1,1,1,1-Kestohexaose - ≥98% , CAS No.62512-19-0

CAS: 62512-19-0 Cat. No.: K412899 Molecular Weight: 990.86 PubChem CID: 50938612
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
α-​D-​Glucopyranoside,O-​β-​D-​fructofuranosyl-​(2→1)​-​O-​β-​D-​fructofuranosyl-​(2→1)​-​O-​β-​D-​fructofuranosyl-​(2→1)​-​O-​β-​D-​fructofuranosyl-​(2→1)​-​β-​D-​fructofuranosyl
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
K412899-5mg
3
$125.90
10mg
K412899-10mg
2
$178.90
25mg
K412899-25mg
2
$357.90
50mg
K412899-50mg
2
$626.90
100mg
K412899-100mg
2
$992.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

1,1,1,1-Kestohexaose is a major DP 6 fructan in crested wheatgrass leaves.

Specifications

Synonyms
α-​D-​Glucopyranoside, O-​β-​D-​fructofuranosyl-​(2→1)​-​O-​β-​D-​fructofuranosyl-​(2→1)​-​O-​β-​D-​fructofuranosyl-​(2→1)​-​O-​β-​D-​fructofuranosyl-​(2→1)​-​β-​D-​fructofuranosyl
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
1, 1, 1, 1-Kestohexaose is a major DP 6 fructan in crested wheatgrass leaves.
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Product Properties
ALogP-11.499
HBD Count20
Rotatable Bond21
Names and Identifiers
Pubchem Sid504770978
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504770978
Canonical SmilesC(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)COC3(C(C(C(O3)CO)O)O)COC4(C(C(C(O4)CO)O)O)COC5(C(C(C(O5)CO)O)O)COC6(C(C(C(O6)CO)O)O)CO)O)O)O)O
IUPAC Name(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
InChIKeyBWRYDXSZCCQXIF-TWMOFSFSSA-N
INCHI1S/C36H62O31/c37-1-12-18(44)24(50)25(51)31(61-12)67-36(30(56)23(49)17(6-42)66-36)11-60-35(29(55)22(48)16(5-41)65-35)10-59-34(28(54)21(47)15(4-40)64-34)9-58-33(27(53)20(46)14(3-39)63-33)8-57-32(7-43)26(52)19(45)13(2-38)62-32/h12-31,37-56H,1-11H2/t12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24+,25-,26+,27+,28+,29+,30+,31-,32-,33-,34-,35-,36+/m1/s1
Isomeric SMILES C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@]2([C@H]([C@@H]([C@H](O2)CO)O)O)CO[C@]3([C@H]([C@@H]([C@H](O3)CO)O)O)CO[C@]4([C@H]([C@@H]([C@H](O4)CO)O)O)CO[C@]5([C@H]([C@@H]([C@H](O5)CO)O)O)CO[C@]6([C@H]([C@@H]([C@H](O6)CO)O)O)CO)O)O)O)O
PubChem CID 50938612
Molecular Weight 990.86

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 O-glycosyl compounds  C-glycosyl compounds  Ketals  Oxanes  Oxolanes  Secondary alcohols  Polyols  Oxacyclic compounds  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oligosaccharide - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Ketal - Oxane - Oxolane - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Hydrocarbon derivative - 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.

5 results found

Lot NumberCertificate TypeDateItem
K2228497Certificate of AnalysisSep 08, 2025 K412899
K2228563Certificate of AnalysisSep 08, 2025 K412899
K2228565Certificate of AnalysisSep 08, 2025 K412899
K2228566Certificate of AnalysisSep 08, 2025 K412899
K2228587Certificate of AnalysisSep 08, 2025 K412899
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 100 mg/mL (100.92 mM);    
DMSO(mg / mL) Max Solubility100
DMSO(mM) Max Solubility100.922431019518
Water(mg / mL) Max Solubility-1
Molecular Weight990.900 g/mol
XLogP3-11.100
Hydrogen Bond Donor Count20
Hydrogen Bond Acceptor Count31
Rotatable Bond Count21
Exact Mass990.328 Da
Monoisotopic Mass990.328 Da
Topological Polar Surface Area506.000 Ų
Heavy Atom Count67
Formal Charge0
Complexity1590.000
Isotope Atom Count0
Defined Atom Stereocenter Count25
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.