Triethylphosphine - 1.0 M in THF , CAS No.554-70-1

CAS: 554-70-1 Cat. No.: T120625 Peso molecular: 118.16 Beilstein Registry Number: 969170 Número EC: 209-068-8 PubChem CID: 27365
Disponible para pedir
GRADE & PURITY 1.0 M in THF
Synonyms
BCP04420 | InChI=1/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H | UNII-5W435D16PM | Et3P | Tl409 | GC10086 | Q27104454 | BP-30174 | Triethylphosphine, 99% | TRIETHYLPHOSPHINE [MI] | AMY11700 | CHEBI:39971 | Phosphorus triethyl | MFCD00009256 | EINECS 209-068-8 | PEt
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10ml
T120625-10ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
86,90US$
50ml
T120625-50ml
1
331,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

1.0 M in THF for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Application

Catalyst for:

Regioselective formation of alcohols from hydrocarbonylation of alkenes

Bronsted acid-assisted synthesis of dihydropyrones from aromatic aldehydes and allenoates

Silaboration of enynes

Conversion of phenylacetic acids to phenylacetonitriles of benzonitriles

Thermal decomposition of platinum and palladium naphthalenediyl

Asymmetrical Morita-Baylis-Hillman reaction

Specifications

Sinónimos
BCP04420 | InChI=1/C6H15P/c1-4-7(5-2)6-3/h4-6H2, 1-3H | UNII-5W435D16PM | Et3P | Tl409 | GC10086 | Q27104454 | BP-30174 | Triethylphosphine, 99% | TRIETHYLPHOSPHINE [MI] | AMY11700 | CHEBI:39971 | Phosphorus triethyl | MFCD00009256 | EINECS 209-068-8 | PEt
Especificaciones y pureza
1.0 M in THF
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Nombres e identificadores
Sonrisas canónicasCCP(CC)CC
IUPAC Nametriethylphosphane
InChIKeyRXJKFRMDXUJTEX-UHFFFAOYSA-N
INCHI1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
Isómeros SMILES CCP(CC)CC
WGK Alemania 3
RTECS SZ3400000
PubChem CID 27365
Número ONU 2845
Peso molecular 118.16
Beilstein 969170

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganophosphorus compounds
ClaseOrganic phosphines and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentOrganic phosphines and derivatives
Alternative Parents Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Phosphine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescripciónThis 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 tertiary phosphine
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeFechaArticulo
B2604386Certificate of AnalysisFeb 06, 2026 T120625
E2413535Certificate of AnalysisFeb 05, 2026 T120625
E2512471Certificate of AnalysisMay 16, 2025 T120625
E2413534Certificate of AnalysisMay 28, 2024 T120625
A2330962Certificate of AnalysisFeb 02, 2023 T120625
Propiedades químicas y físicas
SensibilidadAir sensitive.Moisture sensitive.
Punto de inflamación (°F)-4 °F
Punto de inflamación (°C)-17 °C
Punto de ebullición (°C)127-128°C
Peso molecular118.160 g/mol
XLogP31.000
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count3
Exact Mass118.091 Da
Monoisotopic Mass118.091 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count7
Formal Charge0
Complexity25.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Xiaofei Shen, Hailong Huang, Hao Qian, Longxiang Tang, Yan Zhang, Min Xu, Huiqing Wang, Zhongkai Wang.  (2021)  Super Chirality Promotion of Helical Poly(Phenyl Isocyanide)s by Grafting onto Ethyl Cellulose.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  222  (15): (2100103).  [PMID:] [10.1002/macp.202100103]
2. Hao Qian, Xiaofei Shen, Hailong Huang, Yan Zhang, Mingtao Zhang, Huiqing Wang, Zhongkai Wang.  (2019)  Helical poly(phenyl isocyanide)s grafted selectively on C-6 of cellulose for improved chiral recognition ability.  CARBOHYDRATE POLYMERS,      [PMID:31888853] [10.1016/j.carbpol.2019.115737]
3. Xinrong Li, Shuliang Chen, Peng Yang, Yue Lin, Chen Chen, Xianzhi Hu, Futing Zi.  (2024)  Effective and selective recovery of Au(III) from WPCBs using quaternary phosphonium adsorbent synthesized by adjusting steric hindrance.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:38878433] [10.1016/j.jhazmat.2024.134881]
4. Li He, Ciping Chen, Yongge Liu, Hong Hai, Jianping Li.  (2023)  Ultrasensitive detect of CA125 based on triple signal amplification strategy with huge amount of loaded probes via exonuclease cyclic cleavage, rolling cyclic amplification and strand self-growth.  ANALYST,      [PMID:37323073] [10.1039/D3AN00414G]
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