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ChemicalBook >> CAS DataBase List >>L-Cysteine methyl ester hydrochloride

L-Cysteine methyl ester hydrochloride

CAS No.
18598-63-5
Chemical Name:
L-Cysteine methyl ester hydrochloride
Synonyms
H-Cys-Ome;Methyl L-Cysteinate Hydrochloride;(R)-Cysteine Methyl Ester Hydrochloride;MECYSTEINE HYDROCHLORIDE;Methyl cysteinate hydrochloride;L-Cysteine Methyl ester hydrochloride 98%;actiol;l.j.48;zeotin;acdrile
CBNumber:
CB2327369
Molecular Formula:
C4H10ClNO2S
Molecular Weight:
171.65
MDL Number:
MFCD00038985
MOL File:
18598-63-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08
Product description Number Pack Size Price
L-Cysteine methyl ester hydrochloride 98% 410209 5g $56.6
L-Cysteine methyl ester hydrochloride 98% 410209 25g $83.2
L-Cysteine Methyl Ester Hydrochloride >99.0%(T) C0577 5g $17
L-Cysteine Methyl Ester Hydrochloride >99.0%(T) C0577 25g $32
Mecysteine (hydrochloride) ≥95% 34847 10g $36
More product size

L-Cysteine methyl ester hydrochloride Properties

Melting point 142 °C (dec.)(lit.)
alpha -2.25 º (c=5, 1 N HCl)
Density 1.232 (estimate)
refractive index -2.5 ° (C=20, MeOH)
FEMA 4781 | L-CYSTEINE METHYL ESTER HYDROCHLORIDE
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol, Water (Slightly)
form Crystalline Powder
color White
biological source synthetic
optical activity [α]20/D 1.8°, c = 10 in methanol
Water Solubility Soluble in water
Merck 13,5809
JECFA Number 2270
BRN 3685824
Stability Stable. Incompatible with strong oxidizing agents.
Major Application peptide synthesis
InChI 1S/C4H9NO2S.ClH/c1-7-4(6)3(5)2-8;/h3,8H,2,5H2,1H3;1H/t3-;/m0./s1
InChIKey WHOHXJZQBJXAKL-DFWYDOINSA-N
SMILES Cl[H].COC(=O)[C@@H](N)CS
CAS DataBase Reference 18598-63-5(CAS DataBase Reference)
FDA UNII 33RG619160
UNSPSC Code 12352209
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H303-H315-H319-H335
Precautionary statements  P261-P305+P351+P338-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P304+P340-P405-P501a
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  2
RTECS  HA2460000
1-10
HS Code  29309090
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

L-Cysteine methyl ester hydrochloride price More Price(109)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 410209 L-Cysteine methyl ester hydrochloride 98% 18598-63-5 5g $56.6 2026-04-30 Buy
Sigma-Aldrich 410209 L-Cysteine methyl ester hydrochloride 98% 18598-63-5 25g $83.2 2026-04-30 Buy
TCI Chemical C0577 L-Cysteine Methyl Ester Hydrochloride >99.0%(T) 18598-63-5 5g $17 2023-06-20 Buy
TCI Chemical C0577 L-Cysteine Methyl Ester Hydrochloride >99.0%(T) 18598-63-5 25g $32 2022-04-27 Buy
Cayman Chemical 34847 Mecysteine (hydrochloride) ≥95% 18598-63-5 10g $36 2026-04-30 Buy
Product number Packaging Price Buy
410209 5g $56.6 Buy
410209 25g $83.2 Buy
C0577 5g $17 Buy
C0577 25g $32 Buy
34847 10g $36 Buy

L-Cysteine methyl ester hydrochloride Chemical Properties,Uses,Production

Chemical Properties

white crystalline powder

Uses

Mucolytic agent

Uses

A mucolytic. An effective drug for the treatment of liver failure. Shown to effectively inhibit the binding of ethynylestradiol metabolites to protein and nucleic acids.

Uses

L-Cysteine methyl ester hydrochloride is a biochemical shown to inhibit binding of ethynylestradiol metabolites to protein and nucleic acids. It used in the synthesis of peptides, Preparation of thiazolidine-4-carboxylates with carbonyl compounds.

Definition

ChEBI: Mecysteine hydrochloride is an alpha-amino acid ester.

Preparation

L-Cysteine methyl ester hydrochloride is prepared by esterification of L-cysteine hydrochloride monohydrate with methanol in the presence of hydrogen chloride.

reaction suitability

reaction type: solution phase peptide synthesis

Trade name

Acthiol (Joullié, France), Actiol (Lirca, Italy), Visclair (Sinclair, UK), Aslos-C (Nissin, J), Epectan (Seiko, Japan), Moltanine (Tohok.-Tokyo Tanabe, Japan), Radcol (Nippon Universal, Japan), Sekinin (Tokyo Hosei, Japan).

