Synthetic agarose - High Resolution,PCR Grade , CAS No.9012-36-6

CAS: 9012-36-6 Cat. No.: S579073 Numero EC: 232-731-8 PubChem CID: 11966311
Disponibile su ordine
GRADE & PURITY High Resolution,PCR Grade
Synonyms
AKOS015916622 | MJQHZNBUODTQTK-WKGBVCLCSA-N | Agarose gel beads | Agarose | EINECS 232-731-8 | agarotetraose | CHEBI:2511 | [4)-3,6-An-alpha-L-Galp-(1->3)-beta-D-Galp-(1->]n | SCHEMBL1413225 | (2S,3R,4S,5R,6R)-2-[[(1S,3S,4S,5S,8R)-3-[(2S,3R,4S,5S,6R)-2-[[
Storage
Room temperature
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
5g
S579073-5g
Su ordinazione · 8–12 settimane

50,24€

76,27€
Salva 26,03 € (34.13%)
25g
S579073-25g
Su ordinazione · 8–12 settimane

173,46€

203,83€
Salva 30,37 € (14.90%)
100g
S579073-100g
Su ordinazione · 8–12 settimane

446,80€

724,48€
Salva 277,68 € (38.33%)
500g
S579073-500g
Su ordinazione · 8–12 settimane

1.785,72€

2.546,73€
Salva 761,01 € (29.88%)
Enter a quantity for the sizes you want to add.
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Why this grade

High Resolution,PCR Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 264 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
AKOS015916622 | MJQHZNBUODTQTK-WKGBVCLCSA-N | Agarose gel beads | Agarose | EINECS 232-731-8 | agarotetraose | CHEBI:2511 | [4)-3,6-An-alpha-L-Galp-(1->3)-beta-D-Galp-(1->]n | SCHEMBL1413225 | (2S,3R,4S,5R,6R)-2-[[(1S,3S,4S,5S,8R)-3-[(2S,3R,4S,5S,6R)-2-[[
Specifiche e purezza
High Resolution,PCR Grade
Condizioni di conservazione di stoccaggio
Room temperature
Spedito in
Normal
Nomi e identificatori
Sorrisi canoniciC1[C@H]2[C@H]([C@@H](O1)[C@@H]([C@@H](O2)O)O)O[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O[C@H]4[C@H]([C@H]5[C@@H]([C@@H](O4)CO5)O[C@H]6[C@@H]([C@H]([C@H]([C@H](O6)CO)O)O)O)O)O
IUPAC Name(2S,3R,4S,5R,6R)-2-[[(1S,3S,4S,5S,8R)-3-[(2S,3R,4S,5S,6R)-2-[[(1S,3R,4S,5S,8R)-3,4-dihydroxy-2,6-dioxabicyclo[3.2.1]octan-8-yl]oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-4-hydroxy-2,6-dioxabicyclo[3.2.1]octan-8-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
InChIKeyMJQHZNBUODTQTK-WKGBVCLCSA-N
INCHI1S/C24H38O19/c25-1-5-9(27)11(29)12(30)22(38-5)41-17-8-4-36-20(17)15(33)24(40-8)43-18-10(28)6(2-26)39-23(14(18)32)42-16-7-3-35-19(16)13(31)21(34)37-7/h5-34H,1-4H2/t5-,6-,7+,8+,9+,10+,11+,12-,13+,14-,15+,16-,17-,18+,19+,20+,21-,22+,23+,24+/m1/s1
Isomeri SMILES C1[C@H]2[C@H]([C@@H](O1)[C@@H]([C@@H](O2)O)O)O[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O[C@H]4[C@H]([C@H]5[C@@H]([C@@H](O4)CO5)O[C@H]6[C@@H]([C@H]([C@H]([C@H](O6)CO)O)O)O)O)O
CAS alternativo 39346-81-1
PubChem CID 11966311

Documentazione

📋 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
ClasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentOligosaccharides
Alternative Parents O-glycosyl compounds  1,4-dioxepanes  Oxanes  Oxolanes  Secondary alcohols  Hemiacetals  Polyols  Oxacyclic compounds  Dialkyl ethers  Acetals  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Oligosaccharide - Glycosyl compound - O-glycosyl compound - 1,4-dioxepane - Dioxepane - Oxane - Oxolane - Secondary alcohol - Hemiacetal - Acetal - Dialkyl ether - Oxacycle - Ether - Polyol - Organoheterocyclic compound - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteropolycyclic compound
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Punto di fusione (°C)62-68℃
Peso molecolare630.500 g/mol
XLogP3-6.500
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count19
Rotatable Bond Count8
Exact Mass630.201 Da
Monoisotopic Mass630.201 Da
Topological Polar Surface Area285.000 Ų
Heavy Atom Count43
Formal Charge0
Complexity946.000
Isotope Atom Count0
Defined Atom Stereocenter Count20
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Domande frequenti e articoli
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Five Key Structural Features of Plasmids
Immobilized Enzyme Technology and Its Applications in Biocatalysis
An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)
A Review of Ten Commonly Used Techniques for Detection, Quantification, and Interaction Analysis in Nucleic Acid Research
Understanding Hydrophilic Polymers in Aqueous Systems: Hydration Mechanisms, Structural Knobs, and Task-Oriented Selection Guide (Including Tables 1–3)
16 Frequently Asked Questions About Nourseothricin
GelRed Nucleic Acid Stain: Frequently Asked Questions
Deoxyribonuclease (DNase): DNA Hydrolytic Cleavage Properties, Methodological Value, and Multi-Context Applications
Micrococcal Nuclease (MNase): A Technical Review of Enzymatic Properties, Reaction Control, and Research and Biomanufacturing Applications
dsDNase-Mediated Hydrolysis of Double-Stranded DNA: Enzymatic Characteristics, Methodological Strategies, and Bioanalytical Applications
Key Judgments in Medical Hydrogel R&D: From Polymer Source and Crosslinking Strategy to Sterilization Planning, Scale-Up Feasibility, and Quality Control
Applications of Enzymatic Protein Crosslinking Systems in Gel Construction and Functional Evaluation
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Citations of This Product
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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