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DIC (N,N′-diisopropylcarbodiimide) Chemicals Molecular Depot
DIC (N,N′-diisopropylcarbodiimide) Chemicals Molecular Depot

DIC (N,N′-diisopropylcarbodiimide)

$907.00

    Catalog Number: B2015766 (5 mL)

    DIC (N,N′-diisopropylcarbodiimide) is a high quality carbodiimide used as a coupling reagent in the synthesis of amides, peptides, ureas, heterocycles, and unsymmetrical carbodiimides. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

    Products are for in vitro research use only (RUO).

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DIC (N,N′-diisopropylcarbodiimide) – Catalog Number: B2015766 (5 mL)

Catalog number: B2015766
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 5 mL
Molecular Weight or Concentration: 126.2
Supplied as: Solution
Applications: a molecular tool for various biochemical applications
Storage: RT
Keywords: N,N′-Diisopropylcarbodiimide
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

DIC (N,N′-diisopropylcarbodiimide) is supplied as a biotechnology-grade solution in a defined 5 mL fill (Catalog B2015766) with storage at RT. The supplier identifies this reagent as a high-quality carbodiimide used as a coupling reagent in the synthesis of amides, peptides, ureas, heterocycles, and unsymmetrical carbodiimides. It is also noted as a molecular tool for various biochemical applications and has been used in a wide array of other chemical and immunological workflows. These concise, documentation-friendly fields—amount, supplied-as, storage, keyword identity, and a biotechnology-grade statement—support straightforward SOP inclusion and inventory traceability for multi-user labs.

In research practice, carbodiimide coupling reagents are valued for activating carboxyl groups toward bond formation with nucleophiles under mild conditions. A liquid presentation allows direct volumetric dosing and rapid compatibility checks with intended solvent systems. Because no working concentration or protocol is prescribed on the listing, good bench practice is to determine conditions empirically for the matrix and functional groups at hand. Pilot titrations that vary reagent equivalents, solvent composition, and temperature, with careful documentation of times and quench/cleanup steps, help establish a reliable operating window. Recording lot identifiers and time-at-temperature provides reproducibility across operators and batches and simplifies transfer into formal SOPs.

Typical use-cases include assembling qualitative coupling controls for method development, drafting training exercises that demonstrate carbodiimide-mediated activation, and running small-scale screens to compare coupling strategies in peptide or urea formation. The supplier’s emphasis on broad applicability across chemical, biochemical, and immunological contexts aligns with these scenarios, and the ready-to-use solution format integrates easily into benchtop workflows. Within research-only boundaries, this DIC offering provides a clearly specified, dependable component for laboratories standardizing carbodiimide-based coupling and exploratory synthesis.

Why researchers choose this product:

  • Identified by the supplier as a coupling reagent for amides, peptides, ureas, heterocycles, and unsymmetrical carbodiimides
  • Ready-to-use solution format in a defined 5 mL fill supports quick method setup
  • Listed use across biochemical, chemical, and immunological workflows
  • Specified RT storage simplifies routine handling and inventory
  • Biotechnology-grade note supports low-background expectations during optimization

This product is for Research Use Only (RUO). It is not intended for diagnostic or therapeutic use.

References

  • 1: Budischowsky D, Sulaeva I, Hettegger H, Ludwig R, Rosenau T, Potthast A. Fluorescence labeling of C1-oxidized cellulose. Part 1: Method development Carbohydr Polym. 2022 Nov 1;295:119860.
  • 2: Kawashima H, Sohma Y, Nakanishi T, Kitamura H, Mukai H, Yamashita M, Akaji K, Kiso Y. A new class of aggregation inhibitor of amyloid-β peptide based on an O-acyl isopeptide Bioorg Med Chem. 2013 Nov 1;21(21):6323-7.
  • 3: Lüttenberg S, Sondermann F, Scherkenbeck J. Anthelmintic PF1022A: stepwise solid-phase synthesis of a cyclodepsipeptide containing N-methyl amino acids Tetrahedron. 2012 Feb 25;68(8):2068-2073.
  • 4: Surh I, Behl M, Elmore SA, Chhabra RS. Comparative dermal toxicity of dicyclohexylcarbodiimide and diisopropylcarbodiimide in rodents Cutan Ocul Toxicol. 2012 Sep;31(3):177-87.
  • 5: National Toxicology Program. Toxicology and carcinogenesis studies of diisopropylcarbodiimide (Cas No. 693-13-0) in F344/N rats and B6C3F1 mice (dermal studies) Natl Toxicol Program Tech Rep Ser. 2007 Feb;(523):1-286.
  • 6: Hayes BB, Gerber PC, Griffey SS, Meade BJ. Contact hypersensitivity to dicyclohexylcarbodiimide and diisopropylcarbodiimide in female B6C3F1 mice Drug Chem Toxicol. 1998 May;21(2):195-206.
  • 7: Baktır Z, Akkurt M, Kandinska MI, Bogdanov MG, Büyükgüngör O. (S)-Methyl 2-[(3R,4R)-2-benzyl-3-(2-fur-yl)-1-oxo-1,2,3,4-tetra-hydro-isoquinoline-4-carboxamido]-3-(1H-indol-3-yl)propanoate Acta Crystallogr Sect E Struct Rep Online. 2009 Jun 6;65(Pt 7):o1461-2.
  • 8: Witt KL, Tice RR, Shelby MD, Chhabra RS, Zeiger E. Induction of micronucleated erythrocytes in rodents by diisopropylcarbodiimide and dicyclohexylcarbodiimide: dependence on exposure protocol Environ Mol Mutagen. 1999;33(1):65-74.
  • 9: Hicks J, Mansikkamäki A, Vasko P, Goicoechea JM, Aldridge S. A nucleophilic gold complex Nat Chem. 2019 Mar;11(3):237-241.
  • 10: Liu B, Yang Y, Cui D, Tang T, Chen X, Jing X. C-H activation motivated by N,N’-diisopropylcarbodiimide within a lutetium complex stabilized by an amino-phosphine ligand Dalton Trans. 2007 Oct 10;(38):4252-4. pubmed.ncbi.nlm.nih.gov

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FeatureDetails
Viewing Head Siedentopf type trinocular head, inclined at 30°, Interpupillary adjustment 53mm to 75mm, graduated diopter on left eyetube (30mm I.D. eyetubes)
Eyepieces SWH10X Widefield high eyepoint eyepiece, Field No. 22, tube O.D. 30.0 mm
Nosepiece Quintuple
Quintuple LWD Planachromat Phase 10x, 20x
Condenser TC Condenser N.A. 0.30, W.D. 73.0mm
Stage180mm(X) x 245mm(Y) plain stage with replaceable glass insert with 45mm opening, Glass Stage plate insert
IlluminationKoehler without iris, with phase slider, 3W LED
WarrantyLIMITED LIFETIME WARRANTY

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