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460982

Sigma-Aldrich

N,N-Diethylbutylamine

97%

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About This Item

Linear Formula:
CH3(CH2)3N(C2H5)2
CAS Number:
4444-68-2
Molecular Weight:
129.24
MDL number:
MFCD00048759
UNSPSC Code:
12352100
PubChem Substance ID:
24869786
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.414 (lit.)

bp

136.5 °C (lit.)

density

0.748 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCN(CC)CC

InChI

1S/C8H19N/c1-4-7-8-9(5-2)6-3/h4-8H2,1-3H3

InChI key

ORSUTASIQKBEFU-UHFFFAOYSA-N

General description

N,N-Diethylbutylamine is an N,N-diethylalkylamine.[1] It has been reported to induce carotenogenesis in Phycomyces blakesleeanus wild type NRRL 1555 and carA mutants C2, C3 and C152.[2]

Application

N,N-Diethylbutylamine may be used for the regioselective syntheses of of 6-(1,1-dimethylallyl) ortho-flavones.[1][3] It was used in the synthesis of N,N-diethylbutylammonium bis(trifluoromethylsulfonyl)imide.[4]

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
01809PH
10910HQ
20610BI
06715TI

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Regioselective syntheses of 6-(1, 1-dimethylallyl)-and 8-(3, 3-dimethylallyl) chrysins.
Daskiewicz J-B, et al.
Tetrahedron, 58(18), 3589-3595 (2002)
Chemical bioregulation of carotenogenesis in Phycomyces blakesleeanus.
Hsu W-J, et al.
Phytochemistry, 29(8), 2447-2451 (1990)
Rearrangement of 5-O-prenyl flavones: a regioselective access to 6-C-(1,1-dimethylallyl)-and 8-C-(3, 3-dimethylallyl)-flavones.
Daskiewicz J-B, et al.
Tetrahedron Letters, 42(41), 7241-7244 (2001)
Solvent Extraction of Sr2+ and Cs+ Based on Hydrophobic Protic Ionic Liquids
Luo H, et al.
Zeitschrift fur Naturforschung, A, 62(5-6), 281-291 (2007)
Shohei Kakinuma et al.
The journal of physical chemistry. B, 122(22), 6033-6047 (2018-05-11)
In this study, we have investigated the effects of cation structures on the temperature dependence of the intermolecular vibrational dynamics of ionic liquids using femtosecond Raman-induced Kerr effect spectroscopy. The ionic liquids used in this study are bis(trifluoromethylsulfonyl)amide [NTf2]- salts

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