Stachyose tetrahydrate - ≥98% , CAS No.10094-58-3

CAS: 10094-58-3 Cat. No.: S1421262 Peso molecular: 666.58 Beilstein Registry Number: 5710670 PubChem CID: 2724335
Disponible para pedir
GRADE & PURITY ≥98%
Storage
Store at 2-8°C,Protected from light,Desiccated
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
S1421262-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
34,90US$
10mg
S1421262-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
53,90US$
25mg
S1421262-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
74,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Desiccated Ships Wet ice 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.

Descripción general

Stachyose tetrahydrate, a functional oligosaccharide, acts as a prebiotic. Stachyose tetrahydrate can prevent indirectly colon cancer cell growth by promoting the proliferation of probiotics or producing beneficial materials in the intestine.

Specifications

Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Desiccated
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
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
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. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
Calculadoras de soluciones
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