Dextran - Premium pure , CAS No.9004-54-0

CAS: 9004-54-0 Cat. No.: D490149 分子式: [C6H10O5]n 分子量: 270000 EC番号: 232-677-5
注文可能
%1のみ残っています
GRADE & PURITY Premium pure ? Premium pure grade combining high purity with premium QC. Use for high-stakes work needing both cleanliness and lot consistency.
Synonyms
D400717 | D400719 | D400725 | D400730 | D400759 | D400763 | D400765 | D400767 | D400771 | D400775 | D400777 | D400713 | D400779 | D400784 | D406300 | D400769 | DEX 500; Detrax 40; Dextranen; Dextraven | D1449 | B1999-079228 | FT-0776551 | BCP13568 | Dextr
Storage
Room temperature,Argon charged,Desiccated
Shipped In
Normal
価格
同じかそれ以下 $9.90 通常価格 $9.90
AVAILABLE TO ORDER

概要

Product specifications and parameters

ItemNameSpecificationsMolecular Weight
D490149-1500DextranPremium1500
D490149-3500DextranPremium3500
D490149-5000DextranPremium5000
D490149-6000DextranPremium6000
D490149-10KDextranPremium10000
D490149-20KDextranPremium20000
D490149-25KDextranPremium25000
D490149-40KDextranPremium40000
D490149-70KDextranPremium70000
D490149-150KDextranPremium150000
D490149-250KDextranPremium250000
D490149-1000DextranPremium1000
D490149-500KDextranPremium500000
D490149-750KDextranPremium750000
D490149-110KDextranPremium110000
D490149-60KDextranPremium60000

Dextran (also known as glucan) is a class of polysaccharides composed mainly of glucose units, specifically D-glucose units linked by α-(1-6) bonds. Its high molecular weight and specific structure depend on the microbial strain responsible for its production. This homogeneous polysaccharide is produced by the action of extracellular dextran sucrases, which are commonly found in lactic acid bacteria such as Leuconostoc, Lactobacillus, Streptococcus, Weissella, and Pediococcus. Dextran is versatile and widely used in fields such as biochemistry, cell biology, drug delivery research, and gel electrophoresis.
Dextran from Leuconostoc has been used:
To mix with embryo suspensions in seawater to prepare cryo-imaging samples
To cryofix zebrafish larvae by immersing their tails in water
In the synthesis of vinyl sulfone-modified dextran (DX-VS)
To synthesize methacrylate-functionalized dextran via an ester bond (DX-O-MeA)
As a supplement in NCTC-135 tissue culture medium to prepare perfusion medium
Dextran is a branched dextran composed of linear α(1→6) linked glucose units with branches initiated by α(1→3) linkages. The molecular weight of dextran ranges from 10,000 to 150,000 Kd. Dextran is used in a variety of applications as a volume expander, stabilizer, matrix component, binding platform, lubricant, and physical structural component.
Dextran 40 is used to develop improved preservation solutions for transplanted organs. Dextran 40 can be used to determine cell compactness and flux parameters between cell layers. Dextran 40 can be used as a colloidal plasma volume expander.
Biochemical/Physiological Actions
Osmotic Balance: Dextran helps maintain osmotic balance by increasing the concentration of solutes in a solution. This prevents excessive water from crossing the cell membrane, thereby maintaining cell integrity and function.
- Cryoprotection: Dextran acts as a cryoprotectant by forming a protective barrier around cells and tissues during freezing. This barrier inhibits the formation of ice crystals, which can damage cell membranes and structures.
-Viscosity control: Dextran can change the viscosity of a solution by increasing its molecular weight. This change in viscosity affects the fluidity of the solution, making it useful for controlling the consistency of solutions in various processes.
-Drug delivery: Modified dextran is used as a carrier for controlled drug delivery. Dextran can encapsulate drugs and release them gradually, increasing the solubility of the drug, controlling the release profile, and thus improving the therapeutic effect.
-Gel electrophoresis: Dextran can increase the density of the sample loading solution in gel electrophoresis. This increased density helps the sample sink into the gel matrix, allowing for more precise separation of molecules based on size and charge during electrophoresis.
-Enzyme stabilization: Dextran stabilizes enzymes by providing a protective environment. It forms a stable matrix around the enzyme, enhancing the enzyme's activity and extending its lifespan in various biochemical reactions. This protection prevents enzyme denaturation and inactivation, allowing the enzyme to function more effectively.

