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

CAS: 19244-98-5 Cat. No.: G156807 Formule: CH₅N₃·HBr Poids moléculaire: 139.98 Numéro CE: 242-909-7

QUALITÉ & PURETÉ ≥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

Vue d’ensemble

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.

Spécifications

Synonymes

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

Spécifications et pureté

≥98%(T)

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Pureté

≥98%(T)

Noms et identifiants

Pubchem Sid

508816273

Sourires canoniques

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

Isomères SMILES

C(=N)(N)N.Br

Poids moléculaire

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
• Description: 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

Propriétés chimiques et physiques

• Solubilité: Soluble in water
• Sensibilité: Moisture sensitive
• Point de fusion (°C): 191 °C
• Poids moléculaire: 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

XLogP3