Cas no 14344-46-8 (N-Methyl-L-cysteine Hydrochloride)

N-Methyl-L-cysteine Hydrochloride structure

14344-46-8 structure

Product Name:N-Methyl-L-cysteine Hydrochloride

CAS No:14344-46-8

MF:C₄H₁₀ClNO₂S

MW:171.6456990242

MDL:MFCD00832046

CID:149993

PubChem ID:2795199

Update Time:2025-04-19

N-Methyl-L-cysteine Hydrochloride Chemical and Physical Properties

Names and Identifiers

- L-Cysteine, N-methyl-,hydrochloride (1:1)
- 3-MERCAPTO-2-(METHYLAMINO)PROPANOIC ACID HYDROCHLORIDE
- 3-Mercapto-2-(methylamino)-propanoic acid hydrochloride
- N-Methyl-L-cysteine Hydrochloride
- (R)-N-methylcysteine hydrochloride
- Cysteine,N-methyl-,hydrochloride,L
- Cysteine,N-methyl-,hydrochloride,L-(8CI)
- HCl*HNMe-Cys-OH
- L-Cysteine,N-methyl-,hydrochloride
- L-Cysteine,N-methyl-,hydrochloride (6CI,9CI)
- L-N-Methylcysteine HCl
- L-N-Methylcysteine hydrochloride
- N-Me-Cys-OH hydrochloride salt
- N-Me-L-Cys-OH*HCl
- Cysteine, N-methyl-, hydrochloride, L-
- L-Cysteine, N-methyl-, hydrochloride
- Cysteine, N-methyl-, hydrochloride, L- (8CI)
- L-Cysteine, N-methyl-, hydrochloride (6CI, 9CI)
- 2-(methylamino)-3-sulfanylpropanoic acid hydrochloride
- 2-(methylamino)-3-sulfanylpropanoic acid, chloride
- SBB053575
- 4317AD
- OR28148
- CHM0010581
- SY237929
- 3-Thio-2-(methylamino)propanoic acid hydrochlo
- A901967
- methylcysteine hydrochloride
- L-Methylcysteine hydrochloride
- 3-MERCAPTO-2-(METHYLAMINO)PROPANOICACIDHYDROCHLORIDE
- AKOS015892801
- 3-Mercapto-2-(Methylamino)propanoic Acid HCl
- 2-(methylamino)-3-sulfanylpropanoic acid;hydrochloride
- J-007815
- MFCD16876405
- 14344-46-8
- 3-Thio-2-(methylamino)propanoic acid hydrochloride
- EN300-216082
- CS-0301359
- MFCD00832046
- FT-0637062
- SCHEMBL100538
- 403804-61-5
- MDL： MFCD00832046
- Inchi： 1S/C4H9NO2S.ClH/c1-5-3(2-8)4(6)7;/h3,5,8H,2H2,1H3,(H,6,7);1H
- InChI Key： SFZVXTJDDOYGIS-UHFFFAOYSA-N
- SMILES： Cl.SCC(C(=O)O)NC

Computed Properties

Exact Mass: 171.01200
Monoisotopic Mass: 171.012
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 4
Heavy Atom Count: 9
Rotatable Bond Count: 3
Complexity: 86.1
Covalently-Bonded Unit Count: 2
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Topological Polar Surface Area: 50.3

Experimental Properties

Boiling Point: 242.8oC at 760 mmHg
Flash Point: 242.8 °C at 760 mmHg
PSA: 88.13000
LogP: 0.78170

N-Methyl-L-cysteine Hydrochloride Customs Data

HS CODE：2930909090
Customs Data：

China Customs Code:
2930909090

Overview:

2930909090. Other organic sulfur compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

Declaration elements:

Product Name, component content, use to

Summary:

2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

N-Methyl-L-cysteine Hydrochloride Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
Fluorochem	066618-1g	3-Mercapto-2-(methylamino)propanoic acid hydrochloride	14344-46-8	97%	1g	￡142.00	2022-03-01
TRC	M294875-250mg	N-Methyl-L-cysteine Hydrochloride	14344-46-8		250mg	$ 213.00	2023-09-07
TRC	M294875-2.5g	N-Methyl-L-cysteine Hydrochloride	14344-46-8		2.5g	$ 1616.00	2023-09-07
eNovation Chemicals LLC	D685225-0.25g	N-Methyl-L-cysteine Hydrochloride	14344-46-8	95%	0.25g	$495	2024-07-20
eNovation Chemicals LLC	D685225-1g	N-Methyl-L-cysteine Hydrochloride	14344-46-8	95%	1g	$935	2024-07-20
SHENG KE LU SI SHENG WU JI SHU	sc-482521-250 mg	N-Methyl-L-cysteine Hydrochloride,	14344-46-8		250MG	￥2,933.00	2023-07-10
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N-Methyl-L-cysteine Hydrochloride Suppliers

Amadis Chemical Company Limited

Gold Member

Audited Supplier

(CAS:14344-46-8)N-Methyl-L-cysteine Hydrochloride

Order Number:A901967

Stock Status:in Stock

Quantity:100mg/1g/5g

Purity:99%

Pricing Information Last Updated:Friday, 30 August 2024 12:10

Price ($):328.0/715.0/1948.0

Email:[email protected]

Product Official Link

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2. Emerging investigator series: heterogeneous reactions of sulfur dioxide on mineral dust nanoparticles: from single component to mixed components?

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Related Categories

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