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Boc-Cys-OH

for chiral derivatization, LiChropur, ≥98.5%

Synonym(s):

Boc-L-cysteine

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About This Item

Empirical Formula (Hill Notation):
C8H15NO4S
CAS Number:
Molecular Weight:
221.27
Beilstein:
2450705
MDL number:
UNSPSC Code:
41116105
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

grade

for chiral derivatization

Quality Level

product line

ChiraSelect

Assay

≥98.5%

form

solid

optical activity

[α]20/D +8.0±1.5°, c = 1% in ethanol

optical purity

enantiomeric ratio: ≥99.5:0.5

quality

LiChropur

technique(s)

HPLC: suitable

SMILES string

CC(C)(C)OC(=O)N[C@@H](CS)C(O)=O

InChI

1S/C8H15NO4S/c1-8(2,3)13-7(12)9-5(4-14)6(10)11/h5,14H,4H2,1-3H3,(H,9,12)(H,10,11)/t5-/m0/s1

InChI key

ATVFTGTXIUDKIZ-YFKPBYRVSA-N

General description

Boc-L-cysteine (Boc-Cys-OH) is a high performance liquid chromatography (HPLC) grade chromatographic solvent.

Application

Boc-L-cysteine (Boc-Cys-OH) can may be used as a chromatographic solvent, in an experimental study done to study the biosynthesis of S-(3-hexan-1-ol)-glutathione (3MH-S-glut) and S-(3-hexan-l-ol)-L-cysteine (3MH-S-cys), which act as flavour precursors in wines, in Vitis vinifera grapes exposed to various environmental stress.

Other Notes

Chiral derivatizing agent used together with OPA for assaying the enantiomeric purity of amino acids

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Legal Information

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Xian Li et al.
Biotechnology letters, 41(1), 69-77 (2018-10-27)
To identify potential target genes involved in L-serine biosynthesis in Methylobacterium sp. MB200 and to evaluate the gnd genetically-engineered strains for L-serine production. Five genes that are not associated with the central metabolic pathway but with L-serine biosynthesis were identified
Hui Dong et al.
Biochemical and biophysical research communications, 503(4), 2319-2325 (2018-07-03)
Alanine racemase is a pyridoxal-5'-phosphate (PLP)-dependent enzyme that reversibly catalyzes the conversion of l-alanine to d-alanine. d-alanine is an essential constituent in many prokaryotic cell structures. Inhibition of alanine racemase is lethal to prokaryotes, creating an attractive target for designing
Environmental stress enhances biosynthesis of flavor precursors, S-3-(hexan-1-ol)-glutathione and S-3-(hexan-1-ol)-L-cysteine, in grapevine through glutathione S-transferase activation.
Kobayashi H
Journal of Experimental Botany, 62 (3), 1325-1336 (2011)
Masumi Katane et al.
Biochimica et biophysica acta. Proteins and proteomics, 1868(8), 140442-140442 (2020-05-08)
d-Aspartate oxidase (DDO) is a flavin adenine dinucleotide (FAD)-containing flavoprotein that stereospecifically acts on acidic d-amino acids (i.e., free d-aspartate and d-glutamate). Mammalian DDO, which exhibits higher activity toward d-aspartate than d-glutamate, is presumed to regulate levels of d-aspartate in
Ryushi Kawakami et al.
Journal of bioscience and bioengineering, 124(1), 23-27 (2017-03-28)
A novel amino acid racemase with broad substrate specificity (BAR) was recently isolated from the hyperthermophilic archaeon Pyrococcus horikoshii OT-3. Characterization of this enzyme has been difficult, however, because the recombinant enzyme is produced mainly as an inclusion body in

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