CAS 28798-28-9|H-Cys(Acm)-OH HCl
Introduction：Basic information about CAS 28798-28-9|H-Cys(Acm)-OH HCl, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | H-Cys(Acm)-OH HCl | ||
|---|---|---|---|
| CAS Number | 28798-28-9 | Molecular Weight | 228.69700 |
| Density | 1.315g/cm3 | Boiling Point | 456.5ºC at 760mmHg |
| Molecular Formula | C6H13ClN2O3S | Melting Point | -165ºC (dec.) |
| MSDS | USA | Flash Point | 229.9ºC |
Names
| Name | (2R)-3-(acetamidomethylsulfanyl)-2-aminopropanoic acid,hydrochloride |
|---|---|
| Synonym | More Synonyms |
H-Cys(Acm)-OH HCl BiologicalActivity
| Description | S-(Acetamidomethyl)-L-cysteine hydrochloride is a cysteine derivative[1]. |
|---|---|
| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References | [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-807. |
Chemical & Physical Properties
| Density | 1.315g/cm3 |
|---|---|
| Boiling Point | 456.5ºC at 760mmHg |
| Melting Point | -165ºC (dec.) |
| Molecular Formula | C6H13ClN2O3S |
| Molecular Weight | 228.69700 |
| Flash Point | 229.9ºC |
| Exact Mass | 228.03400 |
| PSA | 117.72000 |
| LogP | 1.11830 |
| Appearance of Characters | Solid |
| Vapour Pressure | 3.66E-10mmHg at 25°C |
| InChIKey | SZWPOAKLKGUXDD-JEDNCBNOSA-N |
| SMILES | CC(=O)NCSCC(N)C(=O)O.Cl |
| Storage condition | 2-8°C |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Safety Phrases | 22-24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
Articles8
More Articles| Side reaction during the deprotection of (S-acetamidomethyl)cysteine in a peptide with a high serine and threonine content. Int. J. Pept. Protein Res. 41(1) , 85-95, (1993) The acetamidomethyl (Acm) group is a widely used protecting group for the thiol of cysteine during the SPPS process. We prepared the amino terminal loop of the snake alpha-neurotoxin, [Cys3,Cys23, Ser... | |
| Acetamidomethyl. A novel thiol protecting group for cysteine. J. Am. Chem. Soc. 94 , 5456, (1972) | |
| Studies on a growth-inhibitory peptide derived from alpha-fetoprotein and some analogs. J. Pept. Res. 57(1) , 29-38, (2001) A 34-amino acid synthetic peptide was derived from the third domain of human alpha-fetoprotein, and the peptide was shown to inhibit estrogen-stimulated growth. Under certain conditions, however, the ... |
Synonyms
| S-acetamidomethyl cysteine hydrochloride |
| S-acetaminomethyl-L-cysteine hydrochloride |
| H-Cys(Acm).HCl |
| S-Acetamidomethyl-L-cystein-Hydrochlorid |
| H-Cys(Acm)-OH HCl |
| H-Cys(Acm)-OH.HCl |
