N-Ethylmorpholine - for protein sequencing, ≥99.5%(GC) , CAS No.100-74-3

CAS: 100-74-3 Cat. No.: E104659 Fórmula: C₆H₁₃NO Peso molecular: 115.17 Beilstein Registry Number: 102969 Número EC: 202-885-0

GRADE & PURITY for Protein sequencing, ≥99.5%(GC)

Synonyms

Ethylmorpholine | CAS-100-74-3 | HSDB 1644 | Morpholine, 4-ethyl- | SCHEMBL3167 | CCRIS 4818 | E0145 | 4-27-00-00023 (Beilstein Handbook Reference) | 6LB | DTXCID205312 | NCGC00258655-01 | Dabco NEM | UNII-ECM0G991FQ | 4-Ethylmorpholine | 4-ethyl-morpholi

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice,FedEx DG Service

Specifications

Sinónimos

Ethylmorpholine | CAS-100-74-3 | HSDB 1644 | Morpholine, 4-ethyl- | SCHEMBL3167 | CCRIS 4818 | E0145 | 4-27-00-00023 (Beilstein Handbook Reference) | 6LB | DTXCID205312 | NCGC00258655-01 | Dabco NEM | UNII-ECM0G991FQ | 4-Ethylmorpholine | 4-ethyl-morpholi

Especificaciones y pureza

for protein sequencing, ≥99.5%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C,Argon charged

Enviado en

Wet ice,FedEx DG Service

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

Grado

para la secuenciación de proteínas

Pureza

≥99.5%(GC)

Nombres e identificadores

• Pubchem Sid: 504751380
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751380
• Sonrisas canónicas: CCN1CCOCC1
• IUPAC Name: 4-ethylmorpholine
• InChIKey: HVCNXQOWACZAFN-UHFFFAOYSA-N
• INCHI: 1S/C6H13NO/c1-2-7-3-5-8-6-4-7/h2-6H2,1H3
• Isómeros SMILES: CCN1CCOCC1
• WGK Alemania: 1
• RTECS: QE4025000
• Número ONU: 1993
• Grupo de embalaje: I
• Peso molecular: 115.17
• Beilstein: 102969
• Reaxy-Rn: 102969
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102969&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: Trialkylamines Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Morpholine - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - 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: 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

• Solubilidad: Miscible with water.
• Sensibilidad: Moisture sensitive.air sensitive， light sensitive ，heat sensitive
• Índice de refracción: 1.441
• Punto de inflamación (°C): (open cup)32℃
• Punto de ebullición (°C): 138°C
• Punto de fusión (°C): -63°C
• Peso molecular: 115.170 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 115.1 Da
• Monoisotopic Mass: 115.1 Da
• Topological Polar Surface Area: 12.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 59.500
• 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. Fan Liu, Wenbo Li, Junjie Yang, Dongxiao Ji, Yuan Liang, Hengtao Liang, Xiang Li, Pengju Han, Zupei Yuan, Jianxin He, Weili Shao.  (2023)  MOF-808 on Polyacrylonitrile Nanofibers for Degradation of Chemical Warfare Agents.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.3c03766]

2. Shiyi Chen, Feiyang Tian, Juan Peng, Yan Meng, Yu Wang, Xiaogang He, Qian Wang, Ganghui Chu.  (2023)  Turning Zr(IV) into a phosphate ester mimetic enzyme via de novo synthesis for hydrolyzing organophosphorus warfare agents and rapid activity prediction by near-infrared spectroscopy.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.109379]

3. Cai Chunqi, Chen Qingqing, Su Hongyan, Huang Pengcheng, Mao Junjie, Wu Fang-Ying.  (2023)  Single copper sites dispersed on metal-organic frameworks boost the degradation of nerve agent simulants.  Science China-Materials,  66  (6): (2475-2482).  [PMID:] [10.1007/s40843-022-2378-8]

4. Xuejiao Wang, Jing Yang, Ming Zhang, Qian Hu, Bai-Xue Li, Jin Qu, Zhong-Zhen Yu, Dongzhi Yang.  (2023)  Spontaneously super-hygroscopic MOF-gel microreactors for efficient detoxification of nerve agent simulant in atmospheric environments.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2023.122516]

5. Sun Yuhuan, Zhao Chuanqi, Cui Tingting, Qin Hongshuang, Niu Jingsheng, Ren Jinsong, Qu Xiaogang.  (2020)  Near-infrared-traceable DNA nano-hydrolase: specific eradication of telomeric G-overhang in vivo.  NUCLEIC ACIDS RESEARCH,  48  (17): (9986-9994).  [PMID:32853337] [10.1093/nar/gkaa693]

6. Linna Song, Tianyu Zhao, Dongzhi Yang, Xuejiao Wang, Xinmin Hao, Yaxin Liu, Shiyi Zhang, Zhong-Zhen Yu.  (2020)  Photothermal graphene/UiO-66-NH2 fabrics for ultrafast catalytic degradation of chemical warfare agent simulants.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:32120207] [10.1016/j.jhazmat.2020.122332]

7. Yuyang Liu, Shiyin Zhao, Yujiao Li, Jian Huang, Xuheng Yang, Jianfang Wang, Cheng-an Tao.  (2024)  Mechanically Enhanced Detoxification of Chemical Warfare Agent Simulants by a Two-Dimensional Piezoresponsive Metal–Organic Framework.  Nanomaterials,  14  (7): (559).  [PMID:38607094] [10.3390/nano14070559]

8. Mai Luo, Yao Peng, Jihai Cai, Tiantian Jiang, Sheng Gong, Shiyao Hua, Ting Wang, Sijia Wu, Shuangpeng Wang, Jinchao Wei, Peng Li.  (2025)  Bifunctional metal-organic framework Nanozymes with flexibly tunable valence states for dual-mode detection of organophosphorus pesticides.  FOOD CHEMISTRY,      [PMID:40749482] [10.1016/j.foodchem.2025.145711]

9. Wen-Xuan Jia, Ming-Ming Tao, Xin-Yu Wang, Yan-Feng Huang, Ying Li.  (2024)  Bimetallic MOFs-derived four-in-one CeCuOx/C nanozyme and its application for colorimetric detection of cysteine based on oxidase mimics.  Talanta Open,      [PMID:] [10.1016/j.talo.2024.100292]

10. Xuejiao Wang, Yu-Xuan Zheng, Chen Ding, Ming Zhang, Zhong-Zhen Yu, Shaobin Wang, Dongzhi Yang.  (2025)  Asymmetric Nanofiber Membranes for Simultaneous Moisture Adsorption and Rapid Catalytic Hydrolysis of Nerve Agent Simulants in Atmospheric Environments.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202504379]

11. Renqing Yang, Xiaowei Huang, Zeyan Liu, Zhihua Li, Xinai Zhang, Zhecong Yuan, Shujie Gao, Jiyong Shi, Xiaobo Zou.  (2025)  Highly efficient degradation of organophosphorus pesticides by bimetallic nanozyme with enhanced hydrogen-bonding interactions.  Journal of Water Process Engineering,      [PMID:] [10.1016/j.jwpe.2025.109251]