2-[2-(2-cloroetossi)etossido]etanolo - ≥96%(GC) , CAS No.5197-62-6

CAS: 5197-62-6 Cat. No.: C133890 Formula: C₆H₁₃ClO₃ Peso molecolare: 168.62 Beilstein Registry Number: 1(3)2105 Numero EC: 225-984-0

GRADE & PURITY ≥96%(GC)

Synonyms

NSC2636 | EN300-134537 | AKOS006220767 | NSC 2636 | EINECS 225-984-0 | Ethanol, 2-(2-(2-chloroethoxy)ethoxy)- | MPA47W5DV5 | DTXSID30199936 | SCHEMBL315062 | Triethylene glycol monochlorohydrin | 2-[2-(2-Chloroethoxy)ethoxy]ethanol, 96% | MFCD02258625 | C

Storage

Conservare a 2-8°C, con carica di argon

Shipped In

Ghiaccio umido

Specifications

Sinonimi

NSC2636 | EN300-134537 | AKOS006220767 | NSC 2636 | EINECS 225-984-0 | Ethanol, 2-(2-(2-chloroethoxy)ethoxy)- | MPA47W5DV5 | DTXSID30199936 | SCHEMBL315062 | Triethylene glycol monochlorohydrin | 2-[2-(2-Chloroethoxy)ethoxy]ethanol, 96% | MFCD02258625 | C

Specifiche e purezza

≥96%(GC)

Condizioni di conservazione di stoccaggio

Conservare a 2-8°C, con carica di argon

Spedito in

Ghiaccio umido

Nota

Per ulteriori informazioni, consultare la SDS. Avete bisogno di ulteriori consigli su solubilità, uso e manipolazione? Visitate la pagina delle domande frequenti (FAQ) per maggiori dettagli.

Purezza

≥96%(GC)

Nomi e identificatori

• Pubchem Sid: 488185635
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185635
• Sorrisi canonici: C(COCCOCCCl)O
• IUPAC Name: 2-[2-(2-chloroethoxy)ethoxy]ethanol
• InChIKey: KECMLGZOQMJIBM-UHFFFAOYSA-N
• INCHI: 1S/C6H13ClO3/c7-1-3-9-5-6-10-4-2-8/h8H,1-6H2
• Isomeri SMILES: C(COCCOCCCl)O
• WGK Germania: 3
• Peso molecolare: 168.62
• Beilstein: 1(3)2105
• Reaxy-Rn: 1739194
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1739194&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Primary alcohols Organochlorides Hydrocarbon derivatives Alkyl chlorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Primary alcohol - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• 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

Proprietà chimiche e fisiche

• Sensibilità: Air sensitive;Heat sensitive
• Indice di rifrazione: 1.4560 to 1.4590
• Punto di infiammabilità (°F): 224.6 °F
• Punto di infiammabilità (°C): 107°C
• Punto di ebollizione (°C): 232°C
• Peso molecolare: 168.620 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 168.055 Da
• Monoisotopic Mass: 168.055 Da
• Topological Polar Surface Area: 38.700 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 61.000
• 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

Riferimenti

1. Guanyu Chi, Yinghua Lv, Shuang Chao, Chenxi Hou, Yuxin Pei, Zhichao Pei.  (2022)  Glyconanoparticles with Activatable Near-Infrared Probes for Tumor-Cell Imaging and Targeted Drug Delivery.  International Journal of Nanomedicine,      [PMID:35401000] [10.2147/IJN.S337082]

2. Lingling Peng, Mingzhen Shi, Yi Pan, Zhuoheng Tu, Xingbang Hu, Xiaomin Zhang, Youting Wu.  (2022)  Ultrahigh carbon monoxide capture by novel protic cuprous-functionalized dicationic ionic liquids through complexation interactions.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.138519]

3. Chen Shao, Kun Shang, Huaibao Xu, Yu Zhang, Zhichao Pei, Yuxin Pei.  (2018)  Facile fabrication of hypericin-entrapped glyconanoparticles for targeted photodynamic therapy.  International Journal of Nanomedicine,      [PMID:30087563] [10.2147/IJN.S161262]

4. Huizhe Niu, Ying Lu, Zhe Zhang, Manni Li, Jiaxiang Liu, Fan Qu, Zemin He, Wenqi Song, Yuzhen Zhao, Xiaoqin Liu, Zongcheng Miao.  (2025)  Plicated mesoporous silica nanoparticles integrated poly(ionic liquids) composite polymer electrolyte for solid‐state lithium-ion batteries.  ENERGY,      [PMID:] [10.1016/j.energy.2025.135901]

5. Zhanyu Li, Yiman Gu, Yanchao Zhang, Zhe Wang, Di Liu, Tianming Dong, Xiaoyu Chi, Jingyi Wu, Yijia Lei.  (2024)  Poly (biphenyl-isatin-piperidine) anion exchange membrane with high hydroxide conductivity based on hydrophilic alkoxy spacer chains.  Materials Today Chemistry,      [PMID:] [10.1016/j.mtchem.2024.102122]

6. Rihui Liang, Maoxin Zhang, Bo Yuan, Wei Feng.  (2025)  Regulation of Molecular Solar Thermal Energy Storage Capacity of Azobenzene and Acrylic Ester Copolymers through Hydrogen Bonding and Application in Solar Thermal Cells.  ACS Applied Materials & Interfaces,      [PMID:40662601] [10.1021/acsami.5c05615]