Specifications

同義語
D400717 | D400719 | D400725 | D400730 | D400759 | D400763 | D400765 | D400767 | D400771 | D400775 | D400777 | D400713 | D400779 | D400784 | D406300 | D400769 | DEX 500; Detrax 40; Dextranen; Dextraven | D1449 | B1999-079228 | FT-0776551 | BCP13568 | Dextr
仕様と純度
Premium pure
保管条件
Room temperature,Argon charged,Desiccated
入荷
Normal
等級
Premium pure
名前と識別子
パブケム・シド
パブケム・シド・ウル
https://pubchem.ncbi.nlm.nih.gov/substance/508816509
カノニカル・スマイル
C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC(C(C(C(C=O)O)O)O)O)O)O)O)O)O)O)O
IUPAC Name
2,3,4,5-tetrahydroxy-6-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyhexanal
InChIKey
FZWBNHMXJMCXLU-UHFFFAOYSA-N
INCHI
1S/C18H32O16/c19-1-5(21)9(23)10(24)6(22)3-31-17-16(30)14(28)12(26)8(34-17)4-32-18-15(29)13(27)11(25)7(2-20)33-18/h1,5-18,20-30H,2-4H2
異性体SMILES
C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC(C(C(C(C=O)O)O)O)O)O)O)O)O)O)O)O
WGKドイツ
2
分子量
270000
Reaxy-Rn
30920174
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=30920174&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
分類Fatty Acyls
SubclassFatty acyl glycosides
Intermediate Tree Nodes Not available
Direct ParentFatty acyl glycosides of mono- and disaccharides
Alternative Parents Alkyl glycosides  O-glycosyl compounds  Disaccharides  Oxanes  Beta-hydroxy aldehydes  Alpha-hydroxyaldehydes  Secondary alcohols  Polyols  Oxacyclic compounds  Acetals  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Beta-hydroxy aldehyde - Oxane - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aldehyde - Alcohol - Primary alcohol - Aliphatic heteromonocyclic compound
説明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 a small molecule
3 D構造
インタラクティブ化学構造モデル





証明書(CoA、COO、BSE/TSEと分析図)
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80 results found

