of acetic acid 1
dinitrogen trioxide may cause explosion. The combustion
of amide compounds generate nitrogen oxides (NOx).
In the presence of moisture, may attack metals and plastics. | | Waste Disposal | Whatever cannot be saved for
recovery or recycling should be managed in an appropriate
and approved waste facility. Although not a listed RCRA
hazardous waste, this material may exhibit one or more
characteristics of a hazardous waste and require appropriate
analysis to determine specific disposal requirements.
Processing, use or contamination of this product may
change the waste management options. State and local
disposal regulations may differ from federal disposal
regulations. Dispose of container and unused contents in
accordance with federal, state and local requirements |
| | Dicyclohexylcarbodiimide Preparation Products And Raw materials |
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