Premium-Grade EDC , CAS No.25952-53-8

CAS: 25952-53-8 Cat. No.: A638754 Formule: C8H18CIN3 Poids moléculaire: 191.70 Beilstein Registry Number: 5764110 Numéro CE: 247-361-2
DISPONIBLE À COMMANDE
Synonyms
1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride | 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride | EDC·HCl | EDAC·HCL | EDCI·HCl
Storage
Store at -20°C,Argon charged,Desiccated
Shipped In
Ice chest + Ice pads
★
Taille
USA
Allemagne (EU)*
Prix
Qté
5g
A638754-5g
7 En stock
—
355,90$US
25g
A638754-25g
4 En stock
—
1 182,90$US
Enter a quantity for the sizes you want to add.
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Pourquoi cette qualité

pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Store at -20°C,Argon charged,Desiccated Expédition Ice chest + Ice pads. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 5638 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Product introduction:

Premium Grade EDC is our highest quality formulation of this popular carbodiimide crosslinker, specially characterized for applications where product integrity and risk minimization are paramount.

Features of Premium Grade EDC:

• EDC—carbodiimide crosslinker for conjugation between carboxylates and amines
• High quality—identity and purity confirmed by several tests
• Product integrity—enhanced level of testing and characterization compared to standard grade
• Lot retention—ample supply of past lots retained to ensure future process testing
• Change management—Change Control Notification (CCN) service
• Consistent manufacture—batch-specific manufacturing documentation review

Compared to the standard grade product, Premium Grade EDC provides more clearly defined quality and product support by including (a) increased analytical testing and product characterization, (b) greater batch-specific information and quality assurance review, (c) extensive lot sample retention and (d) change control notification. EDC is 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride, a water-soluble carbodiimide crosslinker that activates carboxyl groups for spontaneous reaction with primary amines, enabling peptide immobilization and hapten-carrier protein conjugation. In the presence of N-hydroxysulfosuccinimide (sulfo-NHS), EDC can be used to convert carboxyl groups to amine-reactive sulfo-NHS esters. This is accomplished by mixing the EDC with a carboxyl containing molecule and adding sulfo-NHS.

Specifications of Premium Grade EDC
We manufacture crosslinking reagents to ensure the highest possible overall product integrity, consistency and performance for the intended research applications.
• Visual: White crystalline powder, free of foreign matter
• Identity: IR scan shows only peaks characteristic of EDC
• Water content: Karl Fischer titration, ≤ 2%
• Trace metals: All metals, including lead, ≤ 50 ppm
• Elemental analysis: Reported values for C, H, and N

Applications:
• Conjugate carboxyl and amino groups among peptides and proteins
• Couple haptens to immunogenic carrier proteins (e.g.,attach a peptide to KLH)
•Immobilize peptide antigens to affinity-purify antibodies
• Create NHS-activated, amine-reactive labeling compounds
• Crosslink proteins to carboxyl coated beads or surfaces
• Activate nanoparticles with amine-reactive sulfo-NHS esters

Product References:
Crosslinker Application Guide -- search for recent literature references for this product

• Reactive Moiety:Carbodiimide

• Crosslinker Type:Heterobifunctional

• Form:Solid:

• Spacer:Short(<10 Å)

• Labeling Method:Chemical Labeling

• Spacer Arm Length:0.0 Å

Spécifications

Synonymes
1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride | 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride | EDC·HCl | EDAC·HCL | EDCI·HCl
Conditions de stockage de stockage
Store at -20°C,Argon charged,Desiccated
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/528766798
Sourires canoniques
CCN=C=NCCCN(C)C.Cl
InChIKey
FPQQSJJWHUJYPU-UHFFFAOYSA-N
INCHI
1S/C8H17N3.ClH/c1-4-9-8-10-6-5-7-11(2)3;/h4-7H2,1-3H3;1H
Isomères SMILES
CCN=C=NCCCN(C)C.Cl
WGK Allemagne
3
RTECS
FF2200000
CAS alternatif
7084-11-9
Poids moléculaire
191.70
Beilstein
5764110
Reaxy-Rn
5764110
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5764110&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClasseOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Tertiary amines
Direct ParentTrialkylamines
Alternative Parents Propargyl-type 1,3-dipolar organic compounds  Carbodiimides  Organopnictogen compounds  Hydrochlorides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Tertiary aliphatic amine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbodiimide - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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4 results found

Lot NumberCertificate TypeDateArticle
A2416088A2416088Certificate of AnalysisOct 13, 2026 A638754
A2416090A2416090Certificate of AnalysisOct 13, 2026 A638754
A2416089A2416089Certificate of AnalysisJan 05, 2024 A638754
A2416091A2416091Certificate of AnalysisJan 05, 2024 A638754
Propriétés chimiques et physiques
SolubilitéSoluble in acetonitrile dichloromethane, dimethylformamide, and tetrahydrofuran. Slightly soluble in water.
SensibilitéMoisture sensitive; Heat sensitive
Point de fusion (°C)115-118°C
Poids moléculaire191.700 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass191.119 Da
Monoisotopic Mass191.119 Da
Topological Polar Surface Area28.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity134.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
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