Lot NumberCertificate Type日付商品
J2619184Certificate of AnalysisOct 08, 2026 D490149
J2619183Certificate of AnalysisOct 08, 2026 D490149
J2619182Certificate of AnalysisOct 08, 2026 D490149
J2614419Certificate of AnalysisSep 30, 2026 D490149
J2614418Certificate of AnalysisSep 30, 2026 D490149
J2614417Certificate of AnalysisSep 30, 2026 D490149
I2623375Certificate of AnalysisSep 09, 2026 D490149
I2623376Certificate of AnalysisSep 09, 2026 D490149
I2623409Certificate of AnalysisSep 09, 2026 D490149
H2612353Certificate of AnalysisAug 06, 2026 D490149
H2612354Certificate of AnalysisAug 06, 2026 D490149
H2612352Certificate of AnalysisAug 06, 2026 D490149
H2604446Certificate of AnalysisJul 27, 2026 D490149
H2604454Certificate of AnalysisJul 27, 2026 D490149
H2604447Certificate of AnalysisJul 27, 2026 D490149
G2613098Certificate of AnalysisJul 24, 2026 D490149
G2613119Certificate of AnalysisJul 24, 2026 D490149
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G2622251Certificate of AnalysisJul 07, 2026 D490149
G2622252Certificate of AnalysisJul 07, 2026 D490149
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A2616109Certificate of AnalysisJul 03, 2026 D490149
G2609411Certificate of AnalysisJun 17, 2026 D490149
G2609410Certificate of AnalysisJun 17, 2026 D490149
G2609409Certificate of AnalysisJun 17, 2026 D490149
F2622294Certificate of AnalysisJun 13, 2026 D490149
F2622292Certificate of AnalysisJun 13, 2026 D490149
G2228704Certificate of AnalysisJun 08, 2026 D490149
E2607370Certificate of AnalysisApr 22, 2026 D490149
E2607359Certificate of AnalysisApr 22, 2026 D490149
E2607351Certificate of AnalysisApr 22, 2026 D490149
A2616110Certificate of AnalysisJan 21, 2026 D490149
G2228713Certificate of AnalysisDec 22, 2025 D490149
L2518374Certificate of AnalysisDec 06, 2025 D490149
L2518373Certificate of AnalysisDec 06, 2025 D490149
G2228699Certificate of AnalysisNov 05, 2025 D490149
G2228670Certificate of AnalysisNov 05, 2025 D490149
J2528102Certificate of AnalysisNov 05, 2025 D490149
J2513035Certificate of AnalysisOct 20, 2025 D490149
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I2516080Certificate of AnalysisSep 24, 2025 D490149
G2320579Certificate of AnalysisSep 24, 2025 D490149
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I2518165Certificate of AnalysisSep 23, 2025 D490149
I2518166Certificate of AnalysisSep 23, 2025 D490149
H2527308Certificate of AnalysisAug 14, 2025 D490149
H2527309Certificate of AnalysisAug 14, 2025 D490149
G2521135Certificate of AnalysisJul 07, 2025 D490149
G2521134Certificate of AnalysisJul 07, 2025 D490149
G2521133Certificate of AnalysisJul 07, 2025 D490149
G2521345Certificate of AnalysisJul 03, 2025 D490149
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G2228708Certificate of AnalysisApr 11, 2025 D490149
C2507091Certificate of AnalysisMar 12, 2025 D490149
G2228710Certificate of AnalysisMar 11, 2025 D490149
G2228702Certificate of AnalysisDec 30, 2024 D490149
J2409034Certificate of AnalysisOct 19, 2024 D490149
G2320592Certificate of AnalysisNov 30, 2023 D490149
J2310579Certificate of AnalysisOct 17, 2023 D490149
J2310578Certificate of AnalysisOct 17, 2023 D490149
G2228706Certificate of AnalysisSep 07, 2023 D490149
G2228711Certificate of AnalysisSep 07, 2023 D490149
I2304113Certificate of AnalysisSep 06, 2023 D490149
G2228709Certificate of AnalysisAug 22, 2023 D490149
G2326055Certificate of AnalysisJul 31, 2023 D490149
G2320572Certificate of AnalysisJul 25, 2023 D490149
G2320580Certificate of AnalysisJul 25, 2023 D490149
G2320573Certificate of AnalysisJul 25, 2023 D490149
G2320587Certificate of AnalysisJul 25, 2023 D490149
F2310757Certificate of AnalysisJun 28, 2023 D490149
F2310758Certificate of AnalysisJun 28, 2023 D490149
F2610175Certificate of AnalysisMay 23, 2023 D490149
J2531064Certificate of AnalysisMay 23, 2023 D490149
E2317314Certificate of AnalysisMay 23, 2023 D490149
E2317319Certificate of AnalysisMay 22, 2023 D490149
B2626146Certificate of AnalysisMay 22, 2023 D490149
E2317326Certificate of AnalysisMay 22, 2023 D490149
E2317320Certificate of AnalysisMay 22, 2023 D490149
E2317317Certificate of AnalysisMay 22, 2023 D490149
E2317313Certificate of AnalysisMay 20, 2023 D490149
化学的性質と物理的性質
溶解度Soluble in water, DMSO, formamide, ethylene glycol and glycerol
感度moisture sensitive
比旋光度[α]197° (C=6,H2O)
分子量504.400 g/mol
XLogP3-7.200
Hydrogen Bond Donor Count11
Hydrogen Bond Acceptor Count16
Rotatable Bond Count11
Exact Mass504.169 Da
Monoisotopic Mass504.169 Da
Topological Polar Surface Area277.000 Ų
Heavy Atom Count34
Formal Charge0
Complexity625.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count14
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Citations of This Product
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