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778672

Sigma-Aldrich

L-Cysteine

produced by Wacker Chemie AG, Burghausen, Germany, ≥98.0%

Synonym(s):

(R)-2-Amino-3-mercaptopropionic acid

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About This Item

Linear Formula:
HSCH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
121.16
Beilstein:
1721408
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22

grade

produced by Wacker Chemie AG, Burghausen, Germany

Assay

≥98.0%

form

powder

optical activity

[α]/D 8 to 9.5°

reaction suitability

reaction type: solution phase peptide synthesis

impurities

≤0.5% ninhidrin positive substances (each)
≤10 ppm heavy metals
≤300 ppm ammonium

ign. residue

≤0.1%

loss

≤0.5% loss on drying

mp

240 °C (dec.) (lit.)

anion traces

chloride (Cl-): ≤0.04%
sulfate (SO42-): ≤0.03%

cation traces

Fe: ≤10 ppm

suitability

clear, colorless for appearance of solution

SMILES string

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

InChI

1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1

InChI key

XUJNEKJLAYXESH-REOHCLBHSA-N

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General description

This product is supplied from Wacker FERMOPURE® material, but only sold for R&D use only, not for drug, household or other uses.

Application

L-Cysteine has been used as a standard for the quantification of low-molecular-weight (LMW) thiols extracted from Arabidopsis thaliana tissues by HPLC.

Biochem/physiol Actions

NMDA glutamatergic receptor agonist.

Legal Information

FERMOPURE is a registered trademark of Wacker Chemie AG

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1


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Quantification of Low Molecular Weight Thiols in Arabidopsis.
Miao Z, et al.
Journal of integrative plant biology (2015)
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Proceedings of the National Academy of Sciences of the United States of America, 110(51), E5016-E5024 (2013-12-04)
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Georg K A Hochberg et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(16), E1562-E1570 (2014-04-09)
Mammalian small heat-shock proteins (sHSPs) are molecular chaperones that form polydisperse and dynamic complexes with target proteins, serving as a first line of defense in preventing their aggregation into either amorphous deposits or amyloid fibrils. Their apparently broad target specificity
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Nature, 511(7511), 616-620 (2014-07-22)
Tumour oncogenes include transcription factors that co-opt the general transcriptional machinery to sustain the oncogenic state, but direct pharmacological inhibition of transcription factors has so far proven difficult. However, the transcriptional machinery contains various enzymatic cofactors that can be targeted

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