Ascorbic acid - PharmPure™, USP , CAS No.50-81-7

CAS: 50-81-7 Cat. No.: A103536 Fórmula: C6H8O6 Peso molecular: 176.12 Beilstein Registry Number: 84272 Número EC: 200-066-2
Disponible para pedir
GRADE & PURITY PharmPure™ ? PharmPure™ — Aladdin's line of biopharmaceutical raw and starting materials. Use for pharma manufacturing inputs needing high purity and documentation. USP ? United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance.
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(chloran
Storage
Protected from light,Room temperature,Desiccated
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
100g
A103536-100g
3 Disponible
4 Disponible

31,15€

36,36€
Guardar 5,21 € (14.32%)
500g
A103536-500g
1 Disponible
2 Disponible

102,31€

123,13€
Guardar 20,83 € (16.91%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

PharmPure™, USP PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 4270 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

A calcium channel inhibitor.

Specifications

Sinónimos
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(chloran
Especificaciones y pureza
PharmPure™, USP
Mecanismos bioquímicos y fisiológicos
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
Condiciones de almacenamiento de almacenamiento
Protected from light,Room temperature,Desiccated
Enviado en
Normal
Grado
PharmPure™, USP
Nombres e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508813558
Sonrisas canónicas
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
Isómeros SMILES
C([C@@H]([C@@H]1C(=C(C(=O)O1)O)O)O)O
WGK Alemania
1
RTECS
CI7650000
CAS alternativo
53262-66-1,6730-29-6,50-81-7,134-03-2 (monosodium salt)
Número NSC
UN 1648
Número ONU
3
Términos de entrada 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
Peso molecular
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=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseDihydrofurans
SubclassFuranones
Intermediate Tree Nodes Not available
Direct ParentButenolides
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 FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ADRA2B Tclin Alpha-2B adrenergic receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeFechaArticulo
E2607199Certificate of AnalysisMay 11, 2026 A103536
F2209071Certificate of AnalysisMar 11, 2026 A103536
F2209072Certificate of AnalysisMar 11, 2026 A103536
A2219200Certificate of AnalysisOct 29, 2025 A103536
A2219203Certificate of AnalysisOct 29, 2025 A103536
L2110257Certificate of AnalysisSep 09, 2025 A103536
J2122050Certificate of AnalysisAug 11, 2025 A103536
G2326020Certificate of AnalysisJul 31, 2023 A103536
A2331477Certificate of AnalysisFeb 03, 2023 A103536
I2208276Certificate of AnalysisSep 09, 2022 A103536
I2208278Certificate of AnalysisSep 09, 2022 A103536
Propiedades químicas y físicas
SensibilidadLight sensitive.
Rotación específica [α]21 ° (C=10, H2O)
Punto de fusión (°C)190-192°C
Peso molecular176.120 g/mol
XLogP3-1.600
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass176.032 Da
Monoisotopic Mass176.032 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity232.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Citations of This Product
Calculadoras de soluciones
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