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Borane - tert-Butylamine Complex - ≥95.0%, high purity , CAS No.7337-45-3
Basic Description
Synonyms
borane t-butylamine | MFCD00075635 | borane-tert-butylamine | tert-butylamine-borane | FT-0623163 | J-519924 | tert-Butylamine borane | GKFJEDWZQZKYHV-UHFFFAOYSA-N | AMY14898 | B1264 | AKOS015833621 | F14004 | t-butylamine.borane | NSC 114045
Specifications & Purity
≥95%
Storage Temp
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.
Product Description
Reactant involved in: Non-destructive analyses and conservation treatments of Indian drawings; Dehydrogenation reactions mediated by ruthenium bidentate phosphine complexes or ruthenium / iridium bis(N-heterocyclic carbene) complexes; The formation of σ-borane complexes; Ethanolysis of amine-borane adducts to form a reducing system for transfer hydrogenation of terminal olefins; Photochemical hydroboration and oxidation of single-walled carbon nanotubes
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic salts
Class
Organic metal salts
Subclass
Organic metalloid salts
Intermediate Tree Nodes
Not available
Direct Parent
Organic metalloid salts
Alternative Parents
Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aliphatic acyclic compounds
Substituents
Organic metalloid salt - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as organic metalloid salts. These are organic salt compounds containing a metalloid atom in its ionic form.
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.
Names and Identifiers
INCHI
InChI=1S/C4H11N.B/c1-4(2,3)5;/h5H2,1-3H3;
InChIKey
PVYPHUYXKVVURH-UHFFFAOYSA-N
Smiles
[B].CC(C)(C)N
Isomeric SMILES
[B].CC(C)(C)N
WGK Germany
3
RTECS
EO3900000
PubChem CID
6364547
Molecular Weight
86.97
Reaxy-Rn
4134905
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water (27 mg/ml), and methanol
Sensitivity
Moisture & Heat & Air sensitive
Melt Point(°C)
96-98°C
Molecular Weight
83.950 g/mol
XLogP3
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
0
Exact Mass
84.0985 Da
Monoisotopic Mass
84.0985 Da
Topological Polar Surface Area
26.000 Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
25.100
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
Citations of This Product
1.
Xunying Liu, Yun Tang, Leyi Chen, Lei Wang, Yonggang Liu, Zhenghua Tang.
(2024)
Atomically precise Au15Ag23 nanoclusters co-protected by alkynyl and bromine: Structure analysis and electrocatalytic application toward overall water splitting. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,
53
(300).
2.
Zequn Zhang, Yuan Shu, Qian Liu, Shuxian Bi, Pengfei Zhang.
(2023)
Anti-sintering Ni-ZnO catalyst stabilized by a dual protection of SMSI and carbon for efficient RWGS reaction. CHEMICAL ENGINEERING JOURNAL,
475
(146333).
3.
Guo-Dong Yan, Zhen-Hua Zhang, Heng Guo, Jin-Ping Chen, Qing-Song Jiang, Qian-Nan Cui, Zeng-Liang Shi, Chun-Xiang Xu.
(2023)
Exploring plasmons weakly coupling to perovskite excitons with tunable emission by energy transfer. Chinese Physics B,
32
(6):
(67302).
4.
Xinlei Zhang, Xuehua Wang, Guicun Li, Lei Wang, Jianfeng Huang, Alan Meng, Zhenjiang Li.
(2023)
Construction of electron donor–acceptor Z-scheme heterojunction for boosting photocatalytic H2 production. APPLIED SURFACE SCIENCE,
635
(157625).
5.
Yongcheng He, Haohua Liang, Meihua Chen, Licheng Jiang, Zhishen Zhang, Xiaobo Heng, Lin Yang, Yanpeng Hao, Jiulin Gan, Zhongmin Yang.
(2021)
Optical Fiber Waveguiding Soft Photoactuators Exhibiting Giant Reversible Shape Change. Advanced Optical Materials,
9
(21):
(2101132).
6.
Li Huiyong, Hu Dafeng, Zheng Zemin, Jiang Hao, Lu Jiangwei, Geng Xuemin, Zhang Xudong, Wan Yanfen, Yang Peng.
(2020)
Primary growth of binary nanoparticle superlattices with distinct systems contingent on synergy: softness and crystalline anisotropy. Applied Nanoscience,
10
(5):
(1653-1666).
7.
Yun Yang, Shuhua Han, Guangju Zhou, Lijie Zhang, Xingliang Li, Chao Zou, Shaoming Huang.
(2013)
Ascorbic-acid-assisted growth of high quality M@ZnO: a growth mechanism and kinetics study. Nanoscale,
5
(23):
(11808-11819).
8.
Chaoyi Yang, Guangqin Wang, Jianchao Yue, Zihao Dai, Wei Luo.
(2025)
Constructing Ordered Oxophilic Tin Sites on Platinum to Achieve a High-Performance and Anti-CO Poisoning Hydrogen Oxidation Reaction under an Alkaline Electrolyte. ACS Catalysis,
15
(2):
(869-876).
9.
Qingkun Kong, Shuchao Jiang, Zhongyi Wang, Xin Xu, Ruiling Zhang, Guoqing Zhu, Junxia Yang, Peigeng Han, Runze Liu, Feng Hong, Nengchao Luo, Junsheng Chen, Bin Yang.
(2024)
Highly Stable Cesium Molybdenum Chloride Perovskite Nanocrystals for Photothermal Semihydrogenation Applications. ACS Applied Materials & Interfaces,
16
(27):
(35752-35760).
10.
Rui Xu, Yingzhi Sun, Yating Zhu, Fan Wang, Jiayin Wang, Lanjun Cheng, Kaijia Xu, Yinyin Qian.
(2024)
Tunable surface band bending enables switchable photoconductance of colloidal InSb nanowires for self-powered and broadband photodetectors with fast response. APPLIED SURFACE SCIENCE,
670
(160690).
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10 Citations
I2306124