Borane - Morpholine Complex - ≥95%(GC) , CAS No.4856-95-5

CAS: 4856-95-5 Cat. No.: B135840 Molecular Weight: 100.96 EC Number: 225-450-7 PubChem CID: 6327109

GRADE & PURITY ≥95%(GC)

Synonyms

Borane, compound with morpholine | Morpholineborane | NSC 93813 | Boron, trihydro(morpholine-.kappa.N4)-, (T-4)- | Trihydro(morpholine-N4)boron | AKOS025311064 | BS-42302 | NCGC00357171-01 | F14226 | DTXCID2030693 | DTXSID0052124 | FT-0623162 | AMY14878 |

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

Reactant involved in:Ethanolysis producing a reducing system; Being a reducing agent for synthesis of Rh nanoparticle / carbon nanotube catalysts;Stereoselective and regioselective reduction of steroidal ketones; Methanolic cleavage4

Specifications

Synonyms

Borane, compound with morpholine | Morpholineborane | NSC 93813 | Boron, trihydro(morpholine-.kappa.N4)-, (T-4)- | Trihydro(morpholine-N4)boron | AKOS025311064 | BS-42302 | NCGC00357171-01 | F14226 | DTXCID2030693 | DTXSID0052124 | FT-0623162 | AMY14878 |

Specifications & Purity

≥95%(GC)

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%(GC)

Names and Identifiers

• Canonical Smiles: [B].C1COCCN1
• InChIKey: YJROYUJAFGZMJA-UHFFFAOYSA-N
• INCHI: 1S/C4H9NO.B/c1-3-6-4-2-5-1;/h5H,1-4H2
• Isomeric SMILES: [B].C1COCCN1
• WGK Germany: 3
• RTECS: QD8530000
• PubChem CID: 6327109
• Molecular Weight: 100.96
• Reaxy-Rn: 13732283

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Oxazinanes
      • Subclass Morpholines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Oxazinanes
• Subclass: Morpholines
• Intermediate Tree Nodes: Not available
• Direct Parent: Morpholines
• Alternative Parents: Oxacyclic compounds Organic metalloid salts Dialkylamines Dialkyl ethers Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Morpholine - Dialkyl ether - Secondary aliphatic amine - Ether - Secondary amine - Organic metalloid salt - Azacycle - Oxacycle - Organooxygen compound - Amine - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
• 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

Chemical and Physical Properties

• Solubility: Slightly soluble in water,Decomposes in contact with water
• Sensitivity: Moisture Sensitive
• Melt Point(°C): 96-99℃
• Molecular Weight: 97.930 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 98.0777 Da
• Monoisotopic Mass: 98.0777 Da
• Topological Polar Surface Area: 21.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 34.500
• 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: 2

XLogP3

References

1. Xianhua Mao, Ziyu Li, Yijia Liu, Xiuxiu Nie, Benzhang Li, Qinglin Jiang, Chunmei Gao, Yuan Gao, Lei Wang.  (2020)  Tuning the structure of borane-nitrogen derivatives towards high-performance carbon nanotubes-based n-type thermoelectric materials.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2020.126616]

2. Sisi Yang, Zhenglin Li, Yuanlin Wang, Xuelei Fan, Zhaohua Miao, Ying Hu, Zhuo Li, Ye Sun, Flemming Besenbacher, Miao Yu.  (2018)  Multifunctional Bi@PPy-PEG Core–Shell Nanohybrids for Dual-Modal Imaging and Photothermal Therapy.  ACS Applied Materials & Interfaces,      [PMID:29272573] [10.1021/acsami.7b17838]

3. Feng Jiang, Jian Cai, Bing Liu, Yuebing Xu, Xiaohao Liu.  (2016)  Particle size effects in the selective hydrogenation of cinnamaldehyde over supported palladium catalysts.  RSC Advances,  6  (79): (75541-75551).  [PMID:] [10.1039/C6RA17000E]

4. Qing Zeng, Mengyuan Ma, Hui Liu, Lin Xu, Shaonan Tian, Dong Chen, Jing Wang, Jun Yang.  (2025)  Gold-catalyzed construction of atomically rough surfaces towards high-efficiency ethanol electrooxidation.  Science Bulletin,      [PMID:40348670] [10.1016/j.scib.2025.04.051]

5. Xijie Qu, Tong Liu, Yu Wang, Xinyuan Wei, Ye Yang, Liya Gu, Kun Yang, Jing Zhang, Yan Liu, Yiqian Liang, Yanzhen Zheng, Aimin Yang.  (2026)  Multifunctional Bismuth Nanoplatforms Augment Radioactive Iodine Therapy in Anaplastic Thyroid Cancer.  International Journal of Nanomedicine,      [PMID:] [10.2147/IJN.S561413]