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Merck
CN

731366

Diethylphosphine

98%

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About This Item

Empirical Formula (Hill Notation):
C4H11P
CAS Number:
627-49-6
Molecular Weight:
90.10
NACRES:
NA.22
PubChem Substance ID:
329764647
UNSPSC Code:
12352001
MDL number:
MFCD00015169

Key Documents

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InChI

1S/C4H11P/c1-3-5-4-2/h5H,3-4H2,1-2H3

SMILES string

CCPCC

InChI key

VZZJVOCVAZHETD-UHFFFAOYSA-N

assay

98%

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

density

0.782 g/mL at 25 °C

functional group

phosphine

Quality Level

100

Related Categories

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1B

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBL2581
SHBH8853
SHBH5914
SHBG0891V
SHBD3154V

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Amanda Preske et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 17(5), 681-686 (2015-12-15)
The most common method of synthesizing colloidal quantum dots (QDs) relies on an increasing particle size through increasing reaction time. We demonstrate a synthesis where the QD size is programmable through the use of a secondary phosphine sulfide precursor. The

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