Sodium borohydride solution - 2.0 M in triethylene glycol dimethyl ether , CAS No.16940-66-2

CAS: 16940-66-2 Cat. No.: S432205 Fórmula: NaBH4 Peso molecular: 37.83 Número EC: 241-004-4 PubChem CID: 4311764
Disponible para pedir
CALIDAD & PUREZA 2.0 M in triethylene glycol dimethyl 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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Talla
USA
Alemania (EU)*
Precio
Cantidad
25ml
S432205-25ml
Fabricado bajo pedido · 8–12 semanas
86,90US$
100ml
S432205-100ml
2 Disponible
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265,90US$

310,90US$
Guardar 45,00 US$ (14.47%)
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Por qué esta calidad

2.0 M in triethylene glycol dimethyl ether para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

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Almacenamiento y envío

Store at 2-8°C,Argon charged Envío Wet ice,FedEx DG Service. Consulte el COA específico del lote para conocer las especificaciones exactas.

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Documentos de calidad

SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.

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Prueba documental

Citado en 3036 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Especificaciones

Sinónimos
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
Especificaciones y pureza
2.0 M in triethylene glycol dimethyl ether
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C,Argon charged
Enviado en
Wet ice,FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
[BH4-].[Na+]
IUPAC Name
sodium;boranuide
InChIKey
YOQDYZUWIQVZSF-UHFFFAOYSA-N
INCHI
1S/BH4.Na/h1H4;/q-1;+1
Isómeros SMILES
[BH4-].[Na+]
WGK Alemania
2
RTECS
ED3325000
PubChem CID
4311764
Número ONU
1426
Grupo de embalaje
I
Peso molecular
37.83

Documentación

📋 Hoja de datos de seguridad (SDS)

Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.

<<<<<<< HEAD Descargar SDS → ======= Descargar SDS → >>>>>>> release248-p3

✅ Certificado de análisis (COA)

Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.

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📊 Ficha técnica

Resumen de referencia rápida de las especificaciones y aplicaciones del producto.

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🔬 Hoja de especificaciones

Atributos de calidad completos y criterios de aceptación para esta calidad.

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Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomInorganic compounds
SuperclassMixed metal/non-metal compounds
ClaseMiscellaneous 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot NumberCertificate TypeFechaArticulo
I2622610I2622610Certificate of AnalysisOct 12, 2026 S432205
I2622624I2622624Certificate of AnalysisOct 12, 2026 S432205
G2609536G2609536Certificate of AnalysisJul 21, 2026 S432205
G2609546G2609546Certificate of AnalysisJul 21, 2026 S432205
D2624345D2624345Certificate of AnalysisMay 09, 2026 S432205
D2608214D2608214Certificate of AnalysisApr 13, 2026 S432205
A2623755A2623755Certificate of AnalysisJan 26, 2026 S432205
L2508176L2508176Certificate of AnalysisDec 10, 2025 S432205
I2518496I2518496Certificate of AnalysisSep 19, 2025 S432205
F2503572F2503572Certificate of AnalysisJun 05, 2025 S432205
L2420554L2420554Certificate of AnalysisDec 25, 2024 S432205
C2419356C2419356Certificate of AnalysisMar 30, 2024 S432205
C2404040C2404040Certificate of AnalysisMar 30, 2024 S432205
I2312654I2312654Certificate of AnalysisSep 16, 2023 S432205
E23061314E23061314Certificate of AnalysisMay 09, 2023 S432205
Propiedades químicas y físicas
SensibilidadMoisture sensitive;heat sensitive
Punto de ebullición (°C)130°C
Punto de fusión (°C)-20--10°C
Peso molecular37.840 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
Preguntas frecuentes y artículos
Professional Guide to Streptavidin-Modified Proteins
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Nanowires: Properties, Preparation Routes, and Process Selection (Comprehensive Analysis of Top-Down and Bottom-Up Approaches with Recommended Aladdin Reagents)
How to Choose a Hydrogen Evolution (HER) Catalyst: Kinetic Barriers in Water Electrolysis, AWE/PEM/AEM Pathways, and a Materials-Family Roadmap (with a Product Map)
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)
Flavones: Structural Features, Physicochemical Properties, and Key Points for Research and Applications
Glutaraldehyde-mediated Microbial Inactivation: Chemical Mechanisms, Determinants, and Key Validation Considerations
Reconsidering N-Acyl Amino Protecting Groups: Deprotection Differences, Strategic Roles, and Experimental Selection of Ac, Bz, and Tfa
Phthaloyl: Its Role in Primary Amine Protection and Practical Considerations for Experimental Selection
Research Value of Polyelectrolyte Multilayers: Layer-by-Layer Design of Interfacial Composition, Mass Transport, and Function
Experimental Selection Logic for Pentafluorophenyl-Based Systems: Practical Judgment from Active Esters and Pre-Activated Monomers to Downstream Transformations
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
Sulfonyl Hydrazide-Mediated Introduction of Small C(sp³) Fragments: Nickel-Catalyzed Cross-Coupling, Medicinal Chemistry Applications, and Reagent Selection
Thietanes: Promising Small-Ring Building Blocks with Tunable Physicochemical Properties through Sulfur Oxidation-State Control
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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