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MilliporeSigma

C6852

L-cystéine hydrochloride monohydrate

98.5-101.0% dry basis, suitable for cell culture, non-animal source, meets EP, USP testing specifications

Synonyme(s) :

L-Cysteine hydrochloride hydrate (1:1:1)

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A propos de cet article

Formule linéaire :
HSCH2CH(NH2)COOH · HCl · H2O
Numéro CAS:
Poids moléculaire :
175.63
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
200-157-7
MDL number:
Beilstein/REAXYS Number:
5158059
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Nom du produit

L-cystéine hydrochloride monohydrate, from non-animal source, suitable for cell culture, meets EP, USP testing specifications

biological source

non-animal source

Quality Level

agency

meets EP testing specifications, meets USP testing specifications

assay

98.5-101.0% dry basis

form

powder or crystals

optical activity

[α]20/D 6.1 to 7.8°, c = 8 in 1 M HCl, [α]25/D 5.7 to 6.8°, c = 8 in HCl (6 N)

technique(s)

cell culture | mammalian: suitable

impurities

endotoxin, tested

color

white

solubility

water: 1 g/10 mL, clear, colorless

cation traces

Fe: ≤10 ppm, NH4+: ≤0.02%

application(s)

pharmaceutical (small molecule)

functional group

(sulfhydryl)

storage temp.

room temp

SMILES string

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

InChI

1S/C3H7NO2S.ClH.H2O/c4-2(1-7)3(5)6;;/h2,7H,1,4H2,(H,5,6);1H;1H2/t2-;;/m0../s1

InChI key

QIJRTFXNRTXDIP-JIZZDEOASA-N

General description

L-Cysteine hydrochloride, commonly referred to as Cysteine HCl, is a vital component in biochemical research due to its versatile roles. Derived from the naturally occurring amino acid L-cysteine, this compound plays a crucial part in redox reactions, protein structure, cell culture, and antioxidant activity. Cysteine HCl functions as a reducing agent and a nucleophile in redox reactions. Additionally, it serves as a precursor to glutathione, a potent cellular antioxidant. Its significance extends to protein structure, where it contributes to the formation of disulfide bonds that stabilize protein structures. Cysteine HCl also supports cell growth and viability in cell culture applications. Its widespread applications encompass diverse areas of biochemical research, including redox biology, protein biochemistry, cell biology, and antioxidant investigations.

Application

L-Cysteine hydrochloride monohydrate has been used as a component of yeast dropout media for culturing yeasts. It has also been used as a component of differential reinforced clostridial broth (DRCM) for the isolation of clostridia.

Biochem/physiol Actions

Il s′agit d′un antagoniste des récepteurs glutamatergiques de type NMDA.
Cysteine (Cys) is a sulfur-containing amino acid that modulates metabolism for growth, reproduction and immunity. It provides the disulfide linkage in proteins and in involved in the transport of sulfur. Cysteine is involved in the formation of hydrogen sulfide that functions as a signaling molecule. Cys residues are present at the catalytic sites of various enzymes.

Features and Benefits

  • Suitable for Cell Culture and Biochemical research
  • High-quality compound suitable for multiple research applications

Other Notes

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Classe de stockage

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Articles

Importance and uses of cysteine in serum-free eukaryotic, including hybridoma and Chinese Hamster Ovary (CHO) cell, cultures

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.


Theresa Mau et al.
mSphere, 4(2) (2019-03-22)
Between October 2016 and June 2017, a C57BL/6J mouse colony that was undergoing a pre- and perinatal methyl donor supplementation diet intervention to study the impact of parental nutrition on offspring susceptibility to disease was found to suffer from an
Protocol for the selection of single-domain antibody
fragments by third generation intracellular
antibody capture
Tomoyuki Tanaka & Terence H Rabbitts
Nature (2009)
Richard S. Lord, J. Alexander Bralley
Laboratory Evaluations for Integrative and Functional Medicine (2008)



Numéro d'article de commerce international

RéférenceGTIN
C6852-1KG04061833511619
C6852-100G04061835543472
C6852-25G04061835521715