03449

N-(3-dimetilaminopropil)-N′-etilcarbodiimida

≥99.0% (AT)

• Sinônimo(s): N-etil-N′-(3-dimetilaminopropil)carbodiimida, EDAC, EDC, WSC
• Fórmula empírica (Notação de Hill): C₈H₁₇N₃ · HCl
• Número CAS: 25952-53-8
• Peso molecular: 191.70
• Beilstein: 5764110
• Número CE: 247-361-2
• Número MDL: MFCD00012503
• Código UNSPSC: 12161502
• ID de substância PubChem: 329747707
• NACRES: NA.21

Propriedades

• Ensaio: ≥99.0% (AT)
• Formulário: powder
• técnica(s): bioconjugation: suitable
• pf: 110-115 °C (lit.); 112-116 °C
• solubilidade: H₂O: soluble 0.2 g/L
• temperatura de armazenamento: −20°C
• cadeia de caracteres SMILES: Cl.CCN=C=NCCCN(C)C; Cl.CCN=C=NCCCN(C)C
• InChI: 1S/C8H17N3.ClH/c1-4-9-8-10-6-5-7-11(2)3;/h4-7H2,1-3H3;1H
• chave InChI: FPQQSJJWHUJYPU-UHFFFAOYSA-N

Descrição

Descrição geral

1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride, commonly referred to as EDAC HCl, plays a pivotal role as a potent and widely utilized water-soluble reagent in chemical and biochemical research, primarily facilitating the formation of amide bonds. In the realm of peptide synthesis, EDAC HCl showcases efficiency by coupling amino acids through their carboxyl and amine groups, crucial for the creation of peptides with specific sequences and functionalities. Expanding its influence beyond peptides, EDAC HCl contributes to the construction of immunogens by covalently attaching haptens—small molecules that elicit an immune response—to carrier proteins, playing a key role in vaccine research.The versatility of EDAC HCl extends to nucleic acid modification, allowing for the labeling of DNA and RNA through their 5′ phosphate groups. This capability facilitates the visualization, tracking, and analysis of these crucial molecules, contributing significantly to advancements in nucleic acid research.

Furthermore, EDAC HCl serves as a biomolecule bridge, acting as a crosslinker that connects amine-reactive NHS-esters of biomolecules to carboxyl groups. This technique proves invaluable in protein conjugation, enabling the creation of hybrid molecules with novel properties and functions. The underlying mechanism involves EDAC HCl′s reaction with a carboxyl group, forming an unstable intermediate that actively seeks an amine partner. The delicate balance of this reaction underscores the importance of optimizing conditions for efficient conjugation. The assistance of N-hydroxysuccinimide (NHS) further enhances EDAC HCl′s capabilities by stabilizing the intermediate and enabling two-step conjugation procedures. This additional feature provides greater flexibility and control, particularly when dealing with complex biomolecules.

Aplicação

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride ≥99.0% (AT) has been used as an activator to covalently immobilize tyrosinase to prepare enzyme electrodes.[1] It has also been used as a prefixative for histamine immunolabeling.[2]

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride has been used for amine coupling reaction during self-assembly of the tethered bilayer lipid membrane.[3] It has also been used for derivatizing antibody against COX5b to carboxylated polystyrene microspheres.[4]

Ações bioquímicas/fisiológicas

Reagente de condensação solúvel em água. O EDAC, de modo geral, é utilizado como agente de ativação de grupos carboxílicos para ligação de amidas com aminas primárias. Além disso, ele reage com grupos fosfato. O EDAC foi usado, por exemplo, na síntese de peptídeos; reticulação de proteínas com ácidos nucleicos; e no preparo de imunoconjugados. Tipicamente, o EDAC é utilizado na faixa de pH de 4,0 a 6,0 sem tampões. Em particular, tampões com amina e carboxilato devem ser evitados.

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide is a water soluble condensing reagent. EDAC is generally utilized as a carboxyl activating agent for amide bonding with primary amines.[5] Additionally, it will react with phosphate groups. It has been utilized in peptide synthesis, crosslinking proteins to nucleic acids as well as preparation of immunoconjugates.[6]

Características e benefícios

Versatile and adaptable for wide variety of laboratory and research applications

Outras notas

For additional information on our range of Biochemicals, please complete this form.

Water soluble peptide coupling reagent;[7] Modification of carboxyl groups in proteins, review;[8] Synthesis of esters.[9]

Informações de segurança

• Pictogramas: GHS06,GHS08,GHS09
• Palavra indicadora: Danger
• Frases de perigo: H302,H311,H315,H317,H373,H410
• Declarações de precaução: P260 - P273 - P280 - P301 + P312 - P302 + P352 + P312 - P314
• Classificações de perigo: Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral
• Órgãos-alvo: Stomach,large intestine,lymph node
• Código de classe de armazenamento: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: dust mask type N95 (US), Eyeshields, Gloves