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α-Lactose monohydrate - Ultra pure,≥99.5% (HPLC), high purity , CAS No.5989-81-1

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Item Number
L102285
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L102285-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$315.90
L102285-100g
100g
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Production requires sourcing of materials. We appreciate your patience and understanding.
$508.90
L102285-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,716.90
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Metabolite (5307)

Basic Description

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
Specifications & Purity Ultra pure, ≥99.5%(HPLC)
Shipped In Normal
Grade Ultra pure

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class 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

Names and Identifiers

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
INCHI 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
InChIKey WSVLPVUVIUVCRA-KPKNDVKVSA-N
Smiles C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O.O
Isomeric 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
Alternate CAS 14641-93-1
Molecular Weight 360.31
Reaxy-Rn 38095197
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=38095197&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Specific Rotation[α] 54.4° (c=10, H2O, NH3)
Melt Point(°C) 219°C
Molecular Weight 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

Citations of This Product

1. Zheng Jiang, Hong Wang, Miao Yu, Cheng Qu, Wei Yue, Qinan Wu.  (2023)  A low-cost efficient online derivatization system for the determination of saccharides by high-performance liquid chromatograph-ultraviolet detector.  JOURNAL OF SEPARATION SCIENCE,  46  (20): (2300384). 
2. Haiqing Wang, Wei Shi, Lei Hou, Chunhui Li, Zhiquan Wang, Lei Yang, Juncheng Cao.  (2023)  Quantitative analysis of aqueous biomolecular mixtures by THz spectroscopy based on high-power LiNbO3 radiation source.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,  287  (122075). 
3. Yuqi Yang, Yiyue Guo, You Xu, Yingying Meng, Xing Zhang, Xuejun Xia, YuLing Liu.  (2020)  Factors affecting the buccal delivery of deformable nanovesicles based on insulin–phospholipid complex: an in vivo investigation.  DRUG DELIVERY,     
4. You Xu, Yiyue Guo, Yuqi Yang, Yingying Meng, Xuejun Xia, Yuling Liu.  (2019)  Stabilization of Deformable Nanovesicles Based on Insulin-Phospholipid Complex by Freeze-Drying.  Pharmaceutics,  11  (10): (539). 
5. Rui Li, Jinhu Wang, Yi He, Faqin Dong, Liang Bian, Bowen Li.  (2019)  Mechanochemical Synthesis of Defective Molybdenum Trioxide, Titanium Dioxide, and Zinc Oxide at Room Temperature.  ACS Sustainable Chemistry & Engineering,  (14): (11985–11989). 
6. Jin-Wen Liu, Tingting Chen, Meiqun Cai, Yingfeng Qin, Mei Li.  (2024)  A Dual-Mode Optical Sensing Strategy for Rapid Detection of D-Penicillamine in Pharmaceutical Formulations.  ANALYTICAL LETTERS,     
7. Changmao Yang, Yue Xiao, Yunjun Yan, Houjin Zhang.  (2024)  A xylenol orange-based pH-sensitive sensor array for identification of bacteria and differentiation of probiotic drinks.  Analytical Methods,     
8. Ping Chen, Hui Zhong, Xiao-rong Li, Tingting Zhang, Xiang Wang, Fang Hu, Yubo Yan, Jiaxing Xu, Meisheng Li.  (2024)  Copper-ion-complexed palygorskite as a novel nanozyme with enhanced peroxidase-like activity for sensitive colorimetric sensing.  APPLIED CLAY SCIENCE,  258  (107507). 
9. Wei Cheng, Huilin Wen, Haixia Shen, Chenwei Fu, Erkuang Miao, Dongbao Li, Xiaoqiang Chen, Chi Hu, Ziyi Yu.  (2024)  Enzyme induced polymer degradation as a pathway to create microbial habitats for biomanufacturing intensification.  CHEMICAL ENGINEERING JOURNAL,  495  (153622). 

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