trans-1,4-Cyclohexanedimethanol - ≥98%(GC) , CAS No.3236-48-4

CAS: 3236-48-4 Cat. No.: T162676 Formula: C₈H₁₆O₂ Peso molecolare: 144.21 Beilstein Registry Number: 6(4)5238 Numero EC: 692-674-3

GRADE & PURITY ≥98%(GC)

Synonyms

(4-Hydroxymethylcyclohexyl)methanol | 1,4-Bis(hydroxymethyl)cyclohexane,c&t | Q27259032 | SCHEMBL27912 | 1,4-dihydroxymethylcyclohexane | 1,4-Cyclohexanedimethanol, cis- | 1,4-Cyclohexanedimethanol,c&t | Cyclohexane-1,4-dimethanol,c&t | HSDB 5364 | W-1087

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinonimi

(4-Hydroxymethylcyclohexyl)methanol | 1,4-Bis(hydroxymethyl)cyclohexane,c&t | Q27259032 | SCHEMBL27912 | 1,4-dihydroxymethylcyclohexane | 1,4-Cyclohexanedimethanol, cis- | 1,4-Cyclohexanedimethanol,c&t | Cyclohexane-1,4-dimethanol,c&t | HSDB 5364 | W-1087

Specifiche e purezza

≥98%(GC)

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normal

Purezza

≥98%(GC)

Nomi e identificatori

• Pubchem Sid: 488180546
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180546
• Sorrisi canonici: C1CC(CCC1CO)CO
• IUPAC Name: [4-(hydroxymethyl)cyclohexyl]methanol
• InChIKey: YIMQCDZDWXUDCA-UHFFFAOYSA-N
• INCHI: 1S/C8H16O2/c9-5-7-1-2-8(6-10)4-3-7/h7-10H,1-6H2
• Isomeri SMILES: C1CC(CCC1CO)CO
• Peso molecolare: 144.21
• Beilstein: 6(4)5238
• Reaxy-Rn: 1902271
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1902271&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Alcohols and polyols
• Intermediate Tree Nodes: Not available
• Direct Parent: Primary alcohols
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Hydrocarbon derivative - Primary alcohol - Aliphatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).
• 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

• Solubilità: Soluble in Methanol
• Sensibilità: Hygroscopic
• Punto di ebollizione (°C): 164 °C/12 mmHg
• Punto di fusione (°C): 67 °C
• Peso molecolare: 144.210 g/mol
• XLogP3: 0.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 144.115 Da
• Monoisotopic Mass: 144.115 Da
• Topological Polar Surface Area: 40.500 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 73.300
• 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. Zhili Chang, Boyong Ye, Zixin Zhong, Songlin Wang, Han Wang, Weichen Du, Zhaoyin Hou.  (2023)  Synthesis of Cu1Mg3Sc2(OH)12CO3 layered double hydroxide and its derived catalyst for hydrogenation of DMCD to CHDM.  Journal of Materials Chemistry A,  12  (2): (1003-1011).  [PMID:] [10.1039/D3TA06081K]

2. Jinggang Wang, Xiaoqin Zhang, Xuan Fei, Ruixue Gao, Fei Liu, Lin Fan, Jin Zhu, Xiaoqing Liu.  (2022)  Synthesis of High Thermal-Resistant Poly(ester-ether) Elastomers from Bio-Based 2,5-Furandicarboxylic Acid.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.2c02751]

3. Shengdi Yan, Guozhang Wu.  (2022)  Thermo-induced chain scission and oxidation of isosorbide-based polycarbonates: Degradation mechanism and stabilization strategies.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2022.110028]

4. Zhen Jia, Jinggang Wang, Liyuan Sun, Fei Liu, Jin Zhu, Xiaoqing Liu.  (2018)  Copolyesters developed from bio-based 2,5-furandicarboxylic acid: Synthesis, sequence distribution, mechanical, and barrier properties of poly(propylene-co-1,4-cyclohexanedimethylene 2,5-furandicarboxylate)s.  JOURNAL OF APPLIED POLYMER SCIENCE,  136  (13): (47291).  [PMID:] [10.1002/app.47291]

5. Zhihao Zhang, Zhiyuan Yao, Yujing He, Senlong Yu, Meijia Chen, Zhenjiang Shi, Jiaxu He, Hengxue Xiang, Meifang Zhu.  (2024)  Melt-spun poly(ethylene terephthalate-co-1,4-cyclohexanedimethylene terephthalate) (PETG) copolyester fibers: Synergistic effect of chemical and crystal structure regulation.  POLYMER ENGINEERING AND SCIENCE,      [PMID:] [10.1002/pen.27040]

6. Shen Wang, Liying Guo, Xiang Li, Shirui Xu.  (2025)  Preparation of Copolyester PESG and Its Properties by CHDM Modified PES.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.70020]