Cysteine
C₃H₇NO₂SCite "Cysteine"
Cysteine. (n.d.). In Compound. Retrieved from /compound/cysteine/
"Cysteine." Compound, /compound/cysteine/.
@misc{cysteine, title={Cysteine}, url={/compound/cysteine/}}
IUPAC: (2R)-2-Amino-3-sulfanylpropanoic acid
CAS: 52-90-4
Overview
Cysteine is a sulfur-containing amino acid critical for protein structure through disulfide bonds. It is used in food processing and as a mucolytic agent.
Composition
Elemental Composition
Uses
- • Food processing (dough conditioner)
- • Mucolytic drug (NAC)
- • Cosmetics
- • Antioxidant
Fun Facts
- ✦ Most commercial L-cysteine is extracted from human hair or produced by fermentation
Structure
SMILES
C(C(C(=O)O)N)S
Properties
- Type
- organic
- State
- solid
- Molar Mass
- 121.16 g/mol
- Density
- 1.3000 g/cm³
- Melting Point
- 240.0 °C
- Solubility
- very soluble
Molecular Descriptors
- Exact Mass
- 121.0197
- XLogP
- -2.5
- TPSA
- 64.3 Ų
- H-Bond Donors
- 3
- H-Bond Acceptors
- 4
- Rotatable Bonds
- 2
- Heavy Atoms
- 7
- Complexity
- 75.0
Frequently Asked Questions
What is Cysteine?
Cysteine (C₃H₇NO₂S) is a organic compound with the IUPAC name (2R)-2-Amino-3-sulfanylpropanoic acid.
What is the molecular weight of Cysteine?
Cysteine has a molar mass of 121.16 g/mol.
What state is Cysteine at room temperature?
Cysteine is a solid at room temperature.
Is Cysteine organic or inorganic?
Cysteine is classified as an organic compound.
What elements make up Cysteine?
Cysteine (C₃H₇NO₂S) is composed of Hydrogen (H), Carbon (C), Nitrogen (N), Oxygen (O), Sulfur (S).