Synthesis

Methanol

67-56-1

L-Cysteine monohydrochloride

52-89-1

L-Cysteine methyl ester hydrochloride

18598-63-5

3 mL of sulfoxide chloride (SOCl2) was slowly added dropwise to 35 mL of methanol under nitrogen protection in an ice bath. Subsequently, the reaction mixture was stirred at room temperature for 1 hour. After that, 1 g of L-cysteine hydrochloride monohydrate (Cys-HCl-H2O) was added to the above solution in batches. The reaction was continued with the mixed solution at room temperature for 3 hours and then heated to reflux for 1 hour. Upon completion of the reaction, the volatile components and solvent were removed by distillation under reduced pressure, and the resulting residue was recrystallized using a solvent mixture of methanol-dichloromethane (CH3OH-CH2Cl2) to give 0.84 g of the white solid product L-cysteine methyl ester hydrochloride in 85.9% yield. The product was analyzed by infrared spectroscopy (IR, KBr press) showing characteristic absorption peaks: 3040.4 cm-1 (strong, NH2 stretching vibration), 1709.7 cm-1 (strong, C=O stretching vibration), 2580 cm-1 (weak, SH stretching vibration). The nuclear magnetic resonance hydrogen spectrum (1H NMR, D2O as solvent, TMS as internal standard) data were as follows: δ 4.453 (t, 1H, CH, J = 5.2 Hz), 3.871 (s, 3H, CH3), 3.164 (t, 2H, CH2, J = 6.4 Hz). Elemental analysis results: Calculated values (C4H10NO2SCCl): C, 27.99%; H, 5.87%; N, 8.16%. Measured values: C, 28.11%; H, 6.01%; N, 8.08%.

References

[1] European Journal of Medicinal Chemistry, 2014, vol. 74, p. 199 - 215
[2] Journal of Organic Chemistry, 2013, vol. 78, # 9, p. 4270 - 4277
[3] Tetrahedron Asymmetry, 2000, vol. 11, # 21, p. 4255 - 4261
[4] Journal of the American Chemical Society, 2008, vol. 130, # 15, p. 5052 - 5053
[5] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 176 - 187,12

67-56-1
52-89-1
18598-63-5
Synthesis of L-Cysteine methyl ester hydrochloride from Methanol and L-Cysteine monohydrochloride
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View Lastest Price from L-Cysteine methyl ester hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
L-Cysteine methyl ester hydrochloride pictures 2026-07-27 L-Cysteine methyl ester hydrochloride
18598-63-5
1KG 98%min 500kgs WUHAN FORTUNA CHEMICAL CO., LTD
H-L-Cys-OMe.HCl pictures 2026-07-27 H-L-Cys-OMe.HCl
18598-63-5
1kg 98% 1T+ Sichuan HongRi Pharma-Tech Co.,Ltd
L-Cysteine methyl ester hydrochloride pictures 2026-07-15 L-Cysteine methyl ester hydrochloride
18598-63-5
$29.00 99.91% 10g TargetMol Chemicals Inc.
L-Cysteine methyl ester hydrochloride(Acdrile) L-Cys-OMe·HCl L-Cysteine methyl ester hydrochloride≥ 98.5% (Titration) methyl cysteine hydrochloride H-CYS-OME HCL H-CYS(ME)OH HYDROCHLORIDE L-CYSTEINE METHYL ESTER HYDROCHLORIDE L-CYSTEINE METHYL ESTER MONOHYDROCHLORIDE L-CYSTEIN METHYL ESTER HYDROCHLORIDE acdrile actiol l.j.48 methylester,hydrochloride,l-cystein pectite visclair zeotin Methyl α-aMino-β-Mercaptopropionate hydrochloride Methyl β-Mercaptoalanine hydrochloride L-Cysteine Methyl ester hydrochloride, 98% 25GR L-Cysteine Methyl ester hydrochloride, 98% 5GR Methyl (R)-2-AMino-3-Mercaptopropanoate Hydrochloride NSC 161611 (R)-Methyl 2-aMino-3-Mercaptopropanoate hydrochloride L-CYSTEINE METHYL ESTER HYDROCHLORIDECRY STALLINE L-CYSTEINE METHYL ESTER HYDROCHLORIDE, 9 8% Mecysteine HCL CYS-OME.HCL L-Cysteine Methyl Ester HCl L-Cystein methyl ester HCl H-CYS(ME)-OH . HCL Cysteine methyl·hydrochloride L-Cyseinemethyl hydrochloride L-Methylcyseine hydrochloride M-Cysten Methyl L-cysteine hydrochloride L(-)-Cysteine Mehtyl Ester Hydrochloride L-Cysteine methyl ester hydrochloride(Cys-Ome·HCl) ,98% L-Cysteine methyl es L-Cysteine methyl ester hydrochloride,0.98 L-Cysteine methyl ester hydrochloride USP/EP/BP -Cysteine methyL (R)-METHYL 2-AMINO-3-MERCAPTOPROPANOATE HCL L-Cysteine Methyl Ester Hydrochloride > methyl (2R)-2-amino-3-sulfanylpropanoate,hydrochloride [(2R)-3-mercapto-1-methoxy-1-oxopropan-2-yl]ammonium H-L-Cys-OMe.HCl L-Cysteine, methyl ester, hydrochloride (9CI) L-Cysteine methyl ester hydrochloride, 10 mM in DMSO L-Cysteine methyl ester hydrochloride (R)-Cysteine Methyl Ester Hydrochloride H-Cys-Ome L-Cysteine Methyl ester hydrochloride 98% MECYSTEINE HYDROCHLORIDE Methyl cysteinate hydrochloride Methyl L-Cysteinate Hydrochloride 18598-63-5 18698-63-5 C4H9NO2SHCl
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