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C9768

Sigma-Aldrich

DL-Cystein -hydrochlorid

≥95% (TLC), anhydrous

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About This Item

Lineare Formel:
HSCH2CH(NH2)COOH · HCl
CAS-Nummer:
10318-18-0
Molekulargewicht:
157.62
Beilstein:
4150473
EG-Nummer:
233-698-2
MDL-Nummer:
MFCD00064552
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24893195
NACRES:
NA.26

Qualität

anhydrous

Assay

≥95% (TLC)

Form

powder

Methode(n)

cell culture | mammalian: suitable

Farbe

white

mp (Schmelzpunkt)

109-112 °C

Löslichkeit

H2O: soluble

Anwendung(en)

cell analysis

SMILES String

Cl.NC(CS)C(O)=O

InChI

1S/C3H7NO2S.ClH/c4-2(1-7)3(5)6;/h2,7H,1,4H2,(H,5,6);1H

InChIKey

IFQSXNOEEPCSLW-UHFFFAOYSA-N

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Anwendung

DL-Cysteine hydrochloride is used in cell culture. It is also used in photochemical vascular injury (performed using dl-cysteine hydrochloride along with other components). It may be used in the preparation of DL-4-carboxy-3-formyl-2,2,-dimethylthiazolidine.

Biochem./physiol. Wirkung

DL-Cysteine is a racemic mixture of the proteinogenic amino acids L-cysteine and the non-proteinogenic D-cysteine. DL-Cysteine is used as an organic reagent and in comparative physicochemical analysis of processes such as crystallization.
NMDA glutamatergic receptor agonist that is also an agonist at AMPA glutamatergic receptors at high concentration.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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1. (2R,3S)-[U-14C,3-3H1]- and (2R,3R)-[U-14C,2,3-3H2] Cysteine hydrochlorides have been separately synthesised. The latter compound has been shown to have uniform distributions of tritium between C-2 and C-3. 2. The abvoe cysteines and (2R)-[U-14C,3,3,3',3'-3H4]cystine have been converted to samples of penicillin G
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