Chitosan - low viscosity ,<200 mPa.s , CAS No.9012-76-4

CAS: 9012-76-4 Cat. No.: C105801 Formula: (C6H11NO4)n EC Number: 618-480-0
AVAILABLE TO ORDER
GRADE & PURITY low viscosity ,<200 mPa.s
Synonyms
Kytex M | Toluene, o-chloro- | Chitopearl BCW 3505 | Chitopearl BCW 2500 | YEA | Toluene, o-bromo- | AKOS037652919 | Chitopearl BCW 3507 | Chitosan | Sea Cure F | Q408510 | AKOS015918343 | N-[(2S,3R,4R,5S,6R)-5-[[(2S,3R,4R,5S,6R)-3-amino-5-[[(2S,3R,4R,5S,
Storage
Room temperature
Shipped In
Normal
★
Size
Germany (EU)
USA*
Price
Qty
25g
C105801-25g
—
3 In stock
€16.40
100g
C105801-100g
—
1 In stock
€37.23
250g
C105801-250g
1 In stock
1 In stock
€76.27
500g
C105801-500g
—
2 In stock
€128.34
Enter a quantity for the sizes you want to add.
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Why this grade

low viscosity ,<200 mPa.s 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 3045 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Flocculant, protein precipitation, encapsulating agent and aqueous thickener. Forms gels with multivalent anions. Gives clear solutions that dry to strong, clear films.

Specifications

Synonyms
Kytex M | Toluene, o-chloro- | Chitopearl BCW 3505 | Chitopearl BCW 2500 | YEA | Toluene, o-bromo- | AKOS037652919 | Chitopearl BCW 3507 | Chitosan | Sea Cure F | Q408510 | AKOS015918343 | N-[(2S,3R,4R,5S,6R)-5-[[(2S,3R,4R,5S,6R)-3-amino-5-[[(2S,3R,4R,5S,
Specifications & Purity
low viscosity ,<200 mPa.s
Storage
Room temperature
Shipped In
Normal
Names and Identifiers
Pubchem Sid508813170
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/508813170
IUPAC Namemethyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate
InChIKeyFLASNYPZGWUPSU-SICDJOISSA-N
INCHI1S/C56H103N9O39/c1-87-56(86)65-28-38(84)46(19(10-74)96-55(28)104-45-18(9-73)95-49(27(64)37(45)83)97-39-12(3-67)88-47(85)20(57)31(39)77)103-54-26(63)36(82)44(17(8-72)94-54)102-53-25(62)35(81)43(16(7-71)93-53)101-52-24(61)34(80)42(15(6-70)92-52)100-51-23(60)33(79)41(14(5-69)91-51)99-50-22(59)32(78)40(13(4-68)90-50)98-48-21(58)30(76)29(75)11(2-66)89-48/h11-55,66-85H,2-10,57-64H2,1H3,(H,65,86)/t11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48+,49+,50+,51+,52+,53+,54+,55+/m1/s1
Isomeric SMILES COC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)N)O[C@@H]3[C@H](O[C@H]([C@@H]([C@H]3O)N)O)CO)CO)CO)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O[C@H]9[C@@H]([C@H]([C@@H]([C@H](O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O

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 Aminoglycosides  O-glycosyl compounds  Oxanes  Methylcarbamates  1,2-aminoalcohols  Secondary alcohols  Hemiacetals  Organic carbonic acids and derivatives  Acetals  Oxacyclic compounds  Monoalkylamines  Primary alcohols  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  Organopnictogen compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oligosaccharide - Aminoglycoside core - Glycosyl compound - O-glycosyl compound - Amino saccharide - Oxane - Methylcarbamate - Carbamic acid ester - 1,2-aminoalcohol - Secondary alcohol - Hemiacetal - Carbonic acid derivative - Acetal - Oxacycle - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Primary alcohol - Primary aliphatic amine - Primary amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Amine - Alcohol - Organopnictogen compound - 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
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.

