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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658588Generated: November 1, 2026

N-Acetyl-L-Cysteine → HCID 22791110, compound

https://huagongshe.com/reaction/1658588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-L-CysteineHCID 12035—
ReactantAmmonium HydroxideHCID 14923—
SolventWaterHCID 962—
ProductHCID 22791110HCID 22791110—

Reaction Steps

N-acetyl-L-cysteine ammonium salt can also be obtained by modification of the above procedure as follows. About 6.5 ml. of concentrated ammonium hydroxide is added slowly to a stirred mixture of N-acetyl-L-cysteine (16.3 g., 0.1 mole) in 100 ml. of water. The pH of the mixture should be 7 at the end of the addition. The solvent is allowed to evaporate and the white residue thus obtained when dried to constant weight at 45°C. in vacuo over phosphorous pentoxide provides a quantitative yield (18 g.,) of analytically pure ammonium N-acetyl-L-cysteinate, M.P. 148°- 150°C. (dec.), [ α ]D25 + 20.3°(c 5,H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03965167
Source datasetuspto-grants-1976_06
ORD IDord-a22fcff2296d42d5b7419136abac50c2
Source noteuspto-grants-1976_06