2'-Fucosyllactose - ≥90% , CAS No.41263-94-9

CAS: 41263-94-9 Cat. No.: F407623 Molecular Weight: 488.44 EC Number: 807-054-1 PubChem CID: 170484
AVAILABLE TO ORDER
GRADE & PURITY ≥90%
Synonyms
HY-N9965 | (2R,3R,4R,5R)-4-(((2S,3R,4S,5R,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-2,3,5,6-tetrahydroxyhexanal | Lactose, 2'-o-fucosyl- | 2/'-FUCOSYLLACTOS
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100mg
F407623-100mg
3
$39.90
250mg
F407623-250mg
2
$62.90
1g
F407623-1g
3
$171.90
5g
F407623-5g
2
$571.90
25g
F407623-25g
2
$1,428.90
100g
F407623-100g
2
$2,828.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Application:

2'-Fucosyllactose - Synthetic (cas# 41263-94-9) is a human milk sugar oligosaccharide used in infant nutritian products.


Specifications

Synonyms
HY-N9965 | (2R, 3R, 4R, 5R)-4-(((2S, 3R, 4S, 5R, 6R)-4, 5-Dihydroxy-6-(hydroxymethyl)-3-(((2S, 3S, 4R, 5S, 6S)-3, 4, 5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-2, 3, 5, 6-tetrahydroxyhexanal | Lactose, 2'-o-fucosyl- | 2/'-FUCOSYLLACTOS
Specifications & Purity
≥90%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥90%
Names and Identifiers
Canonical SmilesCC1C(C(C(C(O1)OC2C(C(C(OC2OC(C(CO)O)C(C(C=O)O)O)CO)O)O)O)O)O
IUPAC Name(2R,3R,4R,5R)-4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,3,5,6-tetrahydroxyhexanal
InChIKeyHWHQUWQCBPAQQH-BWRPKUOHSA-N
INCHI1S/C18H32O15/c1-5-9(24)12(27)14(29)17(30-5)33-16-13(28)11(26)8(4-21)31-18(16)32-15(7(23)3-20)10(25)6(22)2-19/h2,5-18,20-29H,3-4H2,1H3/t5-,6-,7+,8+,9+,10+,11-,12+,13-,14-,15+,16+,17-,18-/m0/s1
Isomeric SMILES C[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)O[C@@H]2[C@H]([C@H]([C@H](O[C@H]2O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)CO)O)O)O)O)O
PubChem CID 170484
Molecular Weight 488.44

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
ClassOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentOligosaccharides
Alternative Parents Alkyl glycosides  O-glycosyl compounds  Fatty alcohols  Oxanes  Beta-hydroxy aldehydes  Alpha-hydroxyaldehydes  Secondary alcohols  Polyols  Oxacyclic compounds  Acetals  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oligosaccharide - Fatty acyl glycoside - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Fatty alcohol - Beta-hydroxy aldehyde - Fatty acyl - Oxane - Alpha-hydroxyaldehyde - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Aldehyde - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Primary alcohol - Aliphatic heteromonocyclic compound
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





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

12 results found

Lot NumberCertificate TypeDateItem
H2415043Certificate of AnalysisMay 20, 2026 F407623
G2222272Certificate of AnalysisFeb 04, 2026 F407623
E2528155Certificate of AnalysisJun 07, 2025 F407623
G2222271Certificate of AnalysisMay 21, 2024 F407623
F2325848Certificate of AnalysisMay 10, 2023 F407623
F2325855Certificate of AnalysisMay 10, 2023 F407623
F2325860Certificate of AnalysisMay 10, 2023 F407623
F2325862Certificate of AnalysisMay 10, 2023 F407623
F2325876Certificate of AnalysisMay 10, 2023 F407623
L2426194Certificate of AnalysisMay 10, 2023 F407623
L2515014Certificate of AnalysisMay 10, 2023 F407623
G2222270Certificate of AnalysisJun 15, 2022 F407623

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Chemical and Physical Properties
SolubilityDMSO (Slightly), Methanol (Slightly), Water (Slightly)
SensitivityEasy to absorb moisture
Melt Point(°C)>203°C
Molecular Weight488.400 g/mol
XLogP3-6.100
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count15
Rotatable Bond Count10
Exact Mass488.174 Da
Monoisotopic Mass488.174 Da
Topological Polar Surface Area256.000 Ų
Heavy Atom Count33
Formal Charge0
Complexity609.000
Isotope Atom Count0
Defined Atom Stereocenter Count14
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Qinqin Zhao, Liwei Gao, Nuo Xu, Xiuting Zhang, Yuqi Qin, Yinbo Qu, Guodong Liu.  (2025)  An l-fucose-responsive transcription factor cross-regulates the expression of a diverse array of carbohydrate-active enzymes in Trichoderma reesei.  PLoS Genetics,  21  (8): (e1011815).  [PMID:40788923] [10.1371/journal.pgen.1011815]
Solution Calculators
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