Guanidine Hydrobromide - ≥98%(T) , CAS No.19244-98-5

CAS: 19244-98-5 Cat. No.: G156807 Fórmula: CH₅N₃·HBr Peso molecular: 139.98 Número CE: 242-909-7

GRADE & PURITY ≥98%(T)

Synonyms

J-012443 | G0449 | MFCD03094062 | AS-59828 | Guanidinium Bromide | T72005 | GuanidineHydrobromide | Guanidine Monohydrobromide | AKOS037645293 | guanidine;hydrobromide | Guanidine bromide | guanidine hydrobromide | Guanidinium bromide, >=99%, anhydrous |

Storage

Room temperature,Argon charged

Shipped In

Normal

Visão geral

Organohalide based perovskites have emerged as an important class of material for solar cell applications. Our perovskites precursors with extremely low water contents are useful for synthesizing mixed cation or anion perovskites needed for the optimization of the band gap, carrier diffusion length and power conversion efficiency of perovskites based solar cells.

Specifications

Sinónimos

J-012443 | G0449 | MFCD03094062 | AS-59828 | Guanidinium Bromide | T72005 | GuanidineHydrobromide | Guanidine Monohydrobromide | AKOS037645293 | guanidine;hydrobromide | Guanidine bromide | guanidine hydrobromide | Guanidinium bromide, >=99%, anhydrous |

Especificações e pureza

≥98%(T)

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

Normal

Pureza

≥98%(T)

Nomes e identificadores

Pubchem Sid

508816273

Sorrisos canónicos

C(=N)(N)N.Br

IUPAC Name

guanidine;hydrobromide

InChIKey

VQNVZLDDLJBKNS-UHFFFAOYSA-N

INCHI

1S/CH5N3.BrH/c2-1(3)4;/h(H5,2,3,4);1H

SMILES isoméricas

C(=N)(N)N.Br

Peso molecular

139.98

Reaxy-Rn

3907837

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3907837&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Guanidines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Guanidines
• Intermediate Tree Nodes: Not available
• Direct Parent: Guanidines
• Alternative Parents: Carboximidamides Organopnictogen compounds Imines Hydrocarbon derivatives Hydrobromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Guanidine - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Hydrobromide - Imine - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as guanidines. These are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.
• External Descriptors: Not available

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

Propriedades químicas e físicas

• Solubilidade: Soluble in water
• Sensibilidade: Moisture sensitive
• Ponto de fusão (°C): 191 °C
• Peso molecular: 139.980 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 138.975 Da
• Monoisotopic Mass: 138.975 Da
• Topological Polar Surface Area: 75.900 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 26.300
• 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

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