Sodium bicarbonate - anhydrous, ACS, ≥99.7% , CAS No.144-55-8

CAS: 144-55-8 Cat. No.: S432108 Summenformel: NaHCO3 Molekulargewicht: 84.01 Beilstein Registry Number: 4153970 EG-Nummer: 205-633-8
Zu bestellen verfügbar
GRADE & PURITY Anhydrous Grade ? Anhydrous grade — water removed and packaged dry for moisture-sensitive chemistry. Use in reactions where even trace water would interfere or quench. ACS ? ACS grade — meets American Chemical Society specifications, the analytical benchmark in the US. Use for analytical and QC work needing ACS-defined purity. ≥99.7%
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
Room temperature
★
Size
Deutschland (EU)
USA*
Price
Qty
500g
S432108-500g
—
1 Auf Lager
51,98€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

anhydrous, ACS, ≥99.7% ACS,Anhydrous Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1635 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyme
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
Spezifikationen & Reinheit
anhydrous, ACS, ≥99.7%
Storage
Room temperature
Note
ACS, Anhydrous Grade
Reinheit
≥99.7%
Namen und Kennungen
Pubchem Sid528774259
Kanonisches LächelnC(=O)(O)[O-].[Na+]
IUPAC Namesodium;hydrogen carbonate
InChIKeyUIIMBOGNXHQVGW-UHFFFAOYSA-M
INCHI1S/CH2O3.Na/c2-1(3)4;/h(H2,2,3,4);/q;+1/p-1
Isomere SMILES C(=O)(O)[O-].[Na+]
RTECS VZ0950000
Alternative CAS-Nummer 144-55-8,7542-12-3 (unspecified hydrochloride salt)
MeSH-Eintrag Baking Soda;Bicarbonate, Sodium;Carbonic Acid Monosodium Salt;Hydrogen Carbonate, Sodium;Soda, Baking;Sodium Bicarbonate;Sodium Hydrogen Carbonate
Molekulargewicht 84.01
Beilstein 4153970

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
KlasseOrganic 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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
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
Zugehörige Ziele (nicht menschlich)
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
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

18 results found

Lot NumberCertificate TypeDatumArtikel
H2514428Certificate of AnalysisAug 18, 2025 S432108
H2514427Certificate of AnalysisAug 18, 2025 S432108
H2514399Certificate of AnalysisAug 18, 2025 S432108
H2514398Certificate of AnalysisAug 18, 2025 S432108
E2612119Certificate of AnalysisAug 18, 2025 S432108
D2501533Certificate of AnalysisApr 14, 2025 S432108
D2501532Certificate of AnalysisApr 11, 2025 S432108
E2521020Certificate of AnalysisApr 11, 2025 S432108
D2501535Certificate of AnalysisApr 11, 2025 S432108
D2501534Certificate of AnalysisApr 11, 2025 S432108
K2406151Certificate of AnalysisNov 08, 2024 S432108
E2327116Certificate of AnalysisMay 09, 2023 S432108
E2327114Certificate of AnalysisMay 09, 2023 S432108
E2327109Certificate of AnalysisMay 09, 2023 S432108
G2423046Certificate of AnalysisMay 09, 2023 S432108
E23261179Certificate of AnalysisMay 09, 2023 S432108
C2413073Certificate of AnalysisMay 09, 2023 S432108
L2313066Certificate of AnalysisMay 09, 2023 S432108
Chemische und physikalische Eigenschaften
Brechungsindex1.500
Schmelzpunkt (°C)270°C
Molekulargewicht84.007 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 und Artikel
Aladdin@Guidelines for the formulation of commonly used buffers for biological experiments
The Guide to Anhydrous Grade for Reagents
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
Lösungsrechner
Bewertungen

Kundenbewertungen

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.