Urea - for electrophoresis, ≥99.5%(T) , CAS No.57-13-6

CAS: 57-13-6 Cat. No.: U111901 Formula: H₂NCONH₂ Peso molecolare: 60.06 Beilstein Registry Number: 635724 Numero EC: 200-315-5 PubChem CID: 1176

QUALITÀ & PUREZZA Suitable for electrophoresis, ≥99.5%(T)

Synonyms

Carbonyldiamide | Onychomal | Ultra Mide | UNII-8W8T17847W | UREA [EP MONOGRAPH] | UREA COMPONENT OF CALMURID HC | Ureacin-10 lotion | EINECS 200-315-5 | Urevert | CALMURID HC COMPONENT UREA | Carbamide;Carbonyldiamide | Carbonyldiamine | Panafil | Urea (

Storage

Room temperature

Shipped In

Normal

Specifiche

Sinonimi

Carbonyldiamide | Onychomal | Ultra Mide | UNII-8W8T17847W | UREA [EP MONOGRAPH] | UREA COMPONENT OF CALMURID HC | Ureacin-10 lotion | EINECS 200-315-5 | Urevert | CALMURID HC COMPONENT UREA | Carbamide;Carbonyldiamide | Carbonyldiamine | Panafil | Urea (

Specifiche e purezza

for electrophoresis, ≥99.5%(T)

Meccanismi biochimici e fisiologici

Urea participates in the metabolism of nitrogen-containing substances. When used as fertilizer, it can serve as a nitrogen source. Urea is used to manufacture compounds. It is widely used as fertilizer and animal feed additive in the agricultural field, a

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Grado

Adatto all'elettroforesi

Purezza

≥99.5%(T)

Nomi e identificatori

Pubchem Sid

508813338

Sorrisi canonici

C(=O)(N)N

IUPAC Name

urea

InChIKey

XSQUKJJJFZCRTK-UHFFFAOYSA-N

INCHI

1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)

Isomeri SMILES

C(=O)(N)N

WGK Germania

1

RTECS

YR6250000

PubChem CID

1176

Peso molecolare

60.06

Beilstein

635724

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Organic carbonic acids and derivatives
      • Subclass Ureas

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Organic carbonic acids and derivatives
• Subclass: Ureas
• Intermediate Tree Nodes: Not available
• Direct Parent: Ureas
• Alternative Parents: Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Urea - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as ureas. These are compounds containing two amine groups joined by a carbonyl (C=O) functional group.
• External Descriptors: a small molecule

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

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water, methanol, ethanol, slightly soluble in ether, chloroform, and benzene.
• Sensibilità: Moisture sensitive.
• Punto di fusione (°C): 132-135 °C (lit.)
• Peso molecolare: 60.056 g/mol
• XLogP3: -1.400
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 60.0324 Da
• Monoisotopic Mass: 60.0324 Da
• Topological Polar Surface Area: 69.100 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 29.000
• 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: 1