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Merck

30089

Sigma-Aldrich

L-Cystein

BioUltra, ≥98.5% (RT)

Synonym(e):

(R)-2-Amino-3-mercaptopropionsäure

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About This Item

Lineare Formel:
HSCH2CH(NH2)CO2H
CAS-Nummer:
Molekulargewicht:
121.16
Beilstein:
1721408
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352209
eCl@ss:
32160406
PubChem Substanz-ID:
NACRES:
NA.26

Produktlinie

BioUltra

Qualitätsniveau

Assay

≥98.5% (RT)

Form

powder or crystals

Optische Aktivität

[α]20/D +8.0±0.5°, c = 5% in 5 M HCl

Methode(n)

HPLC: suitable

Verunreinigungen

insoluble matter, passes filter test
≤0.5% foreign amino acids

Glührückstand

≤0.05% (as SO4)

Verlust

≤0.05% loss on drying, 20 °C (HV)

Farbe

white

mp (Schmelzpunkt)

240 °C (dec.) (lit.)

Löslichkeit

1 M HCl: 1 M at 20 °C, clear, colorless

Anionenspuren

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤50 mg/kg

Kationenspuren

Al: ≤5 mg/kg
As: ≤0.1 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
NH4+: ≤500 mg/kg
Na: ≤100 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

1 M in 1 M HCl

UV-Absorption

λ: 260 nm Amax: 1.5
λ: 280 nm Amax: 0.2

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

InChIKey

XUJNEKJLAYXESH-REOHCLBHSA-N

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Anwendung

L-Cysteine has been used in quenching of unreacted maleimide during antibody grafting. It has also been used in the preparation of nitrosocysteine stock solution, that has been employed to induce S-nitrosylation to achieve reversible cysteine modification.

Biochem./physiol. Wirkung

Cysteine is one of the functional amino acids that regulates metabolism for growth, reproduction, maintenance and immunity. Cysteine provides the disulfide linkage in proteins. It is directly associated with the transport of sulfur. Taurine, a metabolic product of cysteine acts as an antioxidant and controls the cellular redox state. Cysteine is involved in the formation of hydrogen sulfide that is utilized as a signaling molecule.
NMDA-Glutamat-Rezeptoragonist

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


Analysenzertifikate (COA)

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Artikel

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.

Protokolle

Separation of L-Alanine; Glycine; L-Valine; L-Leucine; L-Isoleucine; L-Proline; L-Methionine; L-Serine; L-Threonine; L-Phenylalanine; L-Aspartic acid; L-4-Hydroxyproline; L-Cysteine; L-Glutamic acid; L-Asparagine; L-Lysine; L-Glutamine; L-Histidine; L-Tyrosine; L-Tryptophan; L-Cystine

Chromatograms

application for HPLC

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