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N-Acetyl-L-cysteine ethyl ester powder Raw Materials CAS 59587-09-6
Product Overview:
N-Acetyl-L-cysteine ethyl ester powder is a chemical compound whose chemical structure is an ester bond between acetyl and the amino acid cysteine. N-Acetyl-L-cysteine ethyl ester is an ethyl ester compound of cysteine with both hydrophilic and acetyl groups. White to off-white crystalline solid, N-Acetyl-L-cysteine ethyl ester has antioxidant, anti-inflammatory and detoxification properties. It is also used as a supplement to boost immunity and treat certain diseases.
N-Acetyl-L-cysteine ethyl ester powder Raw Materials CAS 59587-09-6 Attributes
MF:C7H13NO3S
MW:191.25
EINECS:/
Specification:N-Acetyl-L-cysteine ethyl ester powder
Sample:N-Acetyl-L-cysteine ethyl ester powder
Brand:N-Acetyl-L-cysteine ethyl ester powder
Appearance: powder
Storage: Cool Dry Place
Brand: chemical Raw Materials
Shelf Life: 2 Years
Test Method: HPLC
N-Acetyl-L-cysteine ethyl ester powder Raw Materials CAS 59587-09-6 Details
Uses and synthesis of N-Acetyl-L-cysteine ethyl ester powder
N-Acetyl-L-cysteine ethyl ester powder is a chemical compound whose chemical structure is an ester bond between acetyl and the amino acid cysteine. N-Acetyl-L-cysteine ethyl ester is an ethyl ester compound of cysteine with both hydrophilic and acetyl groups. White to off-white crystalline solid, N-Acetyl-L-cysteine ethyl ester has antioxidant, anti-inflammatory and detoxification properties. It is also used as a supplement to boost immunity and treat certain diseases.
Applications/Functions of N-Acetyl-L-cysteine ethyl ester powder
N-Acetyl-L-cysteine ethyl ester powder has antioxidant, anti-inflammatory and detoxification effects. It is also used as a supplement to boost immunity and treat certain diseases.
Physicochemical Property of N-Acetyl-L-cysteine ethyl ester powder
Production methodprocess of N-Acetyl-L-cysteine ethyl ester powder
N-Acetyl-L-cysteine ethyl ester is prepared by reacting ethanol with cysteine and then esterifying to form a ethyl ester compound. The reaction is usually carried out under acidic conditions.
