Triphenyl phosphite - ≥98% , CAS No.101-02-0

CAS: 101-02-0 Cat. No.: T104038 Peso molecular: 310.28 Beilstein Registry Number: 1079456 Número EC: 202-908-4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Trifenylfosfit [Czech] | Tris(phenoxy)phosphine | DTXSID0026252 | EINECS 202-908-4 | NSC-62219 | Mellite 310 | AI3-07866 | Trifenoxyfosfin | DTXCID306252 | Triphenyl Phosphite (TPPi) | Weston TPP | ADK Stab TPP | NCIOpen2_007800 | JP 360 | Trifenoxyfosfin
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100g
T104038-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
9,90US$
500g
T104038-500g
3
22,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

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

📚

Literature proof

Cited in 35 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Used to convert alcohols to alkyl halides, as a peptide coupling agent, and, in combination with ozone, as a low-temperature source of singlet oxygen, and ligand for metal-catalyzed reactions.


application:

Triphenyl phosphite can be used:

As a source of phosphorus and as a ligand for the synthesis of transition metal phosphide nanoparticles via heating-up process.

To convert alcohols to alkyl halides.

As a peptide coupling agent.

As a low-temperature source of singlet oxygen after forming an adduct with ozone.

To synthesize bromotriphenoxyphosphonium bromide, a brominating agent, by reacting with bromine.

Specifications

Sinónimos
Trifenylfosfit [Czech] | Tris(phenoxy)phosphine | DTXSID0026252 | EINECS 202-908-4 | NSC-62219 | Mellite 310 | AI3-07866 | Trifenoxyfosfin | DTXCID306252 | Triphenyl Phosphite (TPPi) | Weston TPP | ADK Stab TPP | NCIOpen2_007800 | JP 360 | Trifenoxyfosfin
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504751386
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751386
Sonrisas canónicasC1=CC=C(C=C1)OP(OC2=CC=CC=C2)OC3=CC=CC=C3
IUPAC Nametriphenyl phosphite
InChIKeyHVLLSGMXQDNUAL-UHFFFAOYSA-N
INCHI1S/C18H15O3P/c1-4-10-16(11-5-1)19-22(20-17-12-6-2-7-13-17)21-18-14-8-3-9-15-18/h1-15H
Isómeros SMILES C1=CC=C(C=C1)OP(OC2=CC=CC=C2)OC3=CC=CC=C3
WGK Alemania 2
RTECS TH1575000
Número ONU 3077
Grupo de embalaje III
Peso molecular 310.28
Beilstein 1079456
Reaxy-Rn 1079456

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
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassPhenoxy compounds
Intermediate Tree Nodes Not available
Direct ParentPhenoxy compounds
Alternative Parents Organic phosphites  Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenoxy compound - Organic phosphite - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
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.

36 results found

Lot NumberCertificate TypeFechaArticulo
D2616452Certificate of AnalysisApr 24, 2026 T104038
D2616454Certificate of AnalysisApr 24, 2026 T104038
D2616453Certificate of AnalysisApr 24, 2026 T104038
D2616455Certificate of AnalysisApr 24, 2026 T104038
D2616451Certificate of AnalysisApr 24, 2026 T104038
D2616447Certificate of AnalysisApr 23, 2026 T104038
D2616448Certificate of AnalysisApr 23, 2026 T104038
D2616449Certificate of AnalysisApr 23, 2026 T104038
C2627456Certificate of AnalysisApr 17, 2026 T104038
C2627459Certificate of AnalysisApr 17, 2026 T104038
C2627681Certificate of AnalysisApr 17, 2026 T104038
C2627455Certificate of AnalysisApr 17, 2026 T104038
C2627458Certificate of AnalysisApr 17, 2026 T104038
C2627680Certificate of AnalysisApr 17, 2026 T104038
A2606508Certificate of AnalysisJan 16, 2026 T104038
H2514087Certificate of AnalysisAug 27, 2025 T104038
F2528104Certificate of AnalysisJul 11, 2025 T104038
F2509084Certificate of AnalysisJun 16, 2025 T104038
D2509098Certificate of AnalysisApr 18, 2025 T104038
K21111070Certificate of AnalysisAug 03, 2023 T104038
K21111072Certificate of AnalysisAug 03, 2023 T104038
I2114004Certificate of AnalysisJun 13, 2023 T104038
I2111026Certificate of AnalysisJun 13, 2023 T104038
I2114005Certificate of AnalysisJun 13, 2023 T104038
H2104371Certificate of AnalysisMay 10, 2023 T104038
K2222362Certificate of AnalysisJun 11, 2022 T104038
B2525040Certificate of AnalysisJun 11, 2022 T104038
J2211203Certificate of AnalysisJun 11, 2022 T104038
J2211202Certificate of AnalysisJun 11, 2022 T104038
J2211201Certificate of AnalysisJun 11, 2022 T104038
J2211197Certificate of AnalysisJun 11, 2022 T104038
I2308199Certificate of AnalysisJun 11, 2022 T104038
I2308196Certificate of AnalysisJun 11, 2022 T104038
I2308194Certificate of AnalysisJun 11, 2022 T104038
D2502105Certificate of AnalysisJun 11, 2022 T104038
F2129391Certificate of AnalysisJun 11, 2021 T104038

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Propiedades químicas y físicas
SolubilidadInsoluble in water
SensibilidadMoisture Sensitive ,air sensitive
Punto de congelación (°C)20 °C
Índice de refracción1.59
Punto de inflamación (°F)410 °F
Punto de inflamación (°C)206℃
Punto de ebullición (°C)360°C
Punto de fusión (°C)22-24°C
Peso molecular310.300 g/mol
XLogP35.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count6
Exact Mass310.076 Da
Monoisotopic Mass310.076 Da
Topological Polar Surface Area27.700 Ų
Heavy Atom Count22
Formal Charge0
Complexity247.000
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
Citations of This Product
Referencias
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16. Xing-Zhou Lu, Chao Gu, Qi Zhang, Lei Shi, Shi-Kui Han, Guan-Ping Jin.  (2021)  Regioselective Construction of Chemically Transformed Phosphide–Metal Nanoheterostructures for Enhanced Hydrogen Evolution Catalysis.  INORGANIC CHEMISTRY,      [PMID:33764054] [10.1021/acs.inorgchem.1c00348]
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18. Pan Zhaoqun, Chen Mianfeng, Zeng Keling, Kang Yingzi.  (2021)  Synthesis of Epoxy-Modified Methyl Phenyl Silicone Resins for LED Encapsulation.  Silicon,  14  (3): (1159-1167).  [PMID:] [10.1007/s12633-020-00868-6]
19. Canhuang Li, Siyong Wu, Yijing Qiu, Dongsheng Lu.  (2020)  Phosphorus-Containing C12H27O4P as Functional Electrolyte Additives for High-Voltage LiNi0.5Mn1.5O4/Graphite Li-Ion Batteries with Excellent Electrochemical Performance.  Advanced Materials Interfaces,  (3): (2001588).  [PMID:] [10.1002/admi.202001588]
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