Guanylurea Phosphate - ≥98%(T) , CAS No.36897-89-9

CAS: 36897-89-9 Cat. No.: G156819 Peso molecular: 200.09 Número EC: 253-264-6

GRADE & PURITY ≥98%(T)

Synonyms

NSC267685 | NSC-267685 | APINON 404 | guanyl urea phosphate | D0432 | Dicyandiamidine Phosphate | NSC7762 | NSC-7762 | ZHURYQINAXWNAH-UHFFFAOYSA-N | Q27259565 | Urea,N-(aminoiminomethyl)-,phosphate(1:x) | Guanylurea xPhosphate | Amidinourea phosphate | ca

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

NSC267685 | NSC-267685 | APINON 404 | guanyl urea phosphate | D0432 | Dicyandiamidine Phosphate | NSC7762 | NSC-7762 | ZHURYQINAXWNAH-UHFFFAOYSA-N | Q27259565 | Urea, N-(aminoiminomethyl)-, phosphate(1:x) | Guanylurea xPhosphate | Amidinourea phosphate | ca

Especificaciones y pureza

≥98%(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(T)

Nombres e identificadores

• Pubchem Sid: 488186407
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186407
• Sonrisas canónicas: C(=NC(=O)N)(N)N.OP(=O)(O)O
• IUPAC Name: diaminomethylideneurea;phosphoric acid
• InChIKey: ZHURYQINAXWNAH-UHFFFAOYSA-N
• INCHI: 1S/C2H6N4O.H3O4P/c3-1(4)6-2(5)7;1-5(2,3)4/h(H6,3,4,5,6,7);(H3,1,2,3,4)
• Isómeros SMILES: C(=NC(=O)N)(N)N.OP(=O)(O)O
• CAS alternativo: 17675-60-4
• Peso molecular: 200.09
• Reaxy-Rn: 7180036
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7180036&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic phosphoric acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic phosphoric acids and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic phosphoric acids and derivatives
• Alternative Parents: Organic carbonic acids and derivatives Guanidines Propargyl-type 1,3-dipolar organic compounds Carboximidamides Organopnictogen compounds Organic oxides Imines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic phosphoric acid derivative - Guanidine - Carbonic acid derivative - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Imine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organic phosphoric acids and derivatives. These are organic compounds containing phosphoric acid or a derivative thereof.
• 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

Propiedades químicas y físicas

• Punto de fusión (°C): 184 °C
• Peso molecular: 200.090 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 200.031 Da
• Monoisotopic Mass: 200.031 Da
• Topological Polar Surface Area: 185.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 152.000
• 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