Ochratoxin A-d5

Base Information

Chemical Name:Ochratoxin A-d5
CAS No.:666236-28-8
Molecular Formula:C20H18ClNO6
Molecular Weight:403.81302
Hs Code.:
European Community (EC) Number:688-545-6
Nikkaji Number:J1.986.355G
Mol file:666236-28-8.mol

Synonyms:Ochratoxin A-d5;666236-28-8;HY-N6788S1;CS-0627793

Suppliers and Price of Ochratoxin A-d5

Supply Marketing:

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
OchratoxinA-d5
0.5mg
$ 275.00

Sigma-Aldrich
Ochratoxin A-d5 solution 10μg/mL in acetonitrile, analytical standard
2ml
$ 865.00

American Custom Chemicals Corporation
OCHRATOXIN A-D5 95.00%
10MG
$ 2656.50

American Custom Chemicals Corporation
OCHRATOXIN A-D5 95.00%
1MG
$ 837.38

Total 6 raw suppliers

Chemical Property of Ochratoxin A-d5

Chemical Property:

Melting Point:112-113 °C
Flash Point:2℃
PSA：112.93000
LogP:2.96360
Storage Temp.:?20°C
XLogP3:4.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:408.1136487
Heavy Atom Count:28
Complexity:608

Purity/Quality:

NLT 98% ^*data from raw suppliers

OchratoxinA-d5 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:F,Xn
Statements: 11-20/21/22-36
Safety Statements: 16-26-36/37

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC2=C(C=C(C(=C2C(=O)O1)O)C(=O)NC(CC3=CC=CC=C3)C(=O)O)Cl
Isomeric SMILES:[2H]C1=C(C(=C(C(=C1[2H])[2H])C[C@@H](C(=O)O)NC(=O)C2=CC(=C3C[C@H](OC(=O)C3=C2O)C)Cl)[2H])[2H]
Uses Labelled Ochratoxin A (O148500). Ochratoxins are toxic metabolites from Aspergillus orchraceus.

Technology Process of Ochratoxin A-d5

There total 1 articles about Ochratoxin A-d5 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:

Reference yield: 47.0%