6-Amino-1-hexanol - ≥97% , CAS No.4048-33-3

CAS: 4048-33-3 Cat. No.: A101232 Peso molecular: 117.19 Beilstein Registry Number: 1732524 Número EC: 223-748-1

GRADE & PURITY ≥97%

Synonyms

SY003099 | 6-Amino-1-hexanol, purum, >=97.0% (NT) | aminohexan-6-ol | H2NCH2(CH2)4CH2OH | NH2(CH2)6OH | 1-Hexanol, 6-amino- | 6-Amino-1-hexanol | 6-Aminohexanol | BP-20654 | DTXSID9075242 | MFCD00008241 | rac 5-Hydroxy Valproic Acid-d7 Sodium Salt | HY-W0

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

6-Amino-1-hexanol can undergo cyclization over copper supported on γ-alumina and magnesia to form hexahydro-1H-azepine. It may be used along with glutaric acid to generate poly(ester amide)s with excellent film- and fiber forming properties.

Specifications

Sinónimos

SY003099 | 6-Amino-1-hexanol, purum, >=97.0% (NT) | aminohexan-6-ol | H2NCH2(CH2)4CH2OH | NH2(CH2)6OH | 1-Hexanol, 6-amino- | 6-Amino-1-hexanol | 6-Aminohexanol | BP-20654 | DTXSID9075242 | MFCD00008241 | rac 5-Hydroxy Valproic Acid-d7 Sodium Salt | HY-W0

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488182577
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182577
• Sonrisas canónicas: C(CCCO)CCN
• IUPAC Name: 6-aminohexan-1-ol
• InChIKey: SUTWPJHCRAITLU-UHFFFAOYSA-N
• INCHI: 1S/C6H15NO/c7-5-3-1-2-4-6-8/h8H,1-7H2
• Isómeros SMILES: C(CCCO)CCN
• WGK Alemania: 3
• RTECS: MO8840000
• Peso molecular: 117.19
• Beilstein: 1732524
• Reaxy-Rn: 1732524
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732524&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkanolamines
• Alternative Parents: Primary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkanolamine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alkanolamines. These are organic compounds that carry a hydroxy and an amino functional groups on an alkane backbone.
• 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: Soluble in water.
• Sensibilidad: Moisture sensitive
• Punto de inflamación (°F): 133℃(271°F)
• Punto de inflamación (°C): 133℃(271°F)
• Punto de ebullición (°C): 225°C
• Punto de fusión (°C): 55-58°C
• Peso molecular: 117.190 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 117.115 Da
• Monoisotopic Mass: 117.115 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 39.500
• 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. Fen Zheng, Jianghuan Shi, Shanming Zhang, Kaige Liu, Long Xu.  (2023)  A New Biodegradable Linear mPEG-b-poly(Schiff Base-Acetal) Copolymer Carrier Co-Delivery Cinnamaldehyde and Gemcitabine for Combined Anticancer Therapy.  ChemistrySelect,  8  (29): (e202301647).  [PMID:] [10.1002/slct.202301647]

2. Jialiang Kang, Xueting Wang, Xiaoxiang He, Cun Lv, Caixia He, Zhanxiong Li.  (2023)  Preparation of hydrophobic block copolymer PCL-b-PFPE: The microsphere-coated fabrics via direct electrostatic spraying and its super-hydrophobicity.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2022.107395]

3. Jie Liu, Si-Yu Gao, Xin-Yi Zhang, Yakai Feng, Han-Chun Wu, Zhijian Chen, Maxim V. Bermeshev, Xiang-Kui Ren.  (2022)  POSS-containing polynorbornene with pendant perylene diimide: from a unique supramolecular structure to tunable luminescence properties.  Journal of Materials Chemistry C,  10  (22): (8791-8796).  [PMID:] [10.1039/D2TC01487D]

4. Yujie Zhang, Min Chen, Shouyong Zhou, Haifeng Han, Mingliang Zhang, Hongdeng Qiu.  (2021)  A carbonylative coupling approach to alkyl stationary phases with variable embedded carbamate groups for high-performance liquid chromatography.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:34875517] [10.1016/j.chroma.2021.462718]

