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767-10-2

767-10-2 Structure

767-10-2 Structure
IdentificationMore
[Name]

1-Butylpyrrolidine
[CAS]

767-10-2
[Synonyms]

1-BUTYLPYRROLIDINE
N-BUTYL PYRROLIDINE
1-butyl-pyrrolidin
N-butyl-Tetrahydropyrrole
Pyrrolidine, 1-butyl-
[EINECS(EC#)]

212-179-4
[Molecular Formula]

C8H17N
[MDL Number]

MFCD00003184
[Molecular Weight]

127.23
[MOL File]

767-10-2.mol
Chemical PropertiesBack Directory
[Boiling point ]

155-157 °C/754 mmHg (lit.)
[density ]

0.814 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.44(lit.)
[Fp ]

97 °F
[storage temp. ]

Refrigerator, Under inert atmosphere
[solubility ]

Chloroform (Sparingly), Ethyl Acetate (Slightly)
[form ]

Oil
[color ]

Colourless
[LogP]

2.209 (est)
[CAS DataBase Reference]

767-10-2(CAS DataBase Reference)
[NIST Chemistry Reference]

1-Butylpyrrolidine(767-10-2)
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

R10:Flammable.
R24/25:Toxic in contact with skin and if swallowed .
[Safety Statements ]

S16:Keep away from sources of ignition-No smoking .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 2929 6.1/PG 2
[WGK Germany ]

2
[RTECS ]

UX9800000
[HazardClass ]

3.2
[PackingGroup ]

III
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

1-Butylpyrrolidine(767-10-2).msds
Hazard InformationBack Directory
[Uses]

1-Butylpyrrolidine can be used in the composition for alcohol recovery solution.
[Preparation]

The synthesis of 1-butylpyrrolidine and its derivatives (1-butylpyrrolidine with a little of 1-butenylpyrrolidines) was developed via a one-pot method from ammonia and 1,4-butandiol. Here, the product of 1-butylpyrrolidine was emphatically investigated, and the yield was 76% under the optimized conditions. Such a route was realized through successive N-alkylation using aqueous ammonia as the nitrogen source over the CuNiPd/ZSM-5 catalyst, which was prepared by a simple incipient wetness method. In this route, 1,4-butandiol not only participated in the formation of the N-heterocycle, but also acted as an alkylating reagent. This work offers a straightforward, economical route for 1-butylpyrrolidine and its derivatives.
synthesis of 1-butylpyrrolidine and its derivatives
One-pot synthesis of 1-butylpyrrolidine and its derivatives from aqueous ammonia and 1,4-butandiol over CuNiPd/ZSM-5 catalysts
Spectrum DetailBack Directory
[Spectrum Detail]

1-Butylpyrrolidine(767-10-2)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

767-10-2(sigmaaldrich)
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