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N,N'-Diacetylcystine

Base Information Edit
  • Chemical Name:N,N'-Diacetylcystine
  • CAS No.:5545-17-5
  • Molecular Formula:C10H16N2O6S2
  • Molecular Weight:324.379
  • Hs Code.:29225090
  • NSC Number:203782,203780
  • DSSTox Substance ID:DTXSID20970791
  • Nikkaji Number:J2.244.904D
  • Mol file:5545-17-5.mol
N,N'-Diacetylcystine

Synonyms:(Ac-Cys-OH);DiNAC;NSC203780;Cystine, N,N'-diacetyl-, L-;2-acetamido-3-[(2-acetamido-2-carboxyethyl)disulfanyl]propanoic acid;(2R)-2-acetamido-3-[[(2R)-2-acetamido-2-carboxyethyl]disulfanyl]propanoic acid;NSC-203780;NSC203782;L-Cystine,N'-diacetyl-;Cystine, N,N'-diacetyl-;Cystine,N'-diacetyl-, L-;SCHEMBL2140974;DTXSID20970791;N,N'-Bis(1-hydroxyethylidene)cystine;NSC-203782;FT-0629434;EN300-717889;2-acetamido-3-[(2-acetamido-3-hydroxy-3-oxo-propyl)disulfanyl]propanoic acid;3-[(2-CARBOXY-2-ACETAMIDOETHYL)DISULFANYL]-2-ACETAMIDOPROPANOIC ACID;2765062-75-5

Suppliers and Price of N,N'-Diacetylcystine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • N,N’-Diacetyl-L-cystine,90%
  • 25g
  • $ 900.00
  • TRC
  • N,N’-Diacetyl-L-cystine,90%
  • 5g
  • $ 205.00
  • Sigma-Aldrich
  • Acetylcysteine impurity C European Pharmacopoeia (EP) Reference Standard
  • a0152000
  • $ 190.00
  • Crysdot
  • N,N'-Diacetyl-L-Cystine 95+%
  • 5g
  • $ 450.00
  • Crysdot
  • N,N'-Diacetyl-L-Cystine 95+%
  • 1g
  • $ 150.00
  • Chem-Impex
  • (Ac-L-Cys-OH)2(Disulfidebond),≥99.5%(Chiralpurity) ≥99.5%(Chiralpurity)
  • 1G
  • $ 128.13
  • Chem-Impex
  • (Ac-L-Cys-OH)2(Disulfidebond),99.5%(Chiralpurity) 99.5%(Chiralpurity)
  • 250MG
  • $ 67.20
  • Chem-Impex
  • (Ac-L-Cys-OH)2(Disulfidebond),≥99.5%(Chiralpurity) ≥99.5%(Chiralpurity)
  • 5G
  • $ 576.58
  • Cayman Chemical
  • N,N'-Diacetyl-L-cystine ≥90%
  • 5g
  • $ 266.00
  • Cayman Chemical
  • N,N'-Diacetyl-L-cystine ≥90%
  • 10g
  • $ 472.00
Total 29 raw suppliers
Chemical Property of N,N'-Diacetylcystine Edit
Chemical Property:
  • Appearance/Colour:White Powder 
  • Vapor Pressure:2.13E-22mmHg at 25°C 
  • Melting Point:55-72 °C 
  • Refractive Index:1.582 
  • Boiling Point:715.5 °C at 760 mmHg 
  • Flash Point:386.5 °C 
  • PSA:183.40000 
  • Density:1.451 g/cm3 
  • LogP:0.32820 
  • Storage Temp.:-15°C 
  • Solubility.:Methanol (Slightly), Water (Slightly) 
  • XLogP3:-0.4
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:9
  • Exact Mass:324.04497858
  • Heavy Atom Count:20
  • Complexity:354
Purity/Quality:

99%, *data from raw suppliers

N,N’-Diacetyl-L-cystine,90% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)NC(CSSCC(C(=O)O)NC(=O)C)C(=O)O
  • Uses A treatment for dermal imflammations caused by leukotriene production. Contains N-acetyl cysteine. (AC-CYS-OH)2 is a disulfide dimer of N-acetylcysteine with immunomodulatory properties. Its intact disulfide bridge has been shown to be important for its ability to modify contact sensitivity/delayed hypersensitivity reactions in mice. At 3 μM/kg/day, DiNAC also demonstrates anti-atherosclerotic effects, improving endothelial function in Watanabe heritable hyperlipidemic rabbits. N,N’-Diacetyl-L-cystine (DiNAC) is a disulfide dimer of N-acetylcysteine with immunomodulatory properties. Its intact disulfide bridge has been shown to be important for its ability to modify contact sensitivity/delayed hypersensitivity reactions in mice.1,2 At 3 μM/kg/day, DiNAC also demonstrates anti-atherosclerotic effects, improving endothelial function in Watanabe heritable hyperlipidemic rabbits. Acetylcysteine EP Impurity C.
Technology Process of N,N'-Diacetylcystine

There total 31 articles about N,N'-Diacetylcystine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With bis(4-methoxyphenyl)telluride; 5,15,10,20-tetraphenylporphyrin; In dichloromethane; isopropyl alcohol; at 0 ℃; for 0.25h; Irradiation;
DOI:10.1021/jo200496r
Guidance literature:
With formic acid; at 60 ℃; for 3h;
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