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n-Dodecyl β-D-maltoside - Bioreagent Plus, ≥98%, high purity , CAS No.69227-93-6

8 Citations

COA

Grade & Purity:

UltraBio™

Ultra pure

≥98%

Cas Number: 69227-93-6
Molecular Weight: 510.62
Beilstein Registry Number: 55318
MDL number: MFCD00043012
PubChem CID: 114880
PubChem SID: 504756729

In stock

Item Number

N475300

Grouped product items
SKU	Size	Availability	Price
N475300-250mg	250mg	3	$69.90
N475300-1g	1g	3	$199.90
N475300-5g	5g	1	$699.90

View related series

Carbohydrate Chemistry (9) Cell Cycle (2830)

Basic Description

Synonyms	n-Dodecyl-b-D-maltoside \| MFCD00043012 \| (2R,3R,4S,5S,6R)-2-((2R,3S,4R,5R,6R)-6-(dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol \| N-Dodecyl b-D-maltoside \| DS-6568 \| EN300-207344 \|
Specifications & Purity	UltraBio™, Ultra pure, ≥98%
Storage Temp	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.
Grade	Ultra pure, UltraBio™
Product Description	n-Dodecyl β-D-maltoside is a non-ionic surfactant belonging to the alkyl polyglucoside family.n-Dodecyl β-D-maltoside has been used in a study to assess the effect of detergents on the thermal behavior of elastin-like polypeptides (ELP). It has also been used in a study to investigate how membrane structures will respond to detergent solubilization from amino acid sequences.Non-ionic detergent for the stabilization and activation of enzymes and for membrane research.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Fatty Acyls
    - Subclass Fatty acyl glycosides

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Fatty Acyls
Subclass	Fatty acyl glycosides
Intermediate Tree Nodes	Not available
Direct Parent	Fatty acyl glycosides of mono- and disaccharides
Alternative Parents	Alkyl glycosides O-glycosyl compounds Disaccharides Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Oxane - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
External Descriptors	disaccharide derivative - glycoside
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504756729
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756729
IUPAC Name	(2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-dodecoxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
INCHI	InChI=1S/C24H46O11/c1-2-3-4-5-6-7-8-9-10-11-12-32-23-21(31)19(29)22(16(14-26)34-23)35-24-20(30)18(28)17(27)15(13-25)33-24/h15-31H,2-14H2,1H3/t15-,16-,17-,18+,19-,20-,21-,22-,23-,24-/m1/s1
InChIKey	NLEBIOOXCVAHBD-QKMCSOCLSA-N
Smiles	CCCCCCCCCCCCOC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O
Isomeric SMILES	CCCCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)O
WGK Germany	3
Molecular Weight	510.62
Beilstein	55318
Reaxy-Rn	22092137
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=22092137&ln=

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.

11 results found

Lot Number	Certificate Type	Date	Item
E2528537	Certificate of Analysis	May 08, 2025	N475300
E2528582	Certificate of Analysis	May 08, 2025	N475300
D2510445	Certificate of Analysis	Mar 22, 2025	N475300
D2510446	Certificate of Analysis	Mar 22, 2025	N475300
C2315584	Certificate of Analysis	Feb 27, 2023	N475300
C2315547	Certificate of Analysis	Feb 27, 2023	N475300
C2315573	Certificate of Analysis	Feb 27, 2023	N475300
C2315596	Certificate of Analysis	Feb 27, 2023	N475300
C2315537	Certificate of Analysis	Feb 27, 2023	N475300
C2315540	Certificate of Analysis	Feb 27, 2023	N475300
L2403054	Certificate of Analysis	Feb 27, 2023	N475300

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Chemical and Physical Properties

Sensitivity	Heat sensitive；Moisture sensitive
Melt Point(°C)	224-226°C
Molecular Weight	510.600 g/mol
XLogP3	1.400
Hydrogen Bond Donor Count	7
Hydrogen Bond Acceptor Count	11
Rotatable Bond Count	16
Exact Mass	510.304 Da
Monoisotopic Mass	510.304 Da
Topological Polar Surface Area	179.000 Å²
Heavy Atom Count	35
Formal Charge	0
Complexity	554.000
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	1

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