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778451

L-cystéine hydrochloride monohydrate

Name: <SC>L</SC>-cystéine hydrochloride monohydrate
Brand: ALDRICH

Wacker Chemie AG, 98.5-101.0%

Synonyme(s) :

Cysteine hydrochloride monohydrate, Cysteine monohydrate hydrochloride

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A propos de cet article

Formule linéaire :

HSCH₂CH(NH₂)COOH · HCl · H₂O

Numéro CAS:

7048-04-6

Poids moléculaire :

175.63

UNSPSC Code:

12352209

NACRES:

NA.22

PubChem Substance ID:

329767969

EC Number:

200-157-7

Beilstein/REAXYS Number:

5158059

MDL number:

MFCD00065606

eCl@ss:

32160406

Assay:

98.5-101.0%

Form:

powder or crystals

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Propriétés

Quality Level

200

assay

98.5-101.0%

form

powder or crystals

optical activity

[α]/D 5.7 to 6.8°

reaction suitability

reaction type: solution phase peptide synthesis

manufacturer/tradename

Wacker Chemie AG

impurities

≤0.2% any ninhydrin positive substance each (total ≤1.0%), ≤0.5% ninhydrin positive substances: impurity A, ≤200 ppm ammonium

ign. residue

≤0.1%

loss

8-12% loss on drying

solubility

water: 100 mg/mL at 25 °C

anion traces

sulfate (SO₄^2-): ≤0.030%

cation traces

Fe: ≤10 ppm

suitability

clear, colorless for appearance of solution

application(s)

peptide synthesis

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

Description

General description

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

Application

L-Cysteine hydrochloride monohydrate can be used in the synthesis of protein photo-cross-linkers based on 2-aryl-5-carboxytetrazole , and Zn²⁺-doped non-linear optical crystal by conventional slow evaporation solution technique.

Biochem/physiol Actions

Il s′agit d′un antagoniste des récepteurs glutamatergiques de type NMDA.

Legal Information

FERMOPURE is a registered trademark of Wacker Chemie AG

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Classe de stockage

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

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Genetic encoding of 2-aryl-5-carboxytetrazole-based protein photo-cross-linkers

Tian Y and Lin Q

Chemical Communications (Cambridge, England), 54(35), 4449-4452 (2018)

Synthesis and characterisation of transition metal doped l-cysteine hydrochloride monohydrate single crystal by conventional and unidirectional method and its comparative study

Ramachandra RK, et al.

Materials Research Innovations, 20(7), 538-544 (2016)

Harnessing the potential of LPMO-containing cellulase cocktails poses new demands on processing conditions.

Gerdt Müller et al.

Biotechnology for biofuels, 8, 187-187 (2015-11-27)

The emerging bioeconomy depends on improved methods for processing of lignocellulosic biomass to fuels and chemicals. Saccharification of lignocellulose to fermentable sugars is a key step in this regard where enzymatic catalysis plays an important role and is a major

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Numéro d'article de commerce international

Référence	GTIN
778451-1KG	04061826681008
778451-100G	04061833315057
778451-25KG	04061833367551