Skip to Content
Merck
All Photos(1)

Documents

775444

Sigma-Aldrich

Tris(1-pyrrolidinyl)phosphine

97%

Synonym(s):

Tripyrrolidinophosphine, Tris(N-pyrrolidinyl)phosphine, Tris(pyrrolidino)phosphine, Phosphorous acid tripyrrolidide, Tris(N,N-tetramethylene)phosphorous acid triamide

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H24N3P
CAS Number:
Molecular Weight:
241.31
Beilstein:
1343311
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

refractive index

n20/D 1.528
n20/D 1.53 (lit.)

bp

104 °C/0.1 mmHg (lit.)

density

1.041 at 25 °C
1.049 g/mL at 25 °C (lit.)

functional group

phosphine

SMILES string

C1CCN(C1)P(N2CCCC2)N3CCCC3

InChI

1S/C12H24N3P/c1-2-8-13(7-1)16(14-9-3-4-10-14)15-11-5-6-12-15/h1-12H2

InChI key

PXFLCAQHOZXYED-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Monodentate P-donor ligand.

Used as a phosphitylation reagent for oligonucleotide synthesis.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

209.8 °F

Flash Point(C)

98.8 °C


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Tris(N-pyrrolidinyl)phosphine substituted diiron dithiolate related to iron-only hydrogenase active site: Synthesis, characterization and electrochemical properties
Hou, J., et al.
Journal of Organometallic Chemistry, 691, 4633-4640 (2006)
Xianbin Yang et al.
ACS chemical biology, 7(7), 1214-1220 (2012-04-20)
Chemically synthesized small interfering RNAs (siRNAs) have been widely used to identify gene function and hold great potential in providing a new class of therapeutics. Chemical modifications are desired for therapeutic applications to improve siRNA efficacy. Appropriately protected ribonucleoside-3'-yl S-[β-(benzoylmercapto)ethyl]pyrrolidino-thiophosphoramidite

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service