Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(C2H5O)3P
CAS Number:
Molecular Weight:
166.16
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-552-5
Beilstein/REAXYS Number:
956578
MDL number:
Quality Level
assay
98%
reaction suitability
reaction type: Reductions
impurities
≤1% triethyl phosphate and diethyl phosphite
refractive index
n20/D 1.413 (lit.)
bp
156 °C (lit.)
density
0.969 g/mL at 25 °C (lit.)
SMILES string
CCOP(OCC)OCC
InChI
1S/C6H15O3P/c1-4-7-10(8-5-2)9-6-3/h4-6H2,1-3H3
InChI key
BDZBKCUKTQZUTL-UHFFFAOYSA-N
Application
Used as a reducing agent; can react with electrophiles to form phosphonates or phosphates; forms a stable complex with copper(I) iodide.
Still not finding the right product?
Explore all of our products under Triethyl phosphite
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Skin Sens. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
监管及禁止进口产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Phosphine Ligand Application Guide
Kyriacos Agapiou et al.
Journal of the American Chemical Society, 126(14), 4528-4529 (2004-04-09)
Exposure of enone substrates 1a-18a, which possess appendant ketone, ester, and nitrile moieties, to Et2Zn in the presence of catalytic Cu(OTf)2/P(OEt)3 provides the cyclized products in good to excellent yields and diastereoselectivities. These results represent the first use of ketones
Stowell, J. K.; Widlanski, T. S. et al.
Tetrahedron Letters, 36, 1825-1825 (1995)
Gabriele Albertin et al.
Dalton transactions (Cambridge, England : 2003), 44(35), 15470-15480 (2015-08-04)
Diazoalkane complexes [Ru(Tp)(N2CAr1Ar2)(PPh3)L]BPh4 ( and ) [Tp = tris(pyrazolyl)borate; L = P(OMe)3, P(OEt)3; Ar1 = Ar2 = Ph; Ar1 = Ph, Ar2 = p-tolyl; Ar1Ar2 = C12H8] were prepared by allowing chloro-compounds RuCl(Tp)(PPh3)L to react with diazoalkane in the presence
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T61204-5ML | 04061837358340 |
| T61204-100ML | 04061837358319 |
| T61204-500ML | 04061837358333 |
| T61204-4L | 04061837358326 |

