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
  • 1-(2-methoxyphenyl)-5-(pyridin-4-yl)-1H-1,2,3-triazole-4-carboxylic acid
  • 4-(4-tert-butylphenyl)-4,7-dihydrofuro[3,4-d]pyrimidine-2,5(1H,3H)-dione
  • 4-[4-(methylsulfanyl)phenyl]-4,7-dihydrofuro[3,4-d]pyrimidine-2,5(1H,3H)-dione
  • 1-phenyl-5-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylic acid
  • 1-(3-chlorophenyl)-5-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylic acid
  • 1-(4-chlorophenyl)-5-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylic acid
  • 1-(4-methoxyphenyl)-5-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylic acid
  • 2-Chloro-4-(3-phenyl-1,2,4-oxadiazol-5-yl)quinoline
  • 1-{3-[3-(3-Methylphenyl)-1,2,4-oxadiazol-5-yl]pyridin-2-yl}piperidine-4-carboxylic acid
  • 2-((1-(3-chlorophenyl)-5-(4-methoxyphenyl)-1H-imidazol-2-yl)thio)-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
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