Benzamidine - Moligand™, ≥95% , CAS No.618-39-3

CAS: 618-39-3 Cat. No.: B349126 Formule: C7H8N2 Poids moléculaire: 120.15 Numéro CE: 210-546-3
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥95%
Synonyms
A852076 | AB01943 | Q4890748 | DTXSID8045012 | HMS3370L08 | 1ce5 | 1bra | 1f5k | 1v2s | NCGC00015160-05 | 64F5C29D-34E7-4815-B5F3-CC94EA3D2CAD | NSC243704 | NSC-243704 | 1c5z | 1v2j | 1v2v | 2j9n | Benzamidine (Protonated) | AKOS000201384 | Lopac-B-6506 |
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Taille
USA
Allemagne (EU)*
Prix
Qté
250mg
B349126-250mg
1 En stock
—
16,90$US
1g
B349126-1g
2 En stock
—
45,90$US
5g
B349126-5g
2 En stock
—
149,90$US
10g
B349126-10g
2 En stock
—
229,90$US
Enter a quantity for the sizes you want to add.
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Pourquoi cette qualité

Moligand™, ≥95% Moligand™ 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 2-8°C,Argon charged Expédition Wet ice. 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 3 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Benzamidine was used in the preparation of heparan sulfate-rich proteoglycan from mouse mammary epithelial cells. It has been used to prevent enzymatic degradation during the purification procedure of bovine factor XII (Hageman factor).

Spécifications

Synonymes
A852076 | AB01943 | Q4890748 | DTXSID8045012 | HMS3370L08 | 1ce5 | 1bra | 1f5k | 1v2s | NCGC00015160-05 | 64F5C29D-34E7-4815-B5F3-CC94EA3D2CAD | NSC243704 | NSC-243704 | 1c5z | 1v2j | 1v2v | 2j9n | Benzamidine (Protonated) | AKOS000201384 | Lopac-B-6506 |
Spécifications et pureté
Moligand™, ≥95%
Mécanismes biochimiques et physiologiques
Benzamidine is an inhibitor of plasmin and has been used in the radioimmunoassay of glucagon in human plasma. It prevents the destruction of Thyrotropin-releasing hormone (TRH) added to whole blood in vitro before radioimmunoassay of TRH.
Conditions de stockage de stockage
Store at 2-8°C,Argon charged
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Moligand™
Pureté
≥95%
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504750557
Sourires canoniques
C1=CC=C(C=C1)C(=N)N
IUPAC Name
benzenecarboximidamide
InChIKey
PXXJHWLDUBFPOL-UHFFFAOYSA-N
INCHI
1S/C7H8N2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H3,8,9)
Isomères SMILES
C1=CC=C(C=C1)C(=N)N
WGK Allemagne
3
Poids moléculaire
120.15
Reaxy-Rn
606020
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606020&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.

Voir la fiche technique →

🔬 Fiche de spécifications

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

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Carboximidamides  Carboxamidines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Carboximidamide - Carboxylic acid amidine - Amidine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors carboxamidine - benzenes
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
F10 Tclin Coagulation factor X (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
F2 Tclin Prothrombin (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLG Tclin Plasminogen (2339 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRSS1 Tclin Trypsin I (2306 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F10 Tclin Coagulation factor X (9693 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRSS2 Tchem Trypsin II (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ARSA Tbio Cerebroside-sulfatase (655 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLAT Tclin Tissue-type plasminogen activator (1057 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLAU Tchem Urokinase-type plasminogen activator (2016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACR Tchem Acrosin (277 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AOX1 Tchem Aldehyde oxidase (429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ST14 Tchem Matriptase (677 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F7 Tchem Coagulation factor VII/tissue factor (740 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
Trypsin (394 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sus scrofa (849 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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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24 results found

Lot NumberCertificate TypeDateArticle
J2629237J2629237Certificate of AnalysisOct 17, 2026 B349126
J2629236J2629236Certificate of AnalysisOct 17, 2026 B349126
J2629235J2629235Certificate of AnalysisOct 17, 2026 B349126
J2629234J2629234Certificate of AnalysisOct 17, 2026 B349126
D2614389D2614389Certificate of AnalysisMar 13, 2026 B349126
D2614391D2614391Certificate of AnalysisMar 13, 2026 B349126
D2614396D2614396Certificate of AnalysisMar 13, 2026 B349126
D2614397D2614397Certificate of AnalysisMar 13, 2026 B349126
A2614260A2614260Certificate of AnalysisDec 29, 2025 B349126
A2614261A2614261Certificate of AnalysisDec 29, 2025 B349126
A2614262A2614262Certificate of AnalysisDec 29, 2025 B349126
A2614259A2614259Certificate of AnalysisDec 29, 2025 B349126
K2528109K2528109Certificate of AnalysisDec 09, 2025 B349126
H2514233H2514233Certificate of AnalysisAug 06, 2025 B349126
H2514234H2514234Certificate of AnalysisAug 06, 2025 B349126
H2514232H2514232Certificate of AnalysisAug 06, 2025 B349126
H2514231H2514231Certificate of AnalysisAug 06, 2025 B349126
G2431147G2431147Certificate of AnalysisJul 18, 2024 B349126
G2431146G2431146Certificate of AnalysisJul 18, 2024 B349126
G2431145G2431145Certificate of AnalysisJul 18, 2024 B349126
K2201215K2201215Certificate of AnalysisAug 05, 2022 B349126
K2201216K2201216Certificate of AnalysisAug 05, 2022 B349126
K2201299K2201299Certificate of AnalysisAug 05, 2022 B349126
K2201335K2201335Certificate of AnalysisAug 05, 2022 B349126
Propriétés chimiques et physiques
SensibilitéAir sensitive
Point d'éclair (°C)79.9ºC
Point d'ébullition (°C)~208.5° C at 760 mmHg (Predicted)
Point de fusion (°C)42.90° C (Predicted)
Poids moléculaire120.150 g/mol
XLogP30.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass120.069 Da
Monoisotopic Mass120.069 Da
Topological Polar Surface Area49.900 Ų
Heavy Atom Count9
Formal Charge0
Complexity103.000
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 Count1
FAQ et articles
Citations of This Product
Calculateurs de solution
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