Triethylenephosphoramide

Base Information

Chemical Name:Triethylenephosphoramide
CAS No.:545-55-1
Molecular Formula:C6H12 N3 O P
Molecular Weight:173.155
Hs Code.:2933990090
European Community (EC) Number:208-892-5
NSC Number:221657,9717
UN Number:2501
UNII:GL19M2KE52
DSSTox Substance ID:DTXSID4052716
Nikkaji Number:J3.294H
Wikidata:Q72499282
ChEMBL ID:CHEMBL670
Mol file:545-55-1.mol

Synonyms:TEPA;Triethylenephosphoramide

Suppliers and Price of Triethylenephosphoramide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Triethylenephosphoramide
10mg
$ 130.00

Medical Isotopes, Inc.
Triethylenephosphoramide
25 mg
$ 640.00

Total 1 raw suppliers

Chemical Property of Triethylenephosphoramide

Chemical Property:

Appearance/Colour:colourless granules
Melting Point:41℃
Boiling Point:299 °C at 760 mmHg
PKA:2.74±0.20(Predicted)
Flash Point:134.6 °C
PSA：35.91000
Density:1.47 g/cm³
LogP:-0.14500
Storage Temp.:-20°C
XLogP3:-0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:173.07179901
Heavy Atom Count:11
Complexity:194
Transport DOT Label:Poison

Purity/Quality:: Triethylenephosphoramide ^*data from reagent suppliers

Safty Information:

Pictogram(s): Highly toxic, strong irritant to skin and tissue.
Hazard Codes:Highly toxic, strong irritant to skin and tissue.

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Pesticides -> Insect Sterilants
Canonical SMILES:C1CN1P(=O)(N2CC2)N3CC3
Uses Used as insect chemosterilant; in dyeing. Antineoplastic. Insect chemosterilant; in dyeing, creaseproofing and flameproofing textiles; stabilizer for polymers; in photographic emulsion hardening.

Technology Process of Triethylenephosphoramide

There total 3 articles about Triethylenephosphoramide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: