Stachyose - 10mM in DMSO , CAS No.10094-58-3

CAS: 10094-58-3 Cat. No.: S580583 Peso molecular: 666.58 Beilstein Registry Number: 5710670 PubChem CID: 2724335
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
s5102 | AKOS025311600 | Stachyose (tetrahydrate) | HY-113529 | STACHYOSETETRAHYDRATE | CCG-270424 | W-106081 | MS-31281 | C13982 | Stachyose hydrate(1:x) | (2S,3R,4S,5R,6R)-2-[[(2R,3R,4S,5R,6S)-6-[[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(h
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
S580583-1ml
1
83,90US$
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
s5102 | AKOS025311600 | Stachyose (tetrahydrate) | HY-113529 | STACHYOSETETRAHYDRATE | CCG-270424 | W-106081 | MS-31281 | C13982 | Stachyose hydrate(1:x) | (2S, 3R, 4S, 5R, 6R)-2-[[(2R, 3R, 4S, 5R, 6S)-6-[[(2R, 3S, 4S, 5R, 6R)-6-[(2S, 3S, 4S, 5R)-3, 4-dihydroxy-2, 5-bis(h
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasC(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O.O.O.O.O
IUPAC Name(2S,3R,4S,5R,6R)-2-[[(2R,3R,4S,5R,6S)-6-[[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol;tetrahydrate
InChIKeyKUVZQLSUXDNGAW-QPIIYOCQSA-N
INCHI1S/C24H42O21.4H2O/c25-1-6-10(28)14(32)17(35)21(41-6)39-3-8-11(29)15(33)18(36)22(42-8)40-4-9-12(30)16(34)19(37)23(43-9)45-24(5-27)20(38)13(31)7(2-26)44-24;;;;/h6-23,25-38H,1-5H2;4*1H2/t6-,7-,8-,9-,10+,11+,12-,13-,14+,15+,16+,17-,18-,19-,20+,21+,22+,23-,24+;;;;/m1..../s1
Isómeros SMILES C([C@@H]1[C@@H]([C@@H]([C@H]([C@H](O1)OC[C@@H]2[C@@H]([C@@H]([C@H]([C@H](O2)OC[C@@H]3[C@H]([C@@H]([C@H]([C@H](O3)O[C@]4([C@H]([C@@H]([C@H](O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O.O.O.O.O
WGK Alemania 3
PubChem CID 2724335
Peso molecular 666.58
Beilstein 5710670

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
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentOligosaccharides
Alternative Parents O-glycosyl compounds  C-glycosyl compounds  Ketals  Oxanes  Tetrahydrofurans  Secondary alcohols  Polyols  Oxacyclic compounds  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oligosaccharide - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Ketal - Oxane - Tetrahydrofuran - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Alcohol - Primary alcohol - Organic oxide - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Punto de fusión (°C)95-105°C
Peso molecular738.600 g/mol
XLogP3
Hydrogen Bond Donor Count18
Hydrogen Bond Acceptor Count25
Rotatable Bond Count11
Exact Mass738.264 Da
Monoisotopic Mass738.264 Da
Topological Polar Surface Area352.000 Ų
Heavy Atom Count49
Formal Charge0
Complexity933.000
Isotope Atom Count0
Defined Atom Stereocenter Count19
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count5
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Huizhi Li, Shishan Zhang, Yanfang Zhao, Jixiang He, Xiangfeng Chen.  (2023)  Identification of raffinose family oligosaccharides in processed Rehmannia glutinosa Libosch using matrix-assisted laser desorption/ionization mass spectrometry image combined with machine learning.  RAPID COMMUNICATIONS IN MASS SPECTROMETRY,  37  (22): (e9635).  [PMID:37817339] [10.1002/rcm.9635]
2. Zhen Qin, Shaoqing Yang, Liming Zhao, Xin You, Qiaojuan Yan, Zhengqiang Jiang.  (2016)  Catalytic Mechanism of a Novel Glycoside Hydrolase Family 16 “Elongating” β-Transglycosylase *.  JOURNAL OF BIOLOGICAL CHEMISTRY,  292  (5): (1666-1678).  [PMID:27956553] [10.1074/jbc.M116.762419]
3. Pei-Hong Fan, Mei-Tong Zang, Jie Xing.  (2014)  Oligosaccharides composition in eight food legumes species as detected by high-resolution mass spectrometry.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  95  (11): (2228-2236).  [PMID:25270891] [10.1002/jsfa.6940]
4. Wanying Zhao, Yanqin Chen, Jun Tan, Yanru Bai, Fudong Ma.  (2025)  Determination of Saccharides in Cottonseed Processing Waste Liquid and By-Products by High Performance Liquid Chromatography with Evaporative Light Scattering Detection (HPLC-ELSD).  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2025.2451758]
5. Wei Wang, Jiarong Zhu, Yizhou Wang, Liangkun Long, Qunying Lin, Jing Wang, Shaojun Ding.  (2025)  Functional characterization of two GH27 ɑ-galactosidases from Penicillium parvum 4–14 and their differential capabilities upon plant biomass degradation.  CARBOHYDRATE RESEARCH,      [PMID:39965390] [10.1016/j.carres.2025.109428]
6. Zhiwei Sun, Liping Liu, Ruiguo Li, Xiangying Zhao, Jianjun Liu, Jiaxiang Zhang.  (2025)  Improved nutritional composition and flavor of mung bean yogurt through fermentation with Lactiplantibacillus plantarum SF28.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2025.106338]
7. Zhou Ruolin, Ren Zhiqing, Ye Jun, Fan Yawei, Liu Xiaoru, Yang Jianyuan, Deng Ze-Yuan, Li Jing.  (2019)  Fermented Soybean Dregs by Neurospora crassa: a Traditional Prebiotic Food.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,  189  (2): (608-625).  [PMID:31077028] [10.1007/s12010-018-02931-w]
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