Sodium bicarbonate - HPLC grade, ≥99.8% , CAS No.144-55-8

CAS: 144-55-8 Cat. No.: S112337 Fórmula: NaHCO3 Peso molecular: 84.01 Beilstein Registry Number: 4153970 Número CE: 205-633-8
Disponível para encomenda
GRAU & PUREZA HPLC grade ? HPLC grade — purity and low UV-absorbing impurities suited to liquid chromatography. Use as the everyday solvent/reagent for routine HPLC. ≥99.8%
Synonyms
Baking soda | Natrii hydrogencarbonas | Natrum bicarbonicum | Sodium hydrogen carbonate | Natrii hydrogenocarbonas | Natrium bicarbonicum | AssuredBug Bite Relief | Monosodium hydrogen carbonate | Sel De vichy | CHEBI:32139 | natriumhydrogencarbonat
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Tamanho
USA
Alemanha (EU)*
Preço
Qtd
500g
S112337-500g
3 Em stock
—

65,90US$

80,90US$
Gravar 15,00 US$ (18.54%)
Enter a quantity for the sizes you want to add.
🧪
Por que este grau

HPLC grade, ≥99.8% HPLC grade para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

🌡

Armazenamento e envio

Room temperature,Argon charged Envio Normal. Consulte o COA específico do lote para obter as especificações exatas.

📋

Documentos de qualidade

SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

📚

Comprovação documental

Citado em 1650 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

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.

Especificações

Sinónimos
Baking soda | Natrii hydrogencarbonas | Natrum bicarbonicum | Sodium hydrogen carbonate | Natrii hydrogenocarbonas | Natrium bicarbonicum | AssuredBug Bite Relief | Monosodium hydrogen carbonate | Sel De vichy | CHEBI:32139 | natriumhydrogencarbonat
Especificações e pureza
HPLC grade, ≥99.8%
Condições de armazenamento de armazenamento
Room temperature,Argon charged
Enviado em
Normal
Grau
HPLC grade
Pureza
≥99.8%
Nomes e identificadores
Sorrisos canónicos
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
SMILES isoméricas
C(=O)(O)[O-].[Na+]
RTECS
VZ0950000
CAS alternativo
144-55-8,7542-12-3 (unspecified hydrochloride salt)
Termos 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

Documentação

📋 Ficha de dados de segurança (FDS)

Documento abrangente sobre perigos, manuseamento, armazenamento e conformidade regulamentar.

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

✅ Certificado de análise (COA)

Dados de qualidade específicos do lote. Introduza o número de lote para obter o COA exato.

Consultar COA →

📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

Ver ficha técnica →

🔬 Folha de especificações

Atributos de qualidade completos e critérios de aceitação para este grau.

Ver folha de especificações →

Dados avançados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseOrganic 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
DescriçãoThis 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
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (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
Alvos associados (não 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)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusarium verticillioides (912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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 ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

12 results found

Lot NumberCertificate TypeDataItem
G2222810G2222810Certificate of AnalysisMay 09, 2026 S112337
C2617309C2617309Certificate of AnalysisMar 09, 2026 S112337
C2618469C2618469Certificate of AnalysisMar 09, 2026 S112337
C2618475C2618475Certificate of AnalysisMar 09, 2026 S112337
E2521591E2521591Certificate of AnalysisMay 12, 2025 S112337
E2521603E2521603Certificate of AnalysisMay 12, 2025 S112337
J2430603J2430603Certificate of AnalysisOct 18, 2024 S112337
G2222807G2222807Certificate of AnalysisJul 11, 2022 S112337
C2203120C2203120Certificate of AnalysisFeb 16, 2022 S112337
C2203289C2203289Certificate of AnalysisFeb 16, 2022 S112337
B2207507B2207507Certificate of AnalysisJan 19, 2022 S112337
D2113131D2113131Certificate of AnalysisApr 22, 2021 S112337
Propriedades químicas e físicas
SolubilidadeSoluble in water (50 mg/ml). Insoluble in ethanol.
SensibilidadeMoisture Sensitive
Índice de refração1.500
Ponto de fusão (°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
FAQs e artigos
Fura-2 AM Staining Protocol
Introduction: “Suitable for HPLC” (HPLC Grade)
FAQs on Animal Cell Culture Media
Frequently Asked Questions about Cell Culture
Operational Guide for Fluorescent Labeling of Antibodies Using AF594 NHS Ester
FAQ on Cell Culture Serum
General Principles of Antibody Labeling with NHS-Activated Esters, F/P Calculation, and Troubleshooting Guide
TEMPO-Catalyzed Oxidation Quick Reference (Alcohol Oxidation Focus): Three Regeneration Routes (NaOCl / Cu–O₂ / PIDA) + Selection & Troubleshooting
Physicochemical Properties, Staining Mechanisms, and Practical Application Specifications of Hematoxylin
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 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
Phytase: Enzymological Properties, Mechanism of Action, and Applications in Feed and Food
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
Injectable Thermosensitive Gels: Gelation Behavior, Rheological Properties, and Drug Release Characteristics
Experimental Assessment of Fmoc Introduction Routes: Impurity Profile Differences, Raw Material Carryover, and Quality Control
From Functional Groups to Experimental Decision-Making: Protein Crosslinker Selection and Experimental Essentials
PVAc, VAE, and Vinyl Acetate-Based Emulsions: Film-Forming Logic and Performance Boundaries in Architectural Coatings
Application of Shellac, a Natural Film-Forming Resin, in Coatings: Alcohol-Soluble Fast-Drying Film Formation, Sealing and Repair, and Performance Boundaries
Why LABSA (Sulfonic Acid) Is Commonly Used in Household Cleaning Formulations: Neutralization Mechanism, Detergency Action, and Formulation Application Points
Differences, Mechanisms of Action, and Selection of Sodium Metasilicate and Sodium Tripolyphosphate in Detergent and Cleaning Formulations
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
Why Limonene Can Soften Greasy Soils Yet Is Difficult to Dissolve in Water: Understanding the Cleaning Mechanism and Formulation Applications of Naturally Derived Solvents from Molecular Structure
How Can Sodium Tripolyphosphate (STPP) Be Replaced? From Detergency Mechanisms to Formulation Choices for Low-Phosphorus/Phosphorus-Free Builder Systems
More Than a pH Adjuster: Mechanisms, Selection Logic, and Alternative Acid Source Analysis of Citric Acid in Home-Care Cleaning
Sodium Metasilicate in Cleaning Applications: Hydration-Form Differences, Mechanisms of Action, and Selection Logic
Differences and Application Selection of Cassava- and Corn-Based Pregelatinized Starch in Neutral Putty Formulations
Skin Mechanism of Action of Pro-Xylane: From C-Xyloside Priming and CS/DS Chain Remodeling to the Dermal–Epidermal Junction
How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example
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
Citations of This Product
Calculadoras de soluções
Revisões

Avaliações dos Clientes

Deseja que lhe enviemos uma mensagem quando tivermos descontos disponíveis?

Lembrar-me mais tarde

Obrigado! Por favor, verifique a sua caixa de entrada de e-mail para confirmar.

Ops! As notificações estão desativadas.