Sodium bicarbonate - PrimorTrace™, ≥99.99% metals basis , CAS No.144-55-8

CAS: 144-55-8 Cat. No.: S401669 Fórmula: NaHCO3 Peso molecular: 84.01 Beilstein Registry Number: 4153970 Número EC: 205-633-8
Disponible para pedir
CALIDAD & PUREZA PrimorTrace™ ? PrimorTrace™ — Aladdin's trace-metal-analysis line with ultra-low metal background. Use for ICP/AAS trace-metal work where contamination must be minimal. ≥99.99% metals basis
Synonyms
Baking soda | SODIUM BICARBONATE [USP MONOGRAPH] | SODIUM BICARBONATE COMPONENT OF NORMOCARB | Sodium bicarbonate in plastic container | Acidosan | Natrii hydrogencarbonas | Natrum bicarbonicum | Neut (TN) | PF 573228 pound>>PF573228 | Sodium bicarbonate
Storage
Argon charged,Room temperature
Shipped In
Normal
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
100g
S401669-100g
2 Disponible
2 Disponible
22,90US$
500g
S401669-500g
Disponible ≥10
7 Disponible

58,90US$

68,90US$
Guardar 10,00 US$ (14.51%)
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Por qué esta calidad

PrimorTrace™, ≥99.99% metals basis PrimorTrace™ para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

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Almacenamiento y envío

Argon charged,Room temperature Envío Normal. 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 1650 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Descripción general

Sodium bicarbonate is a commonly used laboratory chemical. The compound can react with both acids and bases, therefore it can be used as a neutralizer. When reacting with bases the compound forms carbonates. Sodium bicarbonate may be used to remove or wash acidic impurities from a crude liquid to yield a purer sample. Sodium bicarbonate reacts with the carboxyl groups to give a fast-forming and effervescent CO2 formation which has been used to test for the presence of carboxylic groups in proteins. Sodium bicarbonate has been observed to significantly decrease serum potassium levels as well as increase blood pH and bicarbonate concentration. The compound has been recorded to decrease the duration of peripheral nerve block in rats when when added to Lidocaine.
A commonly used laboratory pH neutralizer that reacts with acids and bases.

Especificaciones

Sinónimos
Baking soda | SODIUM BICARBONATE [USP MONOGRAPH] | SODIUM BICARBONATE COMPONENT OF NORMOCARB | Sodium bicarbonate in plastic container | Acidosan | Natrii hydrogencarbonas | Natrum bicarbonicum | Neut (TN) | PF 573228 pound>>PF573228 | Sodium bicarbonate
Especificaciones y pureza
PrimorTrace™, ≥99.99% metals basis
Condiciones de almacenamiento de almacenamiento
Argon charged,Room temperature
Enviado en
Normal
Grado
PrimorTrace™
Pureza
≥99.99% metals basis
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
C(=O)(O)[O-].[Na+]
IUPAC Name
sodium;hydrogen carbonate
InChIKey
UIIMBOGNXHQVGW-UHFFFAOYSA-M
INCHI
1S/CH2O3.Na/c2-1(3)4;/h(H2,2,3,4);/q;+1/p-1
Isómeros SMILES
C(=O)(O)[O-].[Na+]
RTECS
VZ0950000
CAS alternativo
144-55-8,7542-12-3 (unspecified hydrochloride salt)
Términos de entrada MeSH
Baking Soda;Bicarbonate, Sodium;Carbonic Acid Monosodium Salt;Hydrogen Carbonate, Sodium;Soda, Baking;Sodium Bicarbonate;Sodium Hydrogen Carbonate
Peso molecular
84.01
Beilstein
4153970

