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Merck

C121800

L-Cysteine hydrochloride hydrate

99%, for peptide synthesis

Synonym(s):

L-Cysteine·HCl hydrate

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About This Item

Linear Formula:
HSCH2CH(NH2)CO2H·HCl·xH2O
CAS Number:
Molecular Weight:
157.62 (anhydrous basis)
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
EC Number:
200-157-7
MDL number:
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Product Name

L-Cysteine hydrochloride hydrate, 99%

Quality Level

assay

99%

form

solid

optical activity

[α]23/D +5.2°, c = 2 in 5 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

technique(s)

affinity chromatography: suitable

color

white

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

Cl[H].[H]O[H].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 hydrate also known as L-Cysteine·HCl hydrate, is commonly used as a starting material in the synthesis of L-cysteine (alkylated, acidic, and alcoholic) derivatives.

Application

L-Cysteine hydrochloride hydrate is used as a standard solution to determine the quantity of thiol groups attached on mucoadhesiveness.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Mucoadhesive thiolated chitosans as platforms for oral controlled drug delivery: synthesis and in vitro evaluation
M Roldo
European Journal of Pharmaceutics and Biopharmaceutics, 57, 115-121 (2004)
Cysteine based novel noncompetitive inhibitors of urease (s)?Distinctive inhibition susceptibility of microbial and plant ureases
Z Amtul
Bioorganic & Medicinal Chemistry, 14, 6737-6744 (2006)
Ana Odetth Quintana-Escobar et al.
Plants (Basel, Switzerland), 12(24) (2023-12-23)
Plant growth regulators (PGR) are essential for somatic embryogenesis (SE) in different species, and Coffea canephora is no exception. In our study model, previously, we have been able to elucidate the participation of various genes involved in SE by using