2-[2-(2-Chloroethoxy)ethoxy]ethanol - ≥96%(GC) , CAS No.5197-62-6

CAS: 5197-62-6 Cat. No.: C133890 Summenformel: C₆H₁₃ClO₃ Molekulargewicht: 168.62 Beilstein Registry Number: 1(3)2105 EG-Nummer: 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

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyme

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

Spezifikationen & Reinheit

≥96%(GC)

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Hinweis

Refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Reinheit

≥96%(GC)

Namen und Kennungen

• Pubchem Sid: 488185635
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185635
• Kanonisches Lächeln: 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
• Isomere SMILES: C(COCCOCCCl)O
• WGK Deutschland: 3
• Molekulargewicht: 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
    • Klasse Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Air sensitive;Heat sensitive
• Brechungsindex: 1.4560 to 1.4590
• Flammpunkt (°F): 224.6 °F
• Flammpunkt (°C): 107°C
• Siedepunkt (°C): 232°C
• Molekulargewicht: 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

Referenzen

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]