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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock α-Lactose monohydrate - PharmPure™, USP , CAS No.5989-81-1
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
alpha-Lactose monohydrate | Respitose | Fenyramidol (VAN) (*hydrochloride*) | Lactose monohydrate | .alpha.-D-Glucopyranose, 4-O-.beta.-D-galactopyranosyl-, monohydrate | Lactose (JP17) | Spherolac 100 | LACTOSE MONOHYDRATE [EP MONOGRAPH] | (2R,3R,4S,5R,6
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Why this grade PharmPure™, USP PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
alpha-Lactose monohydrate | Respitose | Fenyramidol (VAN) (*hydrochloride*) | Lactose monohydrate | .alpha.-D-Glucopyranose, 4-O-.beta.-D-galactopyranosyl-, monohydrate | Lactose (JP17) | Spherolac 100 | LACTOSE MONOHYDRATE [EP MONOGRAPH] | (2R,3R,4S,5R,6
Spécifications et pureté
PharmPure™, USP
Conditions de stockage de stockage
Room temperature
Noms et identifiants Pubchem Sid 508811269 Sourires canoniques C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O.O IUPAC Name (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol;hydrate InChIKey WSVLPVUVIUVCRA-KPKNDVKVSA-N INCHI 1S/C12H22O11.H2O/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17;/h3-20H,1-2H2;1H2/t3-,4-,5+,6+,7-,8-,9-,10-,11+,12+;/m1./s1 Isomères SMILES C([C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@@H]([C@@H]([C@H]2O)O)O)CO)O)O)O)O.O CAS alternatif 14641-93-1 Poids moléculaire 360.31 Reaxy-Rn 38095197 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=38095197&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 Kingdom Organic compounds Superclass Organic oxygen compounds Classe Organooxygen compounds Subclass Carbohydrates and carbohydrate conjugates Intermediate Tree Nodes Glycosyl compounds Direct Parent O-glycosyl compounds Alternative Parents Disaccharides Oxanes Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic heteromonocyclic compounds Substituents O-glycosyl compound - Disaccharide - Oxane - Secondary alcohol - Hemiacetal - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxide - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. External Descriptors Not available 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.
Structure 3D Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Rotation spécifique [α] 54.4° (c=10, H2O, NH3) Point de fusion (°C) 219°C Poids moléculaire 360.310 g/mol XLogP3 Hydrogen Bond Donor Count 9 Hydrogen Bond Acceptor Count 12 Rotatable Bond Count 4 Exact Mass 360.127 Da Monoisotopic Mass 360.127 Da Topological Polar Surface Area 191.000 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 382.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 10 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 2
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