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131890-26-1

131890-26-1 Structure

131890-26-1 Structure
IdentificationBack Directory
[Name]

Bis[(2-di-i-propylphosphino]ethyl)amine, min. 97%
[CAS]

131890-26-1
[Synonyms]

Bis[(2-di-i-propylphosphino]ethyl)aMine
Bis((2-diisopropylphosphino)ethyl)-amine
Bis[(2-diisopropylphosphino]ethyl)amine solution
Bis[(2-di-i-propylphosphino]ethyl)amine, min. 97%
Bis[2-(diisopropylphosphino)ethyl]aMine, 10% w/w soln. in THF
Bis[(2-di-i-propylphosphino)ethyl]amine(10 wt% in tetrahydrofuran)
Bis[(2-di-i-propylphosphino)ethyl]aMine, Min. 97% (10 wt% in tetrahydrofuran)
[Molecular Formula]

C16H37NP2
[MDL Number]

MFCD17018778
[MOL File]

131890-26-1.mol
[Molecular Weight]

305.419
Chemical PropertiesBack Directory
[Boiling point ]

375.9±27.0 °C(Predicted)
[density ]

0.884 g/mL at 25 °C
[Fp ]

-17 °C
[refractive index ]

1.4180
[form ]

liquid
[pka]

10.42±0.19(Predicted)
[color ]

pale yellow to colorless
[Water Solubility ]

Immiscible with water.
[Sensitive ]

Air Sensitive
[Exposure limits]

ACGIH: TWA 50 ppm; STEL 100 ppm (Skin)
OSHA: TWA 200 ppm(590 mg/m3)
NIOSH: IDLH 2000 ppm; TWA 200 ppm(590 mg/m3); STEL 250 ppm(735 mg/m3)
[InChI]

1S/C16H37NP2/c1-13(2)18(14(3)4)11-9-17-10-12-19(15(5)6)16(7)8/h13-17H,9-12H2,1-8H3
[InChIKey]

FTVIGQGOGIHMBS-UHFFFAOYSA-N
[SMILES]

CC(C)P(CCNCCP(C(C)C)C(C)C)C(C)C
Safety DataBack Directory
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-19-36/37-40
[Safety Statements ]

16-26-36/37
[RIDADR ]

UN 2056 3 / PGII
[WGK Germany ]

3
[HS Code ]

2931.39.0030
[HazardClass ]

3
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Acute Tox. 4 Oral
Carc. 2
Eye Irrit. 2
Flam. Liq. 2
Skin Irrit. 2
STOT SE 3
Questions And AnswerBack Directory
[Reaction]

  1. Ligand for the osmium dehydrogenation of alcohols
  2. Ligand for the ruthenium dehydrogenation of alcohols
  3. Ligand for the iron catalyzed production of hydrogen from methanol
  4. Ligand for the iron catalyzed hydrogenation of esters to alcohols
Reactions of 131890-26-1
Hazard InformationBack Directory
[Uses]

Bis[2-(diisopropylphosphino)ethyl]amine acts as ligand and form complexes with ruthenium, which finds application in the dehydrogenation of ethanol.
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