5. Haipeng Wang, Wulong Li, Zhanxiong Li.  (2018)  Preparation of fluorinated PCL porous microspheres and a super-hydrophobic coating on fabrics via electrospraying.  Nanoscale,  10  (39): (18857-18868).  [PMID:30277254] [10.1039/C8NR05793A]

6. Ming Wang, Qi-jian Zhang, Zhuang Li, Hua Li, Jian-Mei Lu.  (2018)  Solvents Effects on Film Morphologies and Memory Behavior of a Perylenediimide-Containing Pendent Polymer.  Chemistry-An Asian Journal,  13  (14): (1784-1790).  [PMID:29741817] [10.1002/asia.201800331]

7. Bing Wang, Ping Chen, Ji Zhang, Xiao-Chuan Chen, Yan-Hong Liu, Zheng Huang, Qing-Ying Yu, Ju-Hui Zhang, Wei Zhang, Xi Wei, Xiao-Qi Yu.  (2017)  Self-assembled core–shell-corona multifunctional non-viral vector with AIE property for efficient hepatocyte-targeting gene delivery.  Polymer Chemistry,  8  (48): (7486-7498).  [PMID:] [10.1039/C7PY01520H]

8. Rong-Fu Huang, Liu-Ting Wang, Qi-Qi Gai, Dong-Mei Wang, Lei Qian.  (2017)  DNA-mediated assembly of carbon nanotubes for enhancing electrochemiluminescence and its application.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2017.10.033]

9. Meijia Gong, Luping Wang, Kaiyang Hou, Kaiqiang Zhang, Xu Wang.  (2025)  Mastering Hydrogen Bonding at Hard–Soft Interfaces for Ultrahigh Damage Resistance in Elastomers.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.5c00002]

10. Chang-An Xu, Xingchi Li, Zhengbang Tong, Zhuangzhuang Chu, Heng Fang, Yang Hu, Xudong Chen, Zhuohong Yang.  (2024)  Mimosa inspired intelligent anti-corrosive composite coating by incorporating lignin and pyridine derivatives grafted graphene oxide.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.149316]

11. Ge Zhi-Qing, Yan Shuo, Pan Zu-Xiong, Lei Shan, Mao Xuan-Zhi, Zhao Chu, Wang Mo-Zhen, Ge Xue-Wu.  (2024)  Preparation and Structure-Property Regulation Mechanism of Reversible Thermochromic Polydiacetylene.  CHINESE JOURNAL OF POLYMER SCIENCE,      [PMID:] [10.1007/s10118-024-3142-4]

12. Nengde Liang, Jingyue Li, YingJian Chen, Miao Zhang, Bin Xie, Zelin Sun, Liu Zhong, Qiwei Wang, Wai-Yeung Wong.  (2025)  Norbornenyl-Modified Nanosilica for Reinforced Polydicyclopentadiene Composites.  POLYMER COMPOSITES,      [PMID:] [10.1002/pc.70177]

13. Dan-Li Hao, Ran Xie, Ge-Jing De, Hong Yi, Chen Zang, Mi-Yi Yang, Li Liu, Hai Ma, Wei-Yan Cai, Qing-He Zhao, Feng Sui, Yan-Jun Chen.  (2020)  pH-Responsive Artesunate Polymer Prodrugs with Enhanced Ablation Effect on Rodent Xenograft Colon Cancer.  International Journal of Nanomedicine,      [PMID:32214810] [10.2147/IJN.S242032]

14. Siqi Liu, Yinfang Zhang, Yifan Ge, Hairui Deng, Jin Wen, Yangju Lin, Yinjun Chen, Meifang Zhu.  (2026)  Visualization of Polymer Chain Alignment in Fiber Spinning and Hot Stretching by Noncovalent Polymer Mechanochemistry.  CHEMISTRY OF MATERIALS,      [PMID:] [10.1021/acs.chemmater.5c02814]

15. Yiqing Wang, Jingkai Liu, Ziyu Liu, Jinyue Dai, Xiaoqing Liu.  (2026)  Sustainable benzoxazine-based phase change materials: from bio-based to upcycling.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2026.114787]