1,1'-Carbonyldiimidazole

1,1'-Carbonyldiimidazole
  • CAS No.:530-62-1
Other grades of this product :
1,1'-Carbonyldiimidazole Basic information
Product Name:1,1'-Carbonyldiimidazole
Synonyms:CARBONYLDIIMIDAZOLE;CARBODIIMIDAZOLE;LABOTEST-BB LT00233203;IM2 C O;DI(1H-IMIDAZOL-1-YL)METHANONE;CDI;(DIIMIDAZOL-1-YL)KETONE;AKOS BBS-00004316
CAS:530-62-1
MF:C7H6N4O
MW:162.15
EINECS:208-488-9
Product Categories:Zero-Length Crosslinker;blocks;AMIDE;BuildingBlocks;Peptide;pharma material;Imidazoles;Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines;Peptide Coupling Reagents;Biochemistry;Condensation & Active Esterification;Coupling Reactions (Peptide Synthesis);Heterocycles;Intermediates;Peptide Synthesis;Synthetic Organic Chemistry;530-62-1
Mol File:530-62-1.mol
1,1'-Carbonyldiimidazole Chemical Properties
Melting point 117-122 °C(lit.)
Boiling point 288.83°C (rough estimate)
density 1.303 g/mL at 25 °C
vapor pressure 0.006-0.012Pa at 20-25℃
refractive index n20/D1.434
storage temp. 2-8°C
solubility Soluble in dimethylformamide.
form Crystalline Powder
pka2.90±0.10(Predicted)
color White to light cream
PH Range7.7 at 50 g/l
PH7.7 (50g/l, H2O, 20℃)
Water Solubility Insoluble in water
Sensitive Moisture Sensitive
Merck 14,1819
BRN 6826
Stability:Stable, but moisture-sensitive. Incompatible with acids, strong oxidizing agents, water.
InChIKeyPFKFTWBEEFSNDU-UHFFFAOYSA-N
CAS DataBase Reference530-62-1(CAS DataBase Reference)
EPA Substance Registry System1H-Imidazole, 1,1'-carbonylbis- (530-62-1)
Safety Information
Hazard Codes C,Xi,Xn
Risk Statements 22-34-36/37/38-40-36/38
Safety Statements 26-36/37/39-45-37/39-27-36/37
RIDADR UN 3263 8/PG 2
WGK Germany 2
10-21
Hazard Note Harmful/Corrosive/Moisture Sensitive
TSCA T
HazardClass 8
PackingGroup III
HS Code 29332990
ToxicityLD50 orally in Rabbit: 1071 mg/kg
MSDS Information
ProviderLanguage
1,1'-Carbonyldiimidazole English
ACROS English
SigmaAldrich English
ALFA English
1,1'-Carbonyldiimidazole Usage And Synthesis
Chemical PropertiesWhite crystalline powder
UsesUsed in the synthesis of peptides. Contains up to 10% imidazole.
Usespeptide coupling reagent
UsesCDI is mainly employed to convert alcohols and amines into carbamates, esters, and ureas. It is also used in the synthesis of peptides and nucleoside triphosphates.
Uses1,1'-Carbonyldiimidazole is a peptide coupling reagent,it is used in the synthesis of peptides. Reacts readily with carboxylic acids to form acyl imidazoles; subsequent reaction with amines to form amides goes smoothly.
UsesPeptide coupling reagent1,1'-Carbonyldiimidazole acts as a coupling reagent and utilized for coupling of amino acids in order to prepare peptide in organic synthesis. It is also used in the preparation of beta-keto sulfones, sulfoxides and beta-enamino acid derivatives. It is used to convert alcohols and amines into carbamates, esters, and ureas. It is involved in the preparation of formylized imidazole by reaction with formic acid. Further, it is used in the synthesis of dipolar polyamides compounds. In addition to this, it is considered as an equivalent of phosgene and used to prepare asymmetric bis alkyl carbonate.
General Description1,1′-Carbonyldiimidazole (N,N′-carbonyldiimidazole) is a versatile peptide-forming reagent.
Purification MethodsCrystallise it from *benzene or tetrahydrofuran in a dry-box and store it dry. [Hearn Methods Enzymol 135 102 1987, Beilstein 23/4 V 245.]

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