Aminoguanidine hemisulfate salt - ≥98% , CAS No.996-19-0

CAS: 996-19-0 Cat. No.: A111133 Peso molecular: 123.12 Número EC: 213-628-7

GRADE & PURITY ≥98%

Synonyms

Tox21_111552_1 | DTXSID0046016 | pimagedine hemisulfate | Di(carbazamidine) sulphate | Aminoguanidine hemisulfate | R13YB310MU | Hydrazinecarboximidamide hemisulfate | aminoguanidinesulfate | CCG-204146 | NCGC00015082-09 | HMS3260I21 | W-100028 | Hydrazin

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

Tox21_111552_1 | DTXSID0046016 | pimagedine hemisulfate | Di(carbazamidine) sulphate | Aminoguanidine hemisulfate | R13YB310MU | Hydrazinecarboximidamide hemisulfate | aminoguanidinesulfate | CCG-204146 | NCGC00015082-09 | HMS3260I21 | W-100028 | Hydrazin

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488192691
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488192691
• Sonrisas canónicas: C(=NN)(N)N.C(=NN)(N)N.OS(=O)(=O)O
• IUPAC Name: 2-aminoguanidine;sulfuric acid
• InChIKey: VKGQPUZNCZPZKI-UHFFFAOYSA-N
• INCHI: 1S/2CH6N4.H2O4S/c2*2-1(3)5-4;1-5(2,3)4/h2*4H2,(H4,2,3,5);(H2,1,2,3,4)
• Isómeros SMILES: C(=NN)(N)N.C(=NN)(N)N.OS(=O)(=O)O
• WGK Alemania: 2
• Peso molecular: 123.12
• Reaxy-Rn: 18538574
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18538574&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic sulfuric acids and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic sulfuric acids and derivatives
• Alternative Parents: Guanidines Hydrazones Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Organic sulfuric acid or derivatives - Guanidine - Hydrazone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organic sulfuric acids and derivatives. These are organic compounds containing the sulfuric 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

Objetivos asociados (humanos)

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water
• Punto de fusión (°C): 200°C
• Peso molecular: 246.250 g/mol
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 0
• Exact Mass: 246.086 Da
• Monoisotopic Mass: 246.086 Da
• Topological Polar Surface Area: 264.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 123.000
• 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: 3

XLogP3

Referencias

1. Li Fu, Zerui Liu, Pengjie Dong, Yingshu Guo.  (2023)  Electrochemiluminescence Mechanistic Insights of CuInS2/ZnS Nanocrystals with Hydrazine Compounds as Co-reactants.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.3c06277]

2. Lei Wang, Wan-Yang Xu, Yi-Wen Tang, Feng Hu.  (2022)  Nitrative inactivation of thioredoxin-1 loses its protective effect in bleomycin-induced pulmonary fibrosis.  INTERNATIONAL IMMUNOPHARMACOLOGY,      [PMID:36087509] [10.1016/j.intimp.2022.109208]