thymidine
2(1H)-pyrimidinone, 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-hydroxy-5-methyl-

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  T0233 Thymidine >98.0%(HPLC)(T)
  SDS

Name: 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione CAS Number: 50-89-5 3D/inchi Other(deleted CASRN): 35902-13-7 ECHA EINECS - REACH Pre-Reg: 200-070-4 FDA UNII: VC2W18DGKR Nikkaji Web: J4.548I Beilstein Number: 89285 MDL: MFCD00006537 XlogP3: -1.20 (est) Molecular Weight: 242.23158000 Formula: C10 H14 N2 O5 BioActivity Summary: listing NMR Predictor: Predict (works with chrome, Edge or firefox) Category:cosmetic agents   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 Melting Point: 186.50 °C. @ 760.00 mm Hg Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (est) logP (o/w): -0.930 Soluble in:   water, 7962 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: Alfa Biotechnology For experimental / research use only. Thymidine 98% BOC Sciences For experimental / research use only. Thymidine ≥98% by HPLC Changzhou Longo Chemical Thymidine Coompo For experimental / research use only. Thymidine from Plants ≥96% Dow Chemical Thymidine George Uhe Company Thymidine Glentham Life Sciences Thymidine Santa Cruz Biotechnology For experimental / research use only. Thymidine >98% Sigma-Aldrich: Sigma For experimental / research use only. Thymidine ≥99% sds TCI AMERICA For experimental / research use only. Thymidine >98.0%(HPLC)(T) 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: intraperitoneal-mouse LD50 2512 mg/kg BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) Journal of Pharmacology and Experimental Therapeutics. Vol. 207, Pg. 504, 1978. Dermal Toxicity: Not determined Inhalation Toxicity: Not determined   Safety in Use Information: Category: cosmetic agents Recommendation for thymidine usage levels up to:   not for fragrance use.   Recommendation for thymidine flavor usage levels up to:   not for flavor use.   Safety References: EPI System: View ClinicalTrials.gov:search Daily Med:search Chemical Carcinogenesis Research Information System:Search AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search EPA GENetic TOXicology:Search EPA Substance Registry Services (TSCA):50-89-5 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :5789 National Institute of Allergy and Infectious Diseases:Data WGK Germany:1 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione Chemidplus:0000050884 RTECS:XP2071000 for cas# 50-89-5   References:   1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione NIST Chemistry WebBook: Search Inchi Canada Domestic Sub. List: 50-89-5 Pubchem (cid): 5789 Pubchem (sid): 135060607   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 Metabolomics Database: Search KEGG (GenomeNet): C00214 HMDB (The Human Metabolome Database): HMDB00273 FooDB: FDB012757 YMDB (Yeast Metabolome Database): YMDB00507 Export Tariff Code: 2934.99.9000 MedlinePlusSupp: View VCF-Online: VCF Volatile Compounds in Food 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   bean green bean seedling Search Trop Picture   Synonyms: 1-(2- deoxy-b-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione 1-(2- deoxy-b-D-ribofuranosyl)-5-methyluracil 1-[(4S,2R,5R)-4- hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-1,3-dihydropyrimidine-2,4-dione 1-[(2R,4S,5R)-4- hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-pyrimidine-2,4-dione 1-[(2R,4S,5R)-4- hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione 1-[(2R,4S,5R)-4- hydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-5-methyl-2,4(1H,3H)-pyrimidinedione 1-((2R,4S,5R)-4- hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 5- methyl-2'-deoxyuridine 5- methyldeoxyuridine 5- methyldeoxyurindine 2(1H)- pyrimidinone, 1-(2-deoxy-β-D-erythro-pentofuranosyl)-4-hydroxy-5-methyl-   telbivudine 2'- thymidine L- thymidine   thymine-1 2-deoxy-b-D-ribofuranoside   Articles:   None found yet. Try the PubMed Search.

Notes: Isol. from seedlings of Phaseolus vulgaris (kidney bean) Deoxythymidine is non-toxic and as part of one of the four nucleotides in DNA it is a naturally occurring compound that exists in all living organisms and DNA viruses. RNA has uridine (uracil joined to ribose) instead. Uracil is chemically very similar to thymine, the latter being 5-methyluracil. Since thymine nucleotides are precursors of DNA, not RNA, the prefix "deoxy" is often left out, i.e., deoxythymidine is often just called thymidine.; In its composition, deoxythymidine is a nucleoside composed of deoxyribose (a pentose sugar) joined to the pyrimidine base thymine.; Iododeoxyuridine is a radiosensitizer and increases the amount of DNA damage received from ionizing radiation.; Thymidine (more precisely called deoxythymidine; can also be labelled deoxyribosylthymine, and thymine deoxyriboside) is a chemical compound, more precisely a pyrimidine deoxynucleoside. Deoxythymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. In cell biology it is used to synchronize the cells in S phase.; Thymidine is non-toxic and is a naturally occurring compound that exists in all living organisms and DNA viruses. 25% of DNA is composed of thymidine. RNA does not have thymidine and has uridine instead. Thymidine is a chemical compound which is a pyrimidine nucleoside. Thymidine is the DNA base T, which pairs with adenosine in double stranded DNA.