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

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Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseOrganic carbonic acids and derivatives
SubclassOrganic carbonic acids
Intermediate Tree Nodes Not available
Direct ParentOrganic carbonic acids
Alternative Parents Carbonate salts  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Carbonate salt - Carbonic acid - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as organic carbonic acids. These are compounds comprising the carbonic acid functional group.
External Descriptors one-carbon compound - organic sodium salt
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase V (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colletotrichum musae (107 Activities)
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Trypanosoma cruzi (99888 Activities)
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Fusarium verticillioides (912 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Lasiodiplodia theobromae (193 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Venturia inaequalis (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Astrosclerin-3 (80 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Malus domestica (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Thielaviopsis paradoxa (80 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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18 results found

Lot NumberCertificate TypeFechaArticulo
B2602466B2602466Certificate of AnalysisFeb 03, 2026 S401669
H2614062H2614062Certificate of AnalysisFeb 03, 2026 S401669
F2616021F2616021Certificate of AnalysisFeb 03, 2026 S401669
A2629467A2629467Certificate of AnalysisJan 30, 2026 S401669
A2629468A2629468Certificate of AnalysisJan 30, 2026 S401669
D2507687D2507687Certificate of AnalysisMar 24, 2025 S401669
D2507688D2507688Certificate of AnalysisMar 24, 2025 S401669
F2425232F2425232Certificate of AnalysisJun 11, 2024 S401669
F2425233F2425233Certificate of AnalysisJun 11, 2024 S401669
C2517686C2517686Certificate of AnalysisJun 11, 2024 S401669
A2621077A2621077Certificate of AnalysisDec 01, 2023 S401669
L2314233L2314233Certificate of AnalysisDec 01, 2023 S401669
L2314234L2314234Certificate of AnalysisDec 01, 2023 S401669
E2312260E2312260Certificate of AnalysisAug 08, 2022 S401669
G2325053G2325053Certificate of AnalysisAug 08, 2022 S401669
H2217707H2217707Certificate of AnalysisAug 08, 2022 S401669
H2217708H2217708Certificate of AnalysisAug 08, 2022 S401669
C2323018C2323018Certificate of AnalysisAug 08, 2022 S401669
Propiedades químicas y físicas
SolubilidadSoluble in water (50 mg/ml). Insoluble in ethanol.
SensibilidadMoisture Sensitive
Índice de refracción1.500
Punto de fusión (°C)270°C
Peso molecular84.007 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass83.9823 Da
Monoisotopic Mass83.9823 Da
Topological Polar Surface Area60.400 Ų
Heavy Atom Count5
Formal Charge0
Complexity33.900
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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Why Acridine Can Turn “Trace Molecules” into a Measurable Light Signal: A Mechanistic, Selection, and Troubleshooting Guide to Acridinium Ester Chemiluminescent Immunoassays (Including Product Tables 1–4)
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)
Amino Acid Oxidases: Oxygen-Dependent Oxidative Deamination Systems and Their Analytical and Applied Uses
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Chlorophyll: Structural Features, Physicochemical Properties, and Key Points for Research and Industrial Applications
Understanding Cbz (Benzyloxycarbonyl): Selection Logic and Practical Value of a Classical Amino Protecting Group
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
Technical Comparison and Method Selection for Hydroxyproline Determination
Coupling Mechanisms Between Terminal Reducing-Power Allocation in Photosynthetic Electron Transport and Metabolic Demand
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Experimental Judgment in Oxyma Coupling Systems: Coupling Efficiency, Racemization Control, and the HCN Risk in DIC-Based Systems
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Differences, Functions, and Selection Guidelines for Sodium Hydroxide Flakes, Granules, Liquid Caustic Soda, and Caustic Soda in Household and Personal Care Product Manufacturing: The Functional and Application Logic of Sodium Hydroxide
Why Daily Chemical Formulations Need Alkaline Ingredients: From pH Adjustment and Saponification to Detergency Boosting and Selection Logic
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Reactions and Applications of 3,3-Difluoroallyl Sulfonium Salts (DFASs): Small-Molecule gem-Difluoroallylation, Selective Peptide Modification, and Subsequent Functionalization
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
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Citations of This Product
Calculadoras de soluciones
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