Thermo Scientific Chemicals

1,1'-Carbonyldiimidazole, 97%, Thermo Scientific Chemicals

Catalog number: A14688.09
10 g, Each
Thermo Scientific Chemicals

1,1'-Carbonyldiimidazole, 97%, Thermo Scientific Chemicals

Catalog number: A14688.09
10 g, Each
Quantity
Catalog number: A14688.09
also known as A14688-09
Price (EUR)
Price: 42,80
Online price: 38,52
Your price:
Quantity
-

Chemical Identifiers

CAS
530-62-1
IUPAC Name
1-(1H-imidazole-1-carbonyl)-1H-imidazole
Molecular Formula
C7H6N4O
InChI Key
PFKFTWBEEFSNDU-UHFFFAOYSA-N
SMILES
O=C(N1C=CN=C1)N1C=CN=C1
Form
Crystals or powder or crystalline powder
Assay (Non-aqueous acid-base Titration)
≥96.0 to ≤104.0% (total imidazole content)
Solution Test
5% solution in DMF is clear
Appearance (Color)
White to cream
Identification (FTIR)
Conforms

Description

Peptide 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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Peptide 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.

Solubility
Soluble in dimethylformamide.

Notes
Store in a cool place. Incompatible with water, strong acids, strong oxidizing agents, strong bases and amines.
RUO – Research Use Only

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    Safety and Handling


    Classification of the substance or mixture
    CLP classification - Regulation(EC) No 1272/2008
    Acute oral toxicity
    Category 4
    Skin Corrosion/Irritation
    Category 1
    Serious Eye Damage/Eye Irritation
    Category 1
    Reproductive Toxicity
    Category 1B
    Label Elements
    Signal Word

    Danger

    Hazard Statements

    H302 - Harmful if swallowed

    H314 - Causes severe skin burns and eye damage

    H360D - May damage the unborn child

    Precautionary Statements

    P280 - Wear protective gloves/protective clothing/eye protection/face protection

    P301 + P330 + P331 - IF SWALLOWED: Rinse mouth. Do NOT induce vomiting

    P303 + P361 + P353 - IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water or shower

    P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing

    P310 - Immediately call a POISON CENTER or doctor/physician

    Additional EU labelling

    Restricted to professional users