I-BUT-CYS-OH
Synonym(s):N-(2-Methylpropionyl)-L -cysteine
- CAS NO.:124529-02-8
- Empirical Formula: C7H13NO3S
- Molecular Weight: 191.25
- MDL number: MFCD00155635
- SAFETY DATA SHEET (SDS)
What is I-BUT-CYS-OH?
The Uses of I-BUT-CYS-OH
N-Isobutyryl-L-cysteine may be used as a chiral derivatization agent for the determination of D- and L-amino acids in natural/synthetic bioactive peptides, pharmaceutical formulations and absolute configuration of selenomethionine using chromatography techniques.
What are the applications of Application
N-Isobutyryl-L-cysteine is an agent for chiral derivitization
General Description
N-Isobutyryl-L-cysteine is a chiral derivatizing agent, widely used for the separation of amino acid enantiomers.
Properties of I-BUT-CYS-OH
Melting point: | 97-101 °C |
Boiling point: | 401.6±40.0 °C(Predicted) |
Density | 1.199±0.06 g/cm3(Predicted) |
storage temp. | 2-8°C |
pka | 3.26±0.10(Predicted) |
Safety information for I-BUT-CYS-OH
Computed Descriptors for I-BUT-CYS-OH
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Mefenamic Acid IP/BP/EP/USP Diclofenac Sodium IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
I-BUT-CYS-OH
SA 3443
BUCILLAMINE
N-(3-nitratopivaloyl)cysteine ethyl ester
N-ALPHA-T-BOC-ETHYLMERCAPTO-L-CYSTEINE DICYCLOHEXYLAMMONIUM SALT
BREVININ-1
H-MET-PRO-LYS-LYS-LYS-PRO-THR-PRO-ILE-GLN-LEU-ASN-(CYS)-OH
H-TYR-SER-ALA-ASN-SER-ASN-PRO-ALA-MET-ALA-PRO-ARG-GLU-ARG-LYS-ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS-OH
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