Calcium carbonate - AR, ≥99% , CAS No.471-34-1

CAS: 471-34-1 Cat. No.: C111980 Formula: CaCO₃ Peso molecolare: 100.09 Beilstein Registry Number: 8008338 Numero EC: 207-439-9

GRADE & PURITY AR, ≥99%

Synonyms

Garolite SA | BS 32 | Camel-wite | Calcium carbonate (USP) | Chemcarb | INS NO.170(I) | Levigated chalk | Albacar | Calcicoll | Calofort S | carbonato de calcio | EPA Pesticide Chemical Code 073502 | Caltec | CI 77220 | Kotamite | Microcarb | Multiflex SC

Storage

Room temperature

Shipped In

Normal

Panoramica

Iron-Catalyzed Efficient Synthesis of Amides from Aldehydes and Amine Hydrochloride Salts
Calcium carbonate may be used:
As a pore generating agent to prepare porous ceramics.
As chelometric standard for the standardization of EDTA solution.
To extract aluminium by microwave induced thermal activation of coal fly ash (CFA). 

Specifications

Sinonimi

Garolite SA | BS 32 | Camel-wite | Calcium carbonate (USP) | Chemcarb | INS NO.170(I) | Levigated chalk | Albacar | Calcicoll | Calofort S | carbonato de calcio | EPA Pesticide Chemical Code 073502 | Caltec | CI 77220 | Kotamite | Microcarb | Multiflex SC

Specifiche e purezza

AR, ≥99%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Grado

AR

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

488181081

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488181081

Sorrisi canonici

C(=O)([O-])[O-].[Ca+2]

IUPAC Name

calcium;carbonate

InChIKey

VTYYLEPIZMXCLO-UHFFFAOYSA-L

INCHI

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

Isomeri SMILES

C(=O)([O-])[O-].[Ca+2]

RTECS

FF9335000

Peso molecolare

100.09

Beilstein

8008338

Reaxy-Rn

8008338

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8008338&ln=

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 calcium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carbonate salt - Carbonic acid - Organic calcium salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - 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: calcium salt - one-carbon compound - carbonate 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive.
• Punto di fusione (°C): 800°C
• Peso molecolare: 100.090 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 99.9473 Da
• Monoisotopic Mass: 99.9473 Da
• Topological Polar Surface Area: 63.200 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 18.800
• 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