Substance
ID:351077
Names and Identifiers
IUPAC name
(2R)-2-amino-3-sulfanylpropanoic acid
IUPAC Traditional name
L-cysteine
Synonyms
L-半胱氨酸(R)-2-Amino-3-mercaptopropionic acid(R)-2-氨基-3-巯基丙酸L-Cysteine
Registration numbers
CAS Number
PubChem SID
Beilstein Number
EC Number
MDL Number
Properties
Product Information
Impurities
endotoxin, tested
Biological Source
from non-animal source
Suitability
suitable for cell culture
suitable for manufacturing use
Grade
EP
PharmaGrade
USP
Linear Formula
HSCH2CH(NH2)CO2H
Quality Level
GMP-COMPENDIA
Purity
≥98%
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
European Hazard Symbols
Harmful (Xn)GHS Signal Word
Warning
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
German water hazard class
1
GHS Hazard statements
H302
MSDS Link
RTECS
HA1600000
Risk Statements
22
Storage Temperature
20-25°C
Physical Property
Melting Point
220 °C (dec.)(lit.)
Solubility
H2O: soluble25 mg/mL
Molecule Details
Biochem/physiol Actions
NMDA glutamatergic receptor agonist.
Non-animal source L-cysteine is used as a cell culture media component for the commercial biomanufacture of therapeutic recombinant proteins and monoclonal antibodies.
Quality
Manufactured and Packaged under cGMP
NMDA glutamatergic receptor agonist.
Non-animal source L-cysteine is used as a cell culture media component for the commercial biomanufacture of therapeutic recombinant proteins and monoclonal antibodies.
Quality
Manufactured and Packaged under cGMP
Molecular Spectra
No Data Available
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References
No Data Available
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