Tri-o-cresyl Phosphate - ≥96% , CAS No.78-30-8

CAS: 78-30-8 Cat. No.: T121610 Peso molecular: 368.37 Número EC: 201-103-5
Disponible para pedir
GRADE & PURITY ≥96%
Synonyms
o-Tolyl phosphate;TOCP | Tri-2-methylphenyl phosphate | DTXCID4012192 | CCRIS 6421 | SB66654 | Tri 2-methylphenyl phosphate | CAS-78-30-8 | CAS_78-30-8 | Phosphoric acid, tri(2-tolyl)ester | SCHEMBL35762 | Phosphoric acid, tri-o-tolyl ester | BCP30457 | E
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
T121610-1g
2
9,90US$
5g
T121610-5g
1
29,90US$
25g
T121610-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
59,90US$
100g
T121610-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
149,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Tri-o-tolyl phosphate is classified under the class of non-halogenated organophosphate esters (OPE)
Purpose
Tri-o-tolyl phosphate may be used as an analytical reference standard for the determination of tri-o-tolyl phosphate in:
Analysis of tri-o-tolyl phosphate in edible oils by TLC and GC is described in methods FSSAI 02.036:2021 and FSSAI 02.037:2021
Surface water and wastewater effluent samples by liquid chromatography coupled to tandem mass spectrometry equipped with electrospray ionization (LC-ESI-MS/MS) operating under the multiple reaction monitoring (MRM) mode of detection.
Human hair and nails by liquid-liquid extraction (LLE) and gas chromatography-mass spectrometry (GC-MS).
Indoor air, dust and window wipes by GC-MS/MS
Outdoor air samples by ultra-performance liquid chromatography coupled to triple quadrupole mass spectrometry (UPLC-QqQ-MS/MS) equipped with ESI source and MRM detection

Specifications

Sinónimos
o-Tolyl phosphate;TOCP | Tri-2-methylphenyl phosphate | DTXCID4012192 | CCRIS 6421 | SB66654 | Tri 2-methylphenyl phosphate | CAS-78-30-8 | CAS_78-30-8 | Phosphoric acid, tri(2-tolyl)ester | SCHEMBL35762 | Phosphoric acid, tri-o-tolyl ester | BCP30457 | E
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥96%
Nombres e identificadores
Pubchem Sid504751112
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751112
Sonrisas canónicasCC1=CC=CC=C1OP(=O)(OC2=CC=CC=C2C)OC3=CC=CC=C3C
IUPAC Nametris(2-methylphenyl) phosphate
InChIKeyYSMRWXYRXBRSND-UHFFFAOYSA-N
INCHI1S/C21H21O4P/c1-16-10-4-7-13-19(16)23-26(22,24-20-14-8-5-11-17(20)2)25-21-15-9-6-12-18(21)3/h4-15H,1-3H3
Isómeros SMILES CC1=CC=CC=C1OP(=O)(OC2=CC=CC=C2C)OC3=CC=CC=C3C
RTECS TD0350000
Número ONU 2574
Grupo de embalaje II
Peso molecular 368.37
Reaxy-Rn 1892885

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
SuperclassOrganic acids and derivatives
ClaseOrganic phosphoric acids and derivatives
SubclassPhosphate esters
Intermediate Tree Nodes Aryl phosphates
Direct ParentAryl phosphotriesters
Alternative Parents Phenoxy compounds  Toluenes  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aryl phosphotriester - Phenoxy compound - Toluene - Benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aryl phosphotriesters. These are aryl phosphates in which the phosphate is esterified at exactly three positions.
External Descriptors Not available
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
K2512557Certificate of AnalysisOct 11, 2025 T121610
K2512559Certificate of AnalysisOct 11, 2025 T121610
K2512565Certificate of AnalysisOct 11, 2025 T121610
K2129303Certificate of AnalysisSep 08, 2025 T121610
K2316354Certificate of AnalysisNov 06, 2023 T121610
K2316355Certificate of AnalysisNov 06, 2023 T121610
I1510100Certificate of AnalysisMay 06, 2023 T121610
Propiedades químicas y físicas
SolubilidadInsoluble in water; Soluble in Ether,Alcohol
SensibilidadLight sensitive
Índice de refracción1.56
Punto de inflamación (°F)230.0 °F
Punto de inflamación (°C)110 °C
Punto de ebullición (°C)410°C
Peso molecular368.400 g/mol
XLogP36.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count6
Exact Mass368.118 Da
Monoisotopic Mass368.118 Da
Topological Polar Surface Area44.800 Ų
Heavy Atom Count26
Formal Charge0
Complexity416.000
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
1. Yijing Wu, Wenjun Zheng, Canrong Chen, Linyan Yang, Ping Tong, Yanhui Zhong, Zian Lin, Zongwei Cai.  (2023)  Facile synthesis of spherical covalent organic frameworks for enrichment and quantification of aryl organophosphate esters in mouse serum and tissues.  JOURNAL OF SEPARATION SCIENCE,  46  (22): (2300482).  [PMID:37727055] [10.1002/jssc.202300482]
2. Xun’e Yi, Haiyu Qin, Guangyu Li, Ren Kong, Chunsheng Liu.  (2024)  Isomer-specific cardiotoxicity induced by tricresyl phosphate in zebrafish embryos/larvae.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:38823104] [10.1016/j.jhazmat.2024.134753]
3. Xiangsheng Tian, Yiquan Ou, Shengyuan Shi, Qiuhua Zhou, Sihong Long, Yao Xiang, Weichao Zhao, Dingxin Long.  (2024)  SIRT1-Dependent Neuroprotection by Resveratrol in TOCP-Induced Spinal Cord Injury: Modulation of ER Stress and Autophagic Flux.  Toxics,  12  (11): (810).  [PMID:39590990] [10.3390/toxics12110810]
4. Zelin Zhu, Xiuping Qi, Zhihao Zhang, Xuanyu Dou, Xinxin Jiang, Yutong Liu, Shencheng Fu, Xintong Zhang, Yichun Liu.  (2024)  Ultra-High Secure Holographically Steganographic Array with Spatiotemporal Dual-Encryption Keys.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202414352]
5. Sangping Li, Shule Tan, Xiangsheng Tian, Yiquan Ou, Shujuan Hu, Weichao Zhao, Dingxin Long.  (2025)  Resveratrol mitigates TOCP-induced spinal cord neurotoxicity by suppressing ferroptosis, a process mediated through the p62/Keap1/Nrf2 pathway.  TOXICOLOGY AND APPLIED PHARMACOLOGY,      [PMID:41475526] [10.1016/j.taap.2025.117698]
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