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

CAS: 144-55-8 Cat. No.: S112337 Formula: NaHCO₃ Peso molecolare: 84.01 Beilstein Registry Number: 4153970 Numero EC: 205-633-8

QUALITÀ & PUREZZA HPLC grade, ≥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

Panoramica

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.

Specifiche

Sinonimi

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

Specifiche e purezza

HPLC grade, ≥99.8%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

Normal

Grado

HPLC grade

Purezza

≥99.8%

Nomi e identificatori

Sorrisi canonici

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

Isomeri SMILES

C(=O)(O)[O-].[Na+]

RTECS

VZ0950000

CAS alternativo

144-55-8,7542-12-3 (unspecified hydrochloride salt)

Termini MeSH

Baking Soda;Bicarbonate, Sodium;Carbonic Acid Monosodium Salt;Hydrogen Carbonate, Sodium;Soda, Baking;Sodium Bicarbonate;Sodium Hydrogen Carbonate

Peso molecolare

84.01

Beilstein

4153970

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Organic carbonic acids and derivatives
      • Subclass Organic carbonic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Organic carbonic acids and derivatives
• Subclass: Organic carbonic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic carbonic acids
• Alternative Parents: Carbonate salts Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic 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
• Descrizione: This 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water (50 mg/ml). Insoluble in ethanol.
• Sensibilità: Moisture Sensitive
• Indice di rifrazione: 1.500
• Punto di fusione (°C): 270°C
• Peso molecolare: 84.007 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 83.9823 Da
• Monoisotopic Mass: 83.9823 Da
• Topological Polar Surface Area: 60.400 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 33.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3