Ascorbic acid - analytical standard, Moligand™ , CAS No.50-81-7

CAS: 50-81-7 Cat. No.: A103537 Formule: C₆H₈O₆ Poids moléculaire: 176.12 Beilstein Registry Number: 84272 Numéro CE: 200-066-2

QUALITÉ & PURETÉ Analytical standard, Moligand™

Synonyms

Ascorbicap|C-Long|Ferrous ascorbate|phosphorus oxichloride|Ceglion|Cenetone|Cetemican|hexamethyl-disiloxane|Ascorb|Cemagyl|Cipca|Planavit C|Secorbate|Vitacee|Ascorbicab|Scorbacid|Cecon|C-Span|Duoscorb|pentakis(chloranyl)-$l^{5}-phosphane|vitamin C|CE-VI-Sol|Viforcit|Vitacimin|Ascorvit|Ce-Mi-Lin|Cetane-Caps TD|Cevitamin|Kyselina askorbova|Roscorbic|Cereon|Proscorbin|3-Oxo-L-gulofuranolactone|Cegiolan|Cescorbat|l-ascorbic acid|Redoxon|Acidum ascorbicum|Concemin|Vitamisin|Ascorteal|Cee-Caps TD|Natrascorb|Acidum ascorbinicum|Cantan|2-amino-butane|Ribena|Stuartinic|Adenex|Vitacin|Celaskon|Ciamin|Vitace|Dora-C-500|Laroscorbine|ALUMINUM POTASSIUM SULFATE [FCC]|Cee-Vite|L-Xyloascorbic acid|Cevalin|Cevi-Bid|Citriscorb|Acido ascorbico|Allercorb|Ce lent|Cemill|Lemascorb|Meri-C|Cevitex|L-ascorbate|Catavin C|Ferancee|Vicelat|Ascoltin|ascorbic acid|Celin|Cetamid|Cetane-Caps TC|Liqui-Cee|L-Lyxoascorbic acid|3-Keto-L-gulofuranolactone|Cevex|Ascorbajen|Ascorbutina|Cergona|Cevimin|Vicomin C|Ascor-B.I.D.|Cebione|Davitamon C|Xitix|Cebicure|Testascorbic|IDO-C|C-Vimin|Natrascorb injectable|Tolfrinic|Viscorin|Colascor|Cortalex|Acide ascorbique|Arco-cee|Cebion|L-(+)-Ascorbic Acid|L(+)-Ascorbic acid|Scorbu-C|Hybrin|USEPA/OPP Pesticide Code: 020503|Ascorin|Cevital|Cewin|C-Quin|L-Threoascorbic acid|Cantaxin|Cevatine|HYDRAZINE, SULPHATE (1:1)|Antiscorbic vitamin|Cebid|Cevitamic acid

Storage

Protected from light,Room temperature,Desiccated

Shipped In

Normal

Vue d’ensemble

A calcium channel inhibitor.

Spécifications

Synonymes

Ascorbicap | C-Long | Ferrous ascorbate | phosphorus oxichloride | Ceglion | Cenetone | Cetemican | hexamethyl-disiloxane | Ascorb | Cemagyl | Cipca | Planavit C | Secorbate | Vitacee | Ascorbicab | Scorbacid | Cecon | C-Span | Duoscorb | pentakis(chloranyl)-$l^{5}-phosphane | vitamin C | CE-VI-Sol | Viforcit | Vitacimin | Ascorvit | Ce-M Afficher plus

Spécifications et pureté

analytical standard, Moligand™

Mécanismes biochimiques et physiologiques

It protects cells against the damaging effects of radiation and oxygen radicals,increases the rate of mineralization in osteoblasts,reduces Na+/Ca2+ exchange in cultured astrocytes,modulates cyclic nucleotide levels in B and T cells inhibits apoptosis in

Conditions de stockage de stockage

Protected from light,Room temperature,Desiccated

Expédié en

Normal

Grade

Analytical standard, Moligand™

Noms et identifiants

Pubchem Sid

508813562

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813562

Sourires canoniques

OC([C@]([C@@H](O)CO)([H])O1)=C(O)C1=O

IUPAC Name

(2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one

InChIKey

CIWBSHSKHKDKBQ-JLAZNSOCSA-N

INCHI

1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,5+/m0/s1

Isomères SMILES

C([C@@H]([C@@H]1C(=C(C(=O)O1)O)O)O)O

WGK Allemagne

1

RTECS

CI7650000

CAS alternatif

53262-66-1,6730-29-6,50-81-7,134-03-2 (monosodium salt)

Numéro NSC

UN 1648

Numéro ONU

3

Termes d'entrée MeSH

Acid, Ascorbic;Acid, L-Ascorbic;Ascorbate, Ferrous;Ascorbate, Magnesium;Ascorbate, Sodium;Ascorbic Acid;Ascorbic Acid, Monosodium Salt;di-L-Ascorbate, Magnesium;Ferrous Ascorbate;Hybrin;L Ascorbic Acid;L-Ascorbic Acid;Magnesium Ascorbate;Magnesium Ascorbi

Poids moléculaire

176.12

Beilstein

84272

Reaxy-Rn

84272

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=84272&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Dihydrofurans
      • Subclass Furanones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Dihydrofurans
• Subclass: Furanones
• Intermediate Tree Nodes: Not available
• Direct Parent: Butenolides
• Alternative Parents: Vinylogous acids Enoate esters Secondary alcohols Lactones Enediols 1,2-diols Oxacyclic compounds Monocarboxylic acids and derivatives Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 2-furanone - Vinylogous acid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - 1,2-diol - Carboxylic acid ester - Enediol - Secondary alcohol - Lactone - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Primary alcohol - Organooxygen compound - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.
• External Descriptors: Water-soluble vitamins

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Light sensitive.
• Rotation spécifique [α]: 21 ° (C=10, H2O)
• Point de fusion (°C): 190-192°C
• Poids moléculaire: 176.120 g/mol
• XLogP3: -1.600
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 176.032 Da
• Monoisotopic Mass: 176.032 Da
• Topological Polar Surface Area: 107.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 232.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1