Potassium hydrogen carbonate - PharmPure™,ChP , CAS No.298-14-6

CAS: 298-14-6 Cat. No.: P708366 Summenformel: KHCO₃ Molekulargewicht: 100.12 Beilstein Registry Number: 4535309 EG-Nummer: 206-059-0

QUALITÄT & REINHEIT PharmPure™, ChP

Synonyms

Potassium bicarbonate

Storage

Room temperature

Shipped In

Normal

Spezifikationen

Synonyme

Potassium bicarbonate

Spezifikationen & Reinheit

PharmPure™,ChP

Storage

Room temperature

Verschickt in

Normal

Note

ChP, PharmPure™

Namen und Kennungen

Pubchem Sid

528774261

Kanonisches Lächeln

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

IUPAC Name

potassium;hydrogen carbonate

InChIKey

TYJJADVDDVDEDZ-UHFFFAOYSA-M

INCHI

1S/CH2O3.K/c2-1(3)4;/h(H2,2,3,4);/q;+1/p-1

Isomere SMILES

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

WGK Deutschland

1

Molekulargewicht

100.12

Beilstein

4535309

Reaxy-Rn

4535309

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4535309&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Organic carbonic acids and derivatives
• Subclass: Organic carbonic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic carbonic acids
• Alternative Parents: Carbonate salts Organic potassium 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 potassium salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: 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: potassium salt - organic 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

Zugehörige Ziele (nicht menschlich)

Eretmocerus eremicus (13 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cucurbita maxima x Cucurbita moschata (14 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Amblyseius swirskii (12 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Podosphaera xanthii (125 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Lagenaria siceraria (14 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: 362 g/L
• Empfindlichkeit: Moisture sensitive.
• Brechungsindex: 1.482
• Molekulargewicht: 100.115 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 99.9563 Da
• Monoisotopic Mass: 99.9563 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