![]() L-Cysteine methyl ester hydrochloride structure
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Common Name | L-Cysteine methyl ester hydrochloride | ||
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CAS Number | 18598-63-5 | Molecular Weight | 171.646 | |
Density | N/A | Boiling Point | 197.2ºC at 760 mmHg | |
Molecular Formula | C4H10ClNO2S | Melting Point | 142 °C (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | 73.1ºC | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Use of L-Cysteine methyl ester hydrochlorideMecysteine hydrochloride is an antitussive, and an expectorant agent, used to relieve breathing difficulties caused by mucus. |
Name | methyl (2R)-2-amino-3-sulfanylpropanoate,hydrochloride |
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Synonym | More Synonyms |
Description | Mecysteine hydrochloride is an antitussive, and an expectorant agent, used to relieve breathing difficulties caused by mucus. |
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Related Catalog |
Boiling Point | 197.2ºC at 760 mmHg |
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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) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
![]() GHS07 |
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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 0 | |
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DownStream 9 | |
HS Code | 2930909090 |
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Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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 ... |
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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... |
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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... |
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 |