L-Cysteine methyl ester hydrochloride

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Names

[ CAS No. ]:
18598-63-5

[ Name ]:
L-Cysteine methyl ester hydrochloride

[Synonym ]:
Actiol
H-Cys-OMe·HCl
Mecystein HCl
cysteine methyl ester hydrochloride
methyl L-cysteinate hydrochloride
Acdrile
MFCD00038985
Methyl L-cysteinate hydrochloride (1:1)
EINECS 242-435-0
L-Cysteine, methyl ester, hydrochloride (1:1)
hydrochloride*H-Cys-OMe
Methyl cysteine HCl
H-Cys-OMe.HCl
L-Cysteine Methyl Ester Hydrochloride
L-Cysteinemethylesterhydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
197.2ºC at 760 mmHg

[ Melting Point ]:
142 °C (dec.)(lit.)

[ Molecular Formula ]:
C4H10ClNO2S

[ Molecular Weight ]:
171.646

[ Flash Point ]:
73.1ºC

[ Exact Mass ]:
171.012070

[ PSA ]:
91.12000

[ LogP ]:
0.91880

[ Vapour Pressure ]:
0.384mmHg at 25°C

[ Index of Refraction ]:
-2.5 ° (C=20, MeOH)

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
HA2460000
CHEMICAL NAME :
Cysteine, methyl ester, hydrochloride, L-
CAS REGISTRY NUMBER :
18598-63-5
LAST UPDATED :
199210
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C4-H9-N-O2-S.Cl-H
MOLECULAR WEIGHT :
171.66
WISWESSER LINE NOTATION :
SH1YZVO1 &GH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2300 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
YAKUD5 Gekkan Yakuji. Pharmaceuticals Monthly. (Yakugyo Jihosha, Inaoka Bldg., 2-36 Jinbo-cho, Kanda, Chiyoda-ku, Tokyo 101, Japan) V.1- 1959- Volume(issue)/page/year: 24,2331,1982
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1340 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NIIRDN Drugs in Japan (Ethical Drugs). (Yakugyo Jiho Co., Ltd., Tokyo, Japan) Volume(issue)/page/year: 6,829,1982 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
60 gm/kg/30D-C
TOXIC EFFECTS :
Liver - other changes Kidney, Ureter, Bladder - other changes Blood - normocytic anemia
REFERENCE :
KSRNAM Kiso to Rinsho. Clinical Report. (Yubunsha Co., Ltd., 1-5, Kanda Suda-Cho, Chiyoda-ku, KS Bldg., Tokyo 101, Japan) V.1- 1960- Volume(issue)/page/year: 14,1407,1980

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
2

[ RTECS ]:
HA2460000

[ HS Code ]:
2930909090

Precursor & DownStream

Precursor

DownStream

  • Dimethyl cystinate
  • N-phenylmethoxybenzamide
  • L-Cystine, 1,1'-dimethyl ester, hydrochloride
  • benzoic acid
  • (6R)-6-amino-1,4-thiazepan-5-one
  • N,S-DIACETYL-L-CYSTEINE METHYL ESTER
  • tert-butyl ((4-cyanothiazol-2-yl)Methyl)carbaMate
  • Methyl (4R)-2-oxo-1,3-thiazolidine-4-carboxylate
  • L-Cystine

Customs

[ HS Code ]: 2930909090

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

Articles

Steroidal sapogenins and glycosides from the fibrous roots of Ophiopogon japonicus and Liriope spicata var. prolifera with anti-inflammatory activity.

Chem. Pharm. Bull. 63(3) , 187-94, (2015)

Two new steroidal glycosides (1 and 2), together with 15 known compounds (3-17) were isolated from the fibrous roots of Ophiopogon japonicus, and three new steroidal glycosides (18-20), together with ...

Triterpene glycosides and other polar constituents of shea (Vitellaria paradoxa) kernels and their bioactivities.

Phytochemistry 108 , 157-70, (2014)

The MeOH extract of defatted shea (Vitellaria paradoxa; Sapotaceae) kernels was investigated for its constituents, and fifteen oleanane-type triterpene acids and glycosides, two steroid glucosides, tw...

The role of hydrogen bonding in the selectivity of L-cysteine methyl ester (CYSM) and L-cysteine ethyl ester (CYSE) for chloride ion.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 61(5) , 845-54, (2005)

The interaction of cysteamine (CY), L-cysteine methyl ester (CYSM), and L-cysteine ethyl ester (CYSE) with nitrate, sulfate, perchlorate, dihydrogen phosphate, and chloride ions was investigated using...


More Articles


Related Compounds

  • DL-cysteine methyl ester hydrochloride
  • DL-cysteine methyl ester hydrochloride
  • S-trityl-L-cysteine methyl ester hydrochloride
  • S-Methyl-L-cysteine methyl ester hydrochloride
  • S-Benzyl-L-cysteine methyl ester hydrochloride
  • S-Methyl-L-cysteine methyl ester hydrochloride
  • 4-Cyano-3-(difluoromethyl)-2-hydroxypyridine-5-acetonitrile
  • 2-bromo-6-(difluoromethyl)pyridin-4-amine
  • 2,2-Dimethyl-3-(trifluoroacetamido)propanoic acid
  • 2,2-Dimethyl-3-{[(prop-2-en-1-yloxy)carbonyl]amino}propanoic acid
  • 2,3-Difluoro-4-iodobenzotrifluoride
  • Ethyl 2,2-difluoro-2-(4-fluoro-2-(trifluoromethyl)phenyl)acetate
  • 2-(3-Ethoxypyridin-2-yl)-2,2-difluoroacetic acid
  • Ethyl 2-(5-cyclopropylpyridin-2-yl)-2,2-difluoroacetate
  • 2,2-Difluoro-2-(4-(2-methoxyethoxy)phenyl)acetic acid
  • 2-Amino-3-bromopyridine-4-thiol
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