THIONICOTINAMIDE ADENINE DINUCLEOTIDE CAS#: 4090-29-3; ChemWhat Code: 623152

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameTHIONICOTINAMIDE ADENINE DINUCLEOTIDE
IUPAC NameThio-NAD
Molecular StructureStructure of Thio-NAD CAS 4090-29-3
CAS Registry Number 4090-29-3
EINECS Number207-322-2
MDL NumberMFCD00079609
Beilstein Registry NumberNo data available
Synonymsthio-nicotinamide adenine dinucleotide, thio-NAD+, diphosphoric acid-1-adenosin-5′-ylester-2-[(1R)-1-(3-thiocarbamoyl-pyridinio)-D-1,4-anhydro-ribitol-5-ylester]-betaine, Diphosphorsaeure-1-adenosin-5′-ylester-2-[(1R)-1-(3-thiocarbamoyl-pyridinio)-D-1,4-anhydro-ribit-5-ylester]-betain, adenosine 5′-(trihydrogen diphosphate), 5′->5′-ester with 3-(aminothioxomethyl)-1-β-D-ribofuranosylpyridinium-ate
Molecular FormulaC21H27N7O13SP2 
Molecular Weight679.49
InChIInChI=1S/C21H27N7O13P2S/c22-17-12-19(25-7-24-17)28(8-26-12)21-14(31)13(30)11(39-21)6-37-42(33,34)41-43(35,36)40-16-10(5-29)38-20(15(16)32)27-3-1-2-9(4-27)18(23)44/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,44)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChI KeyDQRRIGAXTAXHLR-NNYOXOHSSA-N
Canonical SMILESc1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)OP(=O)([O-])OP(=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)C(=S)N
Patent Information
No data available

Physical Data

AppearanceLight yellow or yellow-green powder
Description (Association (MCS))Temperature (Association (MCS)), °CPartner (Association (MCS))
Association with compound37apo enzyme S-adenosylhomocysteine hydrolase from human source
Association with compound37apo enzyme S-adenosylhomocysteine hydrolase from Trypanosoma cruzi

Spectra

Description (UV/VIS Spectroscopy)Solvent (UV/VIS Spectroscopy)Absorption Maxima (UV/VIS), nm
Absorption maximaH2O260
Absorption maximaaq. HCl260
Absorption maximaaq. NaOH260

Route of Synthesis (ROS)

Route of Synthesis (ROS) of THIONICOTINAMIDE ADENINE DINUCLEOTIDE CAS 4090-29-3
Route of Synthesis (ROS) of THIONICOTINAMIDE ADENINE DINUCLEOTIDE CAS 4090-29-3
ConditionsYield
With ethylenediaminetetraacetic acid; ethanol; alcohol dehydrogenase at 25℃; for 0.5h; pH=8.4; phosphate buffer; Enzymatic reaction;

Safety and Hazards

GHS Hazard StatementsNot Classified
For more detailed information, please visit ECHA C&L website
Source: European Chemicals Agency (ECHA)
License Note: Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: “Source: European Chemicals Agency, http://echa.europa.eu/”. Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page.
License URL: https://echa.europa.eu/web/guest/legal-notice
Record Name: (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate
URL: https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/213446
Description: The information provided here is aggregated from the “Notified classification and labelling” from ECHA’s C&L Inventory. Read more: https://echa.europa.eu/information-on-chemicals/cl-inventory-database

Other Data

TransportationNONH for all modes of transport
Under the room temperature and away from light
HS Code290621
StorageStore at -20 ℃, sealed and protected from light.
Shelf LifeOne and a half years.
Market PriceUSD
Use Pattern
THIONICOTINAMIDE ADENINE DINUCLEOTIDE CAS#: 4090-29-3 used in conjunction with 3α-hydroxysteroid dehydrogenase (3α-HSD).
THIONICOTINAMIDE ADENINE DINUCLEOTIDE CAS#: 4090-29-3 uesd for the development and mass preparation of total bile acid (TBA) reagents.

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