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L-Ascorbic Acid

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    L-<wbr/>Ascorbic Acid
  • L-<wbr/>Ascorbic Acid
Cat No: 14656
Biochemicals - Ox Stress Reagents
Cayman

L-Ascorbic acid is a naturally occurring electron donor and therefore serves as a reducing agent.{18457} It is synthesized from glucose in the liver of most mammalian species, excluding humans, non-human primates, or guinea pigs who must obtain it thr...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one
Correlated keywords:
  • 14536-17-5 30208-61-8 50976-75-5 56172-55-5 56533-05-2 57304-74-2 57606-40-3 88845-26-5 89924-69-6 129940-97-2 154170-90-8 259133-78-3 623158-95-2 882690-91-7 884381-69-5 885512-24-3 1018124-03-2 vitamins C ascorbate electrons donors reducing agents glucose antioxidants reduces ascorbic acids livers mammalian species enzymes collagen hydroxylation carnitine synthesis adenosine triphosphate ATP norepinephrine cancers cardiovascular diseases cataracts cardiology metabolism agents oxidative injury injuries humans primates guinea pigs diet dietary tyrosine amidating peptides adenex allercorb antiscorbic antiscorbutic ascoltin ascorbajen ascorbalox ascorbicap ascorbutina ascorell ascorin ascorteal ascorvit C-L 6/PW c-quin c-vimin cantan cantaxin catavin C Ce-Mi-Lin; Ce-Vi-Sol cebicure cebion cebione cecon cegiolan ceglion ceklin celaskon celin cell C cemagyl cenetone quin vimin Ce Mi Lin Ce Vi Sol CL6/PW cereon cergona cescorbat cetamid cetane cetane-caps caps TC cetebe cetemican cevalin cevarol cevatine cevex cevimin cevital cevitamic acids cevitamin cevitan cevitex cewin chewcee ciamin cinal cipca citrovit colascor concemin davitamon C E 300 E300 E-300 hicee hybrin IDO-C IDOC juvamine kangbingfeng L-(+)-ascorbic L-3-keto-threo-hexuronic lactones L-lyxoascorbic L-xyloascorbic L-threo-ascorbic L-threo-hex-2-enonic ?-lactone laroscorbine lemascorb liqui-cee monovitan C liqui cee monovitan-C NSC218455 NSC-218455 NSC33832 NSC-33832 neo-valdrin P1110 pascorbin neo valdrin P 1110 P-1110 planavit C proscorbin redoxon ribena ronotec 100 rontex 100 rovimix C C-EC scorbu C secorbate suncoat VC 40 tanvimil CEC ronotec-100 rontex-100 rovimix-C scorbu-C VC-40 tanvimil-C testascorbic VC 40 VC 97 vaginorm-C vasc vicelat vicin viforcit viscorin viscorin 100M vitace vitacee vitacimin vitacin vitamin C VC-97 VC40 VC97 viscorin-100M vitamisin vitascorbol vitashure 160 xitix xyloascorbic vitashure-160 vitashure160
Product Overview:
L-Ascorbic acid is a naturally occurring electron donor and therefore serves as a reducing agent.{18457} It is synthesized from glucose in the liver of most mammalian species, excluding humans, non-human primates, or guinea pigs who must obtain it through dietary consumption. In humans, L-Ascorbic acid acts as an electron donor for eight different enzymes, including those related to collagen hydroxylation, carnitine synthesis (which aids in the generation of adenosine triphosphate), norepinephrine synthesis, tyrosine metabolism, and amidating peptides.{18461,18452,18453,18454,18456} L-Ascorbic acid demonstrates antioxidant activity that may be of some benefit for reducing the risk of developing chronic diseases such as cancer, cardiovascular disease, and cataracts.{18457}
Size 50 g
Shipping dry ice
CAS Number 50-81-7
Molecular Formula C6H8O6
SMILES OC1=C(O)[C@]([C@@H](O)CO)([H])OC1=O
Molecular Weight 176,1
Formulation A crystalline solid
Purity ≥95%
Custom Code 2932.99
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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