Sodium borohydride solution - 0.5 M in 2-methoxyethyl ether , CAS No.16940-66-2

CAS: 16940-66-2 Cat. No.: S432204 Formule: NaBH4 Poids moléculaire: 37.83 Numéro CE: 241-004-4 PubChem CID: 4311764
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ 0.5 M in 2-methoxyethyl ether
Synonyms
BORATE(1-), TETRAHYDRO-, SODIUM (1:1) | EINECS 241-004-4 | sodium;boranuide | O0577 | COLORSTRIP 2000 | sodium boro hydride | sodium boranuide | SODIUM TETRAHYDRIDOBORATE | 87L0B9CPPA | sodium borohydri- de | sodium borohydrid | EC 241-004-4 | NaBH | natr
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice,FedEx DG Service
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Taille
Allemagne (EU)
USA*
Prix
Qté
100ml
S432204-100ml
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137,88€

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Pourquoi cette qualité

0.5 M in 2-methoxyethyl ether 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,FedEx DG Service. 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 3036 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes
BORATE(1-), TETRAHYDRO-, SODIUM (1:1) | EINECS 241-004-4 | sodium;boranuide | O0577 | COLORSTRIP 2000 | sodium boro hydride | sodium boranuide | SODIUM TETRAHYDRIDOBORATE | 87L0B9CPPA | sodium borohydri- de | sodium borohydrid | EC 241-004-4 | NaBH | natr
Spécifications et pureté
0.5 M in 2-methoxyethyl ether
Conditions de stockage de stockage
Store at 2-8°C,Argon charged
Expédié en
Wet ice,FedEx DG Service
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants
Pubchem Sid
Sourires canoniques
[BH4-].[Na+]
IUPAC Name
sodium;boranuide
InChIKey
YOQDYZUWIQVZSF-UHFFFAOYSA-N
INCHI
1S/BH4.Na/h1H4;/q-1;+1
Isomères SMILES
[BH4-].[Na+]
WGK Allemagne
2
RTECS
ED3325000
PubChem CID
4311764
Numéro ONU
1426
Groupe d'emballage
I
Poids moléculaire
37.83

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.

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📊 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

KingdomInorganic compounds
SuperclassMixed metal/non-metal compounds
ClasseMiscellaneous mixed metal/non-metals
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentMiscellaneous mixed metal/non-metals
Alternative Parents Metalloid salts  Inorganic sodium salts  
Molecular FrameworkNot available
Substituents Inorganic sodium salt - Inorganic salt - Miscellaneous mixed metal/non-metal - Inorganic metalloid salt
DescriptionThis compound belongs to the class of inorganic compounds known as miscellaneous mixed metal/non-metals. These are inorganic compounds containing non-metal as well as metal atoms but not belonging to afore mentioned classes.
External Descriptors inorganic sodium salt - metal tetrahydridoborate
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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16 results found

Lot NumberCertificate TypeDateArticle
I2601866I2601866Certificate of AnalysisSep 12, 2026 S432204
E2626484E2626484Certificate of AnalysisJun 04, 2026 S432204
C2611662C2611662Certificate of AnalysisApr 02, 2026 S432204
L2508746L2508746Certificate of AnalysisDec 12, 2025 S432204
K2518547K2518547Certificate of AnalysisNov 22, 2025 S432204
H2528618H2528618Certificate of AnalysisSep 09, 2025 S432204
G2508695G2508695Certificate of AnalysisJul 16, 2025 S432204
D2525451D2525451Certificate of AnalysisMay 06, 2025 S432204
A2515418A2515418Certificate of AnalysisFeb 07, 2025 S432204
I2426354I2426354Certificate of AnalysisSep 30, 2024 S432204
E2406215E2406215Certificate of AnalysisJun 05, 2024 S432204
A2424281A2424281Certificate of AnalysisJan 26, 2024 S432204
H23031139H23031139Certificate of AnalysisAug 23, 2023 S432204
H23031151H23031151Certificate of AnalysisAug 23, 2023 S432204
G23041102G23041102Certificate of AnalysisJul 07, 2023 S432204
G23041103G23041103Certificate of AnalysisJul 07, 2023 S432204
Propriétés chimiques et physiques
SensibilitéMoisture,Heat sensitive
Point d'ébullition (°C)130°C
Point de fusion (°C)-20--10°C
Poids moléculaire37.840 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass38.0304 Da
Monoisotopic Mass38.0304 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count2
Formal Charge0
Complexity2.000
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
FAQ et articles
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Installing a Redox Switch on Biomolecules: Principles, Conjugation Essentials, and an Application Guide for ATTO MB2 NHS ester
Selection of Common Research Salts: A Task Map for Alkali Metal Salts & Alkaline Earth Metal Salts (with Product Tables 1–6)
Why Metal Nanocatalysts Can “Save Energy Yet Lose Performance Easily”: Durability Logic from Active Sites to Support/Interface Engineering (Including Selection Guide and Product Tables A–D)
2-Methylpyridine–Borane (2-Picoline·BH₃) Reductive Amination Guide: Process Drivers for Replacing NaBH₃CN, the Practical Operating Window, and Scale-Up/Quench Close-Out Essentials (Including Product Tables 1–3)
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Reaction Selection in Small-Molecule Synthesis: From Transformation-Type Assessment to Experimental Route Screening
Application Differences Among Glutaraldehyde, Paraformaldehyde, and Formalin in Tissue and Cell Sample Fixation
Practical Guide to TSA Tyramide Signal Amplification: How to Select Reagents, Optimize the Workflow, and Reduce Background When Detection Signals Are Weak for Low-Abundance Targets
From Diverse Ketones to Three-Dimensional Spirocyclic Building Blocks: Reaction Design of [1.1.1]Propellane-Involved Ketone Ring Expansion
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Skin Mechanism of Action of Pro-Xylane: From C-Xyloside Priming and CS/DS Chain Remodeling to the Dermal–Epidermal Junction
Design Logic of Fluorinated 3,3-Disubstituted Oxetane Building Blocks: Structural Construction and Modulation of Amine Basicity, Lipophilicity, and Metabolic Stability
Build the Three-Membered Ring First, or Form the Carbon–Nitrogen Bond First?—Retrosynthetic Strategies, Route Selection, and Stereochemical Control in Cyclopropylamine Synthesis
Route Selection for Thiol Synthesis: C–S Bond Construction, Sulfur Source Forms, and Thiol Release
ACT-1014-6470 Kilogram-Scale Synthesis: N7-Selective Reductive Amination of an Unprotected Pyrazole, Subsequent N2 Alkylation, and Intramolecular Urea Formation
MTAD-Mediated Oxidative Dearomatization of Pyridines: Transient para-Cycloaddition, Alkene Oxidation, and Heteroatom Functionalization
Citations of This Product
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