1,4-Bis(2-hydroxyethoxy)benzene - ≥95%(GC) , CAS No.104-38-1

CAS: 104-38-1 Cat. No.: B151930 Peso molecular: 198.22 Beilstein Registry Number: 6(3)4406 Número EC: 203-197-3

GRADE & PURITY ≥95%(GC)

Synonyms

hydroquinone dihydroxyethyl ether | NSC1862 | NSC-1862 | 2,2'-p-Phenylenedioxydiethanol | BS-14346 | EINECS 203-197-3 | Ethanol,2'-(p-phenylenedioxy)di- | 2,2'-(Phenylenedioxy)diethanol | 2,2'-(p-Phenylenedioxy)diethanol | 1,4-Bis(beta-hydroxyethoxy)benze

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Product Application：

Hydroquinone bis(2-hydroxyethyl) ether is used to produce 1,4-bis-(2-bromo-ethoxy)-benzene.

Specifications

Sinónimos

hydroquinone dihydroxyethyl ether | NSC1862 | NSC-1862 | 2, 2'-p-Phenylenedioxydiethanol | BS-14346 | EINECS 203-197-3 | Ethanol, 2'-(p-phenylenedioxy)di- | 2, 2'-(Phenylenedioxy)diethanol | 2, 2'-(p-Phenylenedioxy)diethanol | 1, 4-Bis(beta-hydroxyethoxy)benze

Especificaciones y pureza

≥95%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥95%(GC)

Nombres e identificadores

• Pubchem Sid: 488183878
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183878
• Sonrisas canónicas: C1=CC(=CC=C1OCCO)OCCO
• IUPAC Name: 2-[4-(2-hydroxyethoxy)phenoxy]ethanol
• InChIKey: WTPYFJNYAMXZJG-UHFFFAOYSA-N
• INCHI: 1S/C10H14O4/c11-5-7-13-9-1-2-10(4-3-9)14-8-6-12/h1-4,11-12H,5-8H2
• Isómeros SMILES: C1=CC(=CC=C1OCCO)OCCO
• Peso molecular: 198.22
• Beilstein: 6(3)4406
• Reaxy-Rn: 514873
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=514873&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Phenol ethers

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Phenol ethers
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenol ethers
• Alternative Parents: Phenoxy compounds Alkyl aryl ethers Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.
• 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

Objetivos asociados (no humanos)

Pseudomonas aeruginosa (123386 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water
• Sensibilidad: Hygroscopic
• Punto de fusión (°C): 105 °C
• Peso molecular: 198.220 g/mol
• XLogP3: 0.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 198.089 Da
• Monoisotopic Mass: 198.089 Da
• Topological Polar Surface Area: 58.900 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 116.000
• 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

Referencias

1. Pandi Chen, Fenglong Li, Guyue Wang, Binbin Ying, Chao Chen, Ying Tian, Maosong Chen, Kyung Jin Lee, Wu Bin Ying, Jin Zhu.  (2023)  Toward Highly Matching the Dura Mater: A Polyurethane Integrating Biocompatible, Leak-Proof, and Self-Healing Properties.  MACROMOLECULAR BIOSCIENCE,      [PMID:37222304] [10.1002/mabi.202300111]

2. Huan Wang, Zhengzai Cheng, Lesly Dasilva Wandji Djouonkep, Linfeng Wang, Shuanpu Cai, Mario Gauthier.  (2023)  Synthesis and properties of biodegradable aliphatic–aromatic polyesters derived from 4-hydroxybenzaldehyde.  JOURNAL OF APPLIED POLYMER SCIENCE,  140  (29): (e54063).  [PMID:] [10.1002/app.54063]

3. Tao Xiong, Yi-Fu Zhang.  (2022)  Synthesis and properties of polyurethane acrylate oligomer based on polycaprolactone diol.  E-POLYMERS,  22  (1): (147-155).  [PMID:] [10.1515/epoly-2022-0009]

4. Fenglong Li, Zifa Xu, Han Hu, Zhengyang Kong, Chao Chen, Ying Tian, Wenwu Zhang, Wu Bin Ying, Ruoyu Zhang, Jin Zhu.  (2021)  A polyurethane integrating self-healing, anti-aging and controlled degradation for durable and eco-friendly E-skin.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2020.128363]

5. Wu Bin Ying, Haixiong Liu, Peiyuan Gao, Zhengyang Kong, Han Hu, Kai Wang, Ang Shen, Zhijin Jin, Lin Zheng, Hongxia Guo, Ruoyu Zhang, Jin Zhu.  (2020)  An anti-stress relaxation, anti-fatigue, mildew proof and self-healing poly(thiourethane-urethane) for durably stretchable electronics.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2020.127691]

6. Z. Yu, W.B. Ying, D. Pravarthana, Y.Y. Li, G.Y. Mao, Y.W. Liu, C. Hu, W.X. Zhang, P.X. He, Z.C. Zhong, S.X. Qu, R.Y. Zhang, J. Shang, J. Zhu, R.-W. Li.  (2020)  Stretchable tactile sensor with high sensitivity and dynamic stability based on vertically aligned urchin-shaped nanoparticles.  Materials Today Physics,      [PMID:] [10.1016/j.mtphys.2020.100219]

7. Guo Wei, Hang Xu, Li Chen, Zhiquan Li, Ren Liu.  (2018)  Isosorbide-based high performance UV-curable reactive diluents.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2018.10.028]

8. Jie Hu, Hengju Zhou, Xinyao Wang, Shiqiang Cui, Shouzhi Pu.  (2024)  Preparation of photochromic microcapsules with a diarylethene and polyurethane/chitosan for smart textiles.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2024.112546]

9. Li Shuo, Xu Tongan, Deng Ming, Jia Ruyan, Djouonkep Lesly Dasilva Wandji.  (2025)  Structure–Property Relationships of Renewable Ternary Polyesters Derived from Vanillin-Based Methyl Ester, Aliphatic Diacids, and Phenol Ether-Based Diols.  JOURNAL OF POLYMERS AND THE ENVIRONMENT,      [PMID:] [10.1007/s10924-025-03643-z]

10. Li-Wei Su, Ming-Hao Liu, Yang Jing, Peng-Yu Huang, Bo Jiang, Rui-Guang Xing, Xin Ge, Ya-Hui Li, Jin-Xiao Bao, Gao-Fei Pan.  (2025)  Recyclable flame retardant, luminescent, and transparent thermoplastic polyurethanes: applications in light conversion films for flexible solar cells.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.164436]

11. Li-Wei Su, Tian-Yu Su, Zheng Zhao, Ming-Hao Liu, Rui-Guang Xing, Xin Ge, Li-Na Jia, Ya-Hui Li, Jin-Xiao Bao, Gao-Fei Pan.  (2025)  High-Strength, Flame-Retardant, UV-Resistant Polyurethane Elastomers Realized by Synergizing Nitrogen-Phosphorus-Containing Ligands and Cerium Oxide Nanoparticles.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.57443]

12. Gen-Yi Guo, Ming-Hao Liu, Jing-Ying Yang, Bo Jiang, Ya-Nan Li, Hui-Tao Yu, Hu SHI, Gao-Fei Pan.  (2026)  A recyclable flame-retardant fast-response polyurethane material for fire identification markers.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2026.112035]