N-Nitrosomorpholine - ≥99%(GC) , CAS No.59-89-2

CAS: 59-89-2 Cat. No.: N163026 Peso molecular: 116.12 Número EC: 627-564-6

GRADE & PURITY ≥99%(GC)

Synonyms

SCHEMBL1578515 | DTXCID001056 | 4-Nitrosomorpholine 1.0 mg/ml in Methanol | BRN 0112139 | STL301087 | 4-Nitrosomorpholine | 4-Nitroso-morpholine | EN300-7323775 | NMOR | N0466 | Q22138414 | CHEBI:76326 | T72681 | 3L25FO7FN7 | DTXSID4021056 | 1219805-76-1

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

SCHEMBL1578515 | DTXCID001056 | 4-Nitrosomorpholine 1.0 mg/ml in Methanol | BRN 0112139 | STL301087 | 4-Nitrosomorpholine | 4-Nitroso-morpholine | EN300-7323775 | NMOR | N0466 | Q22138414 | CHEBI:76326 | T72681 | 3L25FO7FN7 | DTXSID4021056 | 1219805-76-1

Especificaciones y pureza

≥99%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥99%(GC)

Nombres e identificadores

• Pubchem Sid: 488179995
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488179995
• Sonrisas canónicas: C1COCCN1N=O
• IUPAC Name: 4-nitrosomorpholine
• InChIKey: ZKXDGKXYMTYWTB-UHFFFAOYSA-N
• INCHI: 1S/C4H8N2O2/c7-5-6-1-3-8-4-2-6/h1-4H2
• Isómeros SMILES: C1COCCN1N=O
• WGK Alemania: 2
• Número ONU: 2810
• Grupo de embalaje: I
• Peso molecular: 116.12
• Reaxy-Rn: 112139
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=112139&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Oxazinanes
      • Subclass Morpholines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Oxazinanes
• Subclass: Morpholines
• Intermediate Tree Nodes: Not available
• Direct Parent: Morpholines
• Alternative Parents: Organic N-nitroso compounds Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Morpholine - Organic n-nitroso compound - Organic nitroso compound - Oxacycle - Azacycle - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
• External Descriptors: nitrosamine

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Solubility in water: Completely soluble; Soluble in Methanol
• Sensibilidad: Air Sensitive
• Punto de congelación (°C): 29 °C
• Punto de ebullición (°C): 225 °C
• Punto de fusión (°C): 29 °C
• Peso molecular: 116.120 g/mol
• XLogP3: -0.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 116.059 Da
• Monoisotopic Mass: 116.059 Da
• Topological Polar Surface Area: 41.900 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 80.100
• 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

Referencias

1. Zhiqin Ding, Mengdie Cai, Weimin Gan, Ping Yuan, Lijun Wei, Xianglei Cheng.  (2022)  Studies on a novel method for the determination of nitrosamines in food by HPLC-UV-FLD coupling with terbium-doped carbon dots.  FOOD CHEMISTRY,      [PMID:] [10.1016/j.foodchem.2022.134894]

2. He Ying, Ding Haotian, Xia Xingya, Qi Wenyi, Wang Huaisong, Liu Wenyuan, Zheng Feng.  (2021)  GFP-fused yeast cells as whole-cell biosensors for genotoxicity evaluation of nitrosamines.  APPLIED MICROBIOLOGY AND BIOTECHNOLOGY,  105  (13): (5607-5616).  [PMID:34228183] [10.1007/s00253-021-11426-4]