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Tris(2-chloroethyl) Phosphate - >93.0%(GC), high purity , CAS No.115-96-8

    Grade & Purity:
  • ≥93%(GC)
In stock
Item Number
T162660
Grouped product items
SKU Size
Availability
Price Qty
T162660-25g
25g
4
$19.90
T162660-100g
100g
3
$59.90
T162660-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$269.90

Basic Description

Synonyms NCGC00258806-01 | J-003352 | Tris( | MFCD00000967 | Tri-beta-chloroethyl phosphate | TRIS(2-CHLOROETHYL) PHOSPHATE [HSDB] | Tris-(2-chloroethyl)fosfat | AKOS009029110 | Tox21_201254 | Ethanol, 2-chloro-, phosphate (3:1) | Tris(2-chloroethyl) orthophosphat
Specifications & Purity ≥93%(GC)
Shipped In Normal
Product Description

Usually used in dynamic air sampling of airborne organophosphate triesters using a solid-phase microextraction device.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Organic phosphoric acids and derivatives
Subclass Phosphate esters
Intermediate Tree Nodes Alkyl phosphates
Direct Parent Trialkyl phosphates
Alternative Parents Organooxygen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Alkyl chlorides  
Molecular Framework Aliphatic acyclic compounds
Substituents Trialkyl phosphate - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as trialkyl phosphates. These are organic compounds containing a phosphate group that is linked to exactly three alkyl chains.
External Descriptors organochlorine compound - trialkyl phosphate

Associated Targets(Human)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488180746
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180746
IUPAC Name tris(2-chloroethyl) phosphate
INCHI InChI=1S/C6H12Cl3O4P/c7-1-4-11-14(10,12-5-2-8)13-6-3-9/h1-6H2
InChIKey HQUQLFOMPYWACS-UHFFFAOYSA-N
Smiles C(CCl)OP(=O)(OCCCl)OCCCl
Isomeric SMILES C(CCl)OP(=O)(OCCCl)OCCCl
WGK Germany 3
RTECS KK2450000
PubChem CID 8295
UN Number 2810
Packing Group I
Molecular Weight 285.48
Beilstein 1(2)337
Reaxy-Rn 1710938

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

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.

8 results found

Lot Number Certificate Type Date Item
F1917194 Certificate of Analysis Apr 11, 2023 T162660
A2314314 Certificate of Analysis Jan 05, 2023 T162660
A2314315 Certificate of Analysis Jan 05, 2023 T162660
A2314330 Certificate of Analysis Jan 05, 2023 T162660
K2418019 Certificate of Analysis Jan 05, 2023 T162660
A2314331 Certificate of Analysis Jan 05, 2023 T162660
E2522015 Certificate of Analysis Jan 05, 2023 T162660
A2314328 Certificate of Analysis Jan 05, 2023 T162660

Chemical and Physical Properties

Solubility Insoluble in water; Soluble in Alcohol
Refractive Index 1.472
Flash Point(°F) 449.6 °F
Flash Point(°C) 232 °C
Boil Point(°C) 192 °C/10 mmHg
Molecular Weight 285.500 g/mol
XLogP3 1.300
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 9
Exact Mass 283.954 Da
Monoisotopic Mass 283.954 Da
Topological Polar Surface Area 44.800 Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 152.000
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

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