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Tri-tert-butylphosphine solution - 1.0 M in 2-methyltetrahydrofuran, high purity , CAS No.13716-12-6

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Tri-tert-butylphosphine solution - 1.0 M in 2-methyltetrahydrofuran, high purity , CAS No.13716-12-6

6 Citations

COA

Grade & Purity:

1.0 M in 2-methyltetrahydrofuran

Cas Number: 13716-12-6
Molecular Weight: 202.32
Beilstein Registry Number: 1738613
EC Number: 237-266-4
PubChem CID: 83681

In stock

Item Number

T431998

Grouped product items
SKU	Size	Availability	Price	Qty
T431998-25ml	25ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$686.90

Basic Description

Synonyms	doi:10.14272/BWHDROKFUHTORW-UHFFFAOYSA-N.1 \| EINECS 237-266-4 \| tri tert-butylphosphane \| Tri-tert-butylphosphine, 90%, technical grade \| InChI=1/C12H27P/c1-10(2,3)13(11(4,5)6)12(7,8)9/h1-9H \| monochloro-1,4-dimethoxybenzene \| SCHEMBL28566 \| tri-tert.buty
Specifications & Purity	1.0 M in 2-methyltetrahydrofuran
Product Description	Application Valuable ligand for several coupling reactions. This product is offered as a solution in 2-methyltetrahydrofuran for more convenient handling.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organophosphorus compounds
  - Class Organic phosphines and derivatives

Kingdom	Organic compounds
Superclass	Organophosphorus compounds
Class	Organic phosphines and derivatives
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organic phosphines and derivatives
Alternative Parents	Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Phosphine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as organic phosphines and derivatives. These are organic compounds containing a phosphine derivative, with the general formula B1P(R2)R3 (R1-R3=alkyl, aryl).
External Descriptors	Not available
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

Names and Identifiers

IUPAC Name	tritert-butylphosphane
INCHI	InChI=1S/C12H27P/c1-10(2,3)13(11(4,5)6)12(7,8)9/h1-9H3
InChIKey	BWHDROKFUHTORW-UHFFFAOYSA-N
Smiles	CC(C)(C)P(C(C)(C)C)C(C)(C)C
Isomeric SMILES	CC(C)(C)P(C(C)(C)C)C(C)(C)C
WGK Germany	3
PubChem CID	83681
UN Number	2845
Molecular Weight	202.32
Beilstein	1738613

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Flash Point(°F)	39.2 °F
Flash Point(°C)	-17 °C
Boil Point(°C)	102-103°C
Melt Point(°C)	30-35°C
Molecular Weight	202.320 g/mol
XLogP3	2.900
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	3
Exact Mass	202.185 Da
Monoisotopic Mass	202.185 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	128.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Jie Xie, Xiaobing Wang, Yonghui Wang, Jiawei Li, Chun Cao, Ming Jin. (2024) Effect of substituents on the performance of N-carbazolyl double benzylidene ketones in visible/NIR light one/two-photon polymerization. EUROPEAN POLYMER JOURNAL, 202 (112636).
2. Xianqi Zhu, Lin Li, Jin Tang, Chunyu Yang, Hao Yu, Kunpeng Liu, Ziyan Zheng, Xinggui Gu, Qingsong Yu, Fu-Jian Xu, Zhihua Gan. (2022) Cascade-responsive nano-assembly for efficient photothermal-chemo synergistic inhibition of tumor metastasis by targeting cancer stem cells. BIOMATERIALS, 280 (121305).
3. Shuailing Huang, Yinglong Wu, Fang Zeng, Junjie Chen, Shuizhu Wu. (2018) A turn-on fluorescence probe based on aggregation-induced emission for leucine aminopeptidase in living cells and tumor tissue. ANALYTICA CHIMICA ACTA, 1031 (169).
4. Ruming Jiang, Meiying Liu, Hongye Huang, Long Huang, Qiang Huang, Yuanqing Wen, Qian-yong Cao, Jianwen Tian, Xiaoyong Zhang, Yen Wei. (2018) A novel self-catalyzed photoATRP strategy for preparation of fluorescent hydroxyapatite nanoparticles and their biological imaging. APPLIED SURFACE SCIENCE, 434 (1129).
5. Shuailing Huang, Yinglong Wu, Fang Zeng, Lihe Sun, Shuizhu Wu. (2016) Handy ratiometric detection of gaseous nerve agents with AIE-fluorophore-based solid test strips. Journal of Materials Chemistry C, 4 (42): (10105-10110).
6. Lihuan Xu, Qiang Fei, Lin Yao, Chang Su. (2024) Triphenylamine-containing dihydrophenazine copolymers with adjustable multi-electron redox characteristics and their application as cathodes in lithium-organic batteries. Journal of Materials Chemistry A, 12 (22): (13320-13327).

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