CAS 693-13-0

Diisopropilcarbodiimida

Descripción:

Diisopropilcarbodiimida (DIC) es un compuesto orgánico caracterizado por su grupo funcional carbodiimida, que presenta un átomo de carbono central doblemente unido a dos átomos de nitrógeno y unido por un solo enlace a dos grupos isopropilo. Es un líquido incoloro a amarillo pálido con un olor distintivo y es conocido por su papel como agente de acoplamiento en la síntesis de péptidos y otras reacciones orgánicas. DIC es altamente reactivo, particularmente con ácidos carboxílicos, facilitando la formación de amidas y ésteres a través de la activación de estos ácidos. Es soluble en disolventes orgánicos como el diclorometano y el acetonitrilo, pero es menos soluble en agua. Debido a su reactividad, DIC puede formar intermediarios estables, lo que lo hace valioso en diversas aplicaciones sintéticas. Sin embargo, debe manejarse con cuidado, ya que puede ser irritante para la piel, los ojos y el sistema respiratorio. Las precauciones de seguridad adecuadas, incluido el uso de equipo de protección personal, son esenciales al trabajar con este compuesto en entornos de laboratorio.

Fórmula: C₇H₁₄N₂

InChI: InChI=1S/C7H14N2/c1-6(2)8-5-9-7(3)4/h6-7H,1-4H3

Clave InChI: InChIKey=BDNKZNFMNDZQMI-UHFFFAOYSA-N

SMILES: C(=NC(C)C)=NC(C)C

Sinónimos:

• (E)-dipropan-2-yldiazene
• (Propan-2-yl)([[(propan-2-yl)imino]methylidene])amine
• 1,3-Diisopropylcarbodiimide
• 2-Propanamine, N,N'-methanetetraylbis-
• Carbodiimide, diisopropyl-
• Carbodimide, N,N'-Diisopropyl-
• DIC
• Diisopropyl-Carbodiimid
• Diisopropylcarbodiimide
• Dipc
• Dipcdi
• Dipci
• N,N'-Diisopropyl carbodiimide
• N,N'-Methanetetraylbis(1-methylethylamine)
• N,N'-Methanetetraylbis(2-propanamine)
• N,N'-Methantetraylbis(1-methylethylamin)
• N,N'-dipropan-2-ylcarbodiimide
• N,N'-metanotetrailbis(1-metiletilamina)
• N,N′-Diisopropylmethanediimine
• Nsc 42080
• PCI

N,N'-Diisopropylcarbodiimide

CAS: 693-13-0

Fórmula: C₇H₁₄N₂

Pureza: >98.0%(GC)

Forma y color: Colorless to Almost colorless clear liquid

Peso molecular: 126.20

Ref: 3B-D0254

N,N'-Diisopropylcarbodiimide, 99%

CAS: 693-13-0

N,N'-Diisopropylcarbodiimide is used as a reagent in synthetic organic chemistry. It serves as a chemical intermediate and as a stabilizer for Sarin (chemical weapon). It is also used in the synthesis of peptide and nucleic acid. Further, it is used as an antineoplastic and involved in the treatment

Fórmula: C₇H₁₄N₂

Pureza: 99%

Forma y color: Liquid, Clear colorless to yellow

Peso molecular: 126.20

Ref: 02-A19292

(propan-2-yl)({[(propan-2-yl)imino]methylidene})amine

CAS: 693-13-0

Fórmula: C₇H₁₄N₂

Pureza: 95%

Forma y color: Liquid

Peso molecular: 126.1995

Ref: IN-DA0035B8

N,N''-Diisopropylcarbodiimide

CAS: 693-13-0

Fórmula: C₇H₁₄N₂

Pureza: ≥ 98.5%

Forma y color: Clear, colourless to light-yellow liquid

Peso molecular: 126.20

Ref: 7W-GM2363

N,N'-Bis(isopropyl)carbodiimide

CAS: 693-13-0

N,N'-Bis(isopropyl)carbodiimide

Fórmula: C₇H₁₄N₂

Pureza: 99%

Forma y color: clear. colourless liquid

Peso molecular: 126.19946g/mol

Ref: 54-OR18304

N,N'-Diisopropylcarbodiimide

Producto controlado

CAS: 693-13-0

Applications N,N'-Diisopropylcarbodiimide can be used as an alternative to N,N’-Dicyclohexylcarbodiimide (D438500) in peptide synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Kearney, A.S., et al.: Pharm. Res., 10, 1461 (1993); Heinonen, T.M., et al.: Clin. Ther., 18, 853 (1996); Whitfield, L.R., et al.: Eur. J. Drug Metab. Pharmacokinet., 25, 97 (2000); Collingwood, S.P., et al.: Tetrahedron Lett. 28, 4445, (1987); Benoiton, N.L., et al.: J. Chem. Soc., Chem. Commun., 543, (1981)

Fórmula: C₇H₁₄N₂

Forma y color: Neat

Peso molecular: 126.2

Ref: TR-D455495

DIC

CAS: 693-13-0

DIC is a carbodiimide used as a coupling reagent for amide and ester formation, widely employed in peptide synthesis in presence of additives such as HOBt or HOAt to supress racemisation. Being a liquid, DIC is easier to handle than the solid DCC and forms a DCM-soluble urea by-product, while DCC generates a urea by-product insoluble in most organic solvents. Since the presence of insoluble urea is reportedly problematic in solid-phase peptide synthesis, for this application DIC is more suitable than DCC. A possible side-reaction with DIC and carbodiimides in general is the formation of an N-acylurea, which can be limited by conducting the reaction in DCM or chloroform at low temperatures, and by adding the amine at last.

Fórmula: C₇H₁₄N₂

Pureza: Min. 99.0%

Forma y color: Colorless Clear Liquid

Peso molecular: 126.2 g/mol

Ref: 3D-FD02073

N,N'-Diisopropylcarbodiimide

CAS: 693-13-0

Fórmula: (CH₃)₂CHNCNCH(CH₃)₂

Forma y color: colorless to light yellow liq.

Peso molecular: 126.2

Ref: 08-07-0190

1,3-Diisopropylcarbodiimide

CAS: 693-13-0

Please enquire for more information about 1,3-Diisopropylcarbodiimide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Fórmula: C₇H₁₄N₂

Pureza: Min. 99.0%

Peso molecular: 126.20 g/mol

Ref: 3D-J-670017

N,N-Diisopropyl Carbodiimide (DIPC) extrapure, 99%

CAS: 693-13-0

Fórmula: C₇H₁₄N₂

Pureza: min. 99%

Forma y color: Clear, Colourless to pale yellow to yellow, Liquid

Peso molecular: 126.20

Ref: SR-43913