nicotinamide adenine dinucleotide
adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1-beta-D-ribofuranosylpyridinium hydroxide, inner salt

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  53-84-9 Dihydronicotinamide Adenine Dinucleotide >98%
  NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage.

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  GV0860 beta-Nicotinamide adenine dinucleotide

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  D0919 b-Nicotinamide Adenine Dinucleotide Hydrate, oxidized form [for Biochemical Research] >95.0%(HPLC)
  SDS

CAS Number: 53-84-9 3D/inchi Other(deleted CASRN): 1083039-67-1 FDA UNII: 0U46U6E8UK Beilstein Number: 3584133 MDL: MFCD00036253 XlogP3-AA: -6.00 (est) Molecular Weight: 663.43151400 Formula: C21 H27 N7 O14 P2 NMR Predictor: Predict (works with chrome, Edge or firefox) Category:cosmetic ingredient for skin conditioning   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search   Physical Properties: Assay: 95.00 to 100.00 Food Chemicals Codex Listed: No Soluble in:   water, 4124 mg/L @ 25 °C (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: CosIng: cosmetic data Cosmetic Uses: skin conditioning   Suppliers: BOC Sciences For experimental / research use only. Dihydronicotinamide Adenine Dinucleotide >98% Odor: characteristic Use: NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. Glentham Life Sciences beta-Nicotinamide adenine dinucleotide Santa Cruz Biotechnology For experimental / research use only. NAD+, Free Acid Sigma-Aldrich For experimental / research use only. b-Nicotinamide adenine dinucleotide hydrate ≥99% TCI AMERICA For experimental / research use only. b-Nicotinamide Adenine Dinucleotide Hydrate, oxidized form [for Biochemical Research] >95.0%(HPLC) sds   Safety Information: Preferred SDS: View   Hazards identification   Classification of the substance or mixture GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. GHS Label elements, including precautionary statements   Pictogram   Hazard statement(s) None found. Precautionary statement(s) None found. Oral/Parenteral Toxicity: Not determined Dermal Toxicity: Not determined Inhalation Toxicity: Not determined   Safety in Use Information: Category: cosmetic ingredient for skin conditioning Recommendation for nicotinamide adenine dinucleotide usage levels up to:   not for fragrance use.   Recommendation for nicotinamide adenine dinucleotide flavor usage levels up to:   not for flavor use.   Safety References: EPI System: View ClinicalTrials.gov:search Daily Med:search AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search EPA Substance Registry Services (TSCA):53-84-9 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :5892 National Institute of Allergy and Infectious Diseases:Data WGK Germany:3 [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate Chemidplus:0000053849 RTECS:UU3450000 for cas# 53-84-9   References:   [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate NIST Chemistry WebBook: Search Inchi Canada Domestic Sub. List: 53-84-9 Pubchem (cid): 5892 Pubchem (sid): 134971502   Other Information: (IUPAC): Atomic Weights of the Elements 2011 (pdf) Videos: The Periodic Table of Videos tgsc: Atomic Weights use for this web site (IUPAC): Periodic Table of the Elements CHEBI: View CHEMBL: View Golm Metabolome Database: Search KEGG (GenomeNet): C00003 HMDB (The Human Metabolome Database): HMDB00902 FooDB: FDB022309 YMDB (Yeast Metabolome Database): YMDB00110 Export Tariff Code: 2933.39.9100 ChemSpider: View Wikipedia: View EFSA Update of results on the monitoring of furan levels in food: Read Report EFSA Previous report: Results on the monitoring of furan levels in food: Read Report EFSA Report of the CONTAM Panel on provisional findings on furan in food: Read Report   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   not found in nature   Synonyms:   adenosine 5'-(trihydrogen diphosphate), 5'->5'-ester with 3-(aminocarbonyl)-1-beta-D-ribofuranosylpyridinium hydroxide, inner salt [[(2R,3S,4R,5R)-5-(6- aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate beta- diphosphopyridine nucleotide   nadide   Articles:   None found yet. Try the PubMed Search.

Notes: NAD (or Nicotinamide adenine dinucleotide) is used extensively in glycolysis and the citric acid cycle of cellular respiration. The reducing potential stored in NADH can be converted to ATP through the electron transport chain or used for anabolic metabolism. ATP "energy" is necessary for an organism to live. Green plants obtain ATP through photosynthesis, while other organisms obtain it by cellular respiration. (wikipedia). Nicotinamide adenine dinucleotide is a A coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. It is found widely in nature and is involved in numerous enzymatic reactions in which it serves as an electron carrier by being alternately oxidized (NAD+) and reduced (NADH). (Dorland, 27th ed) [HMDB]