N,N-Dimethylisobutyramide

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Names

[ CAS No. ]:
21678-37-5

[ Name ]:
N,N-Dimethylisobutyramide

[Synonym ]:
N,N,2-trimethylpropionamide
isobutyric acid dimethylamide
N,N-Dimethylisobutyramide
Propanamide,N,N,2-trimethyl
MFCD00075378
N,N-dimethyl-2-methylpropionamide
N,N-dimethyl-2-methylpropanamide

Chemical & Physical Properties

[ Density]:
0.87g/cm3

[ Boiling Point ]:
173.2ºC at 760mmHg

[ Molecular Formula ]:
C6H13NO

[ Molecular Weight ]:
115.17400

[ Flash Point ]:
63.7ºC

[ Exact Mass ]:
115.10000

[ PSA ]:
20.31000

[ LogP ]:
0.73060

[ Vapour Pressure ]:
1.28mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.439(lit.)

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Dimethylamine
  • 2-Methylpropanoyl chloride
  • (2E,6E)-Farnesol
  • N.N.2.-Trimethyl-1-isopropyl-propenylamin
  • 2-buten-1-ol
  • Geraniol
  • Propargyl alcohol
  • Benzyl alcohol
  • Butanol
  • 2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOSE

DownStream

  • BUT-3-ENYLOXY-TERT-BUTYL-DIMETHYL-SILANE
  • 2-Methyl-3-pentanone
  • 3-Heptanone, 2-methyl-
  • 1-[dimethyl(phenyl)silyl]-2-methylpropan-1-one
  • 1-Bromo-3-methyl-2-butanone
  • 1-Propanol,3-(dimethylamino)-2,2-dimethyl-
  • N,N-DIMETHYLPIVALAMIDE
  • Ghosez′s reagent
  • N,N,2-trimethyl-1-trimethylsilyloxyprop-1-en-1-amine
  • Isobutyraldehyde

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

α-Chloro Enamines, Reactive Intermediates for Synthesis: 1-Chloro-N, N, 2-Trimethylpropenylamine. Haveaux B, et al.

Organic Synth. , 26, (1979)

Infrared spectroscopic studies of N, N-disubstituted amides as models for the peptide bond in hydrogen bonded interactions with water molecules. Henson DB and Swenson CA.

J. Phys. Chem. 77(20) , 2401-6, (1973)


More Articles

Related Compounds

  • N,N-dimethyl-N,N-diphenyl-hexa-2,4-diyne-1,6-diamine
  • N,N-Dimethyl-2-{[(2E)-2-(4-nitrophenyl)-3-phenyl-2-propenoyl]oxy} ethanaminium chloride
  • N,N-dimethylbenzenecarboselenoamide
  • N,N,N-Trimethyl-2-propoxy-1-butanaminium chloride
  • N,N-Diethyl-3-(3-(trifluoromethyl)phenyl)-2-propyn-1-amine hydrochlori de
  • N,N-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-amine