33 results found

Lot NumberCertificate TypeDateItem
F2206135Certificate of AnalysisMar 18, 2026 C105801
F2206133Certificate of AnalysisMar 18, 2026 C105801
H2613397Certificate of AnalysisMar 07, 2026 C105801
H2613377Certificate of AnalysisMar 07, 2026 C105801
H2613355Certificate of AnalysisMar 07, 2026 C105801
H2613354Certificate of AnalysisMar 07, 2026 C105801
C2613417Certificate of AnalysisMar 07, 2026 C105801
C2613424Certificate of AnalysisMar 07, 2026 C105801
C2613442Certificate of AnalysisMar 07, 2026 C105801
C2613443Certificate of AnalysisMar 07, 2026 C105801
H2613227Certificate of AnalysisMar 07, 2026 C105801
F2517279Certificate of AnalysisJun 04, 2025 C105801
F2517280Certificate of AnalysisJun 04, 2025 C105801
F2517281Certificate of AnalysisJun 04, 2025 C105801
F2517282Certificate of AnalysisJun 04, 2025 C105801
F2517422Certificate of AnalysisJun 04, 2025 C105801
L2511089Certificate of AnalysisJun 04, 2025 C105801
L2511098Certificate of AnalysisJun 04, 2025 C105801
A2503666Certificate of AnalysisDec 16, 2024 C105801
A2509009Certificate of AnalysisDec 16, 2024 C105801
A2509008Certificate of AnalysisDec 16, 2024 C105801
A2509007Certificate of AnalysisDec 16, 2024 C105801
A2503665Certificate of AnalysisDec 16, 2024 C105801
F2206134Certificate of AnalysisMar 18, 2022 C105801
F2206129Certificate of AnalysisMar 18, 2022 C105801
F2206125Certificate of AnalysisMar 18, 2022 C105801
E2407034Certificate of AnalysisMar 18, 2022 C105801
D2407078Certificate of AnalysisMar 18, 2022 C105801
B2306825Certificate of AnalysisMar 18, 2022 C105801
G2117160Certificate of AnalysisJul 03, 2021 C105801
G2117235Certificate of AnalysisJul 03, 2021 C105801
C2414049Certificate of AnalysisJul 03, 2021 C105801
K2211385Certificate of AnalysisJul 03, 2021 C105801
Chemical and Physical Properties
Melt Point(°C)102.5°C
Molecular Weight1526.500 g/mol
XLogP3-21.400
Hydrogen Bond Donor Count29
Hydrogen Bond Acceptor Count47
Rotatable Bond Count27
Exact Mass1525.64 Da
Monoisotopic Mass1525.64 Da
Topological Polar Surface Area808.000 Ų
Heavy Atom Count104
Formal Charge0
Complexity2630.000
Isotope Atom Count0
Defined Atom Stereocenter Count45
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Phthaloyl: Its Role in Primary Amine Protection and Practical Considerations for Experimental Selection
Research Value of Polyelectrolyte Multilayers: Layer-by-Layer Design of Interfacial Composition, Mass Transport, and Function
Key Judgments in Medical Hydrogel R&D: From Polymer Source and Crosslinking Strategy to Sterilization Planning, Scale-Up Feasibility, and Quality Control
Injectable Thermosensitive Gels: Gelation Behavior, Rheological Properties, and Drug Release Characteristics
Applications of Enzymatic Protein Crosslinking Systems in Gel Construction and Functional Evaluation
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From Natural Cellulose to Nanocrystals: Structural Characteristics, Application Directions, and Industrialization Challenges of CNC
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Signal Transduction Mechanism of Graphene Biosensors: From Molecular Recognition to Electrical/Optical Signal Readout and Materials Selection
Structure, Properties, and Mechanisms of Powdered Fragrances and Fragrance Delivery Materials: Stability, Release Mechanisms, and Selection Logic
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How Arbutin Regulates Melanin Production: α/β Anomeric Configuration and Tyrosinase Action
Niacinamide Brightening Mechanisms and Formulation Design: Melanosome Transfer, pH Regulation, and Combination Strategies
Citations of This Product
Solution Calculators
Reviews

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