n-isobutyryl-d-cysteine

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Names

[ CAS No. ]:
124529-07-3

[ Name ]:
n-isobutyryl-d-cysteine

[Synonym ]:
N-Isobutyryl-D-cysteine
MFCD00155641

Chemical & Physical Properties

[ Density]:
1.199g/cm3

[ Boiling Point ]:
401.6ºC at 760 mmHg

[ Melting Point ]:
97-101ºC(lit.)

[ Molecular Formula ]:
C7H13NO3S

[ Molecular Weight ]:
191.24800

[ Flash Point ]:
196.7ºC

[ Exact Mass ]:
191.06200

[ PSA ]:
105.20000

[ LogP ]:
0.53250

[ Vapour Pressure ]:
1.42E-07mmHg at 25°C

[ Index of Refraction ]:
1.507

[ Storage condition ]:
2-8°C

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Liquid chromatographic determination of D- and L-amino acids by derivatization with o-phthaldialdehyde and N-isobutyryl-L-cysteine. Applications with reference to the analysis of peptidic antibiotics, toxins, drugs and pharmaceutically used amino acids.

J. Chromatogr. A. 711 , 201, (1995)

In order to evaluate and extend the applicability of an analytical method that enables the quantitative and simultaneous high-performance liquid chromatographic determination of D- and L-amino acids (...

Chiral N-isobutyryl-cysteine protected gold nanoparticles: preparation, size selection, and optical activity in the UV-vis and infrared.

J. Am. Chem. Soc. 128(34) , 11079-87, (2006)

We have prepared gold nanoparticles covered with N-isobutyryl-l-cysteine and N-isobutyryl-d-cysteine, respectively. These particles with a mean particle size smaller than 2 nm are highly soluble in wa...

Stereospecific interaction between immune cells and chiral surfaces.

J. Am. Chem. Soc. 129(6) , 1496-7, (2007)


More Articles


Related Compounds

  • D-Alanine, N-(2-methyl-1-oxopropyl)- (9CI)
  • N-Acetyl-D-cysteine
  • N-D-gluconoyl-L-cysteine
  • N-p-nitrobenzyloxycarbonyl-D-cysteine p-nitrobenzyl ester
  • n-acetyl-s-benzyl-d-cysteine
  • N-(tert-butyloxycarbonyl)-S-propyl-D-cysteine methyl ester
  • 7-[(E)-but-2-enyl]-3,4,9-trimethyl-1-(2-piperidin-1-ylethyl)-4,5a-dihydropurino[8,7-c][1,2,4]triazin-5-ium-6,8-dione
  • 6-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]hexanoic acid
  • 1-[(E)-but-2-enyl]-7-[(2-fluorophenyl)methyl]-3,9-dimethyl-5a,9a,10,10a-tetrahydro-4H-purino[8,7-c][1,2,4]triazine-6,8-dione
  • 7-[(3-Chlorophenyl)methyl]-1,3,9-trimethyl-4,5a-dihydropurino[8,7-c][1,2,4]triazin-5-ium-6,8-dione
  • 1,3,9-trimethyl-7-[(E)-3-phenylprop-2-enyl]-4,5a-dihydropurino[8,7-c][1,2,4]triazin-5-ium-6,8-dione
  • 2-[(E)-but-2-enyl]-7-tert-butyl-4-methyl-9aH-purino[8,7-b][1,3]oxazol-9-ium-1,3-dione
  • 9-(4-Fluorophenyl)-1-methyl-3-(2-morpholin-4-ylethyl)-4a,6,7,8-tetrahydropurino[7,8-a]pyrimidin-5-ium-2,4-dione
  • 1-[2-[4-(3-Chlorophenyl)piperazin-1-yl]ethyl]-3,4,7,9-tetramethyl-4,5a-dihydropurino[8,7-c][1,2,4]triazin-5-ium-6,8-dione
  • 1-[(E)-but-2-enyl]-8-(3,5-dimethylpyrazol-1-yl)-3,7-dimethyl-5H-purin-7-ium-2,6-dione
  • 8-(3,5-dimethylpyrazol-1-yl)-3,7-dimethyl-1-[(E)-3-phenylprop-2-enyl]-4,5-dihydropurine-2,6-dione
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