2-Hydroxyethyl cellulose(HEC) - average Mw~380,000 , CAS No.9004-62-0

CAS: 9004-62-0 Cat. No.: H434475 EC Number: 618-387-5
AVAILABLE TO ORDER
GRADE & PURITY average Mw~380,000
Synonyms
H11622 | Hydroxyethyl-cellulose | 2-Hydroxyethyl cellulose | DTXSID60873934 | 2-O-(2-Hydroxyethyl)-4-O-methylhexopyranosyl-(1->4)-[4-O-methylhexopyranosyl-(1->6)]hexopyranosyl-(1->5)-2,6-anhydro-1-deoxyheptitol | FT-0627136 | SCHEMBL23306563 | Hydroxyethy
Storage
Room temperature
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Size
Status
Price
Qty
25g
H434475-25g
5

$105.90

$123.90
Save $18.00 (14.53%)
500g
H434475-500g
1

$390.90

$456.90
Save $66.00 (14.45%)
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Why this grade

average Mw~380,000 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 204 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

2-Hydroxyethyl cellulose (HEC) is a water soluble biopolymer that is majorly used as a thickener and an adhesive. It has water retention which also includes good film forming ability for protective covering. Non-ionic water soluble polymer. Aqueous solutions are pseudoplastic. Readily disperses without lumping.


Application

Thickener, protective colloid, binder, stabilizer and suspending agent.

Specifications

Synonyms
H11622 | Hydroxyethyl-cellulose | 2-Hydroxyethyl cellulose | DTXSID60873934 | 2-O-(2-Hydroxyethyl)-4-O-methylhexopyranosyl-(1->4)-[4-O-methylhexopyranosyl-(1->6)]hexopyranosyl-(1->5)-2, 6-anhydro-1-deoxyheptitol | FT-0627136 | SCHEMBL23306563 | Hydroxyethy
Specifications & Purity
average Mw~380, 000
Storage
Room temperature
Names and Identifiers
Canonical SmilesCC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)OC)O)O)OC4C(C(C(C(O4)CO)OC)O)OCCO)O)O)O)O
IUPAC Name5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol
InChIKeyCWSZBVAUYPTXTG-UHFFFAOYSA-N
INCHI1S/C29H52O21/c1-10-15(34)16(35)24(13(8-33)45-10)49-28-20(39)18(37)25(50-29-26(43-5-4-30)21(40)23(42-3)12(7-32)47-29)14(48-28)9-44-27-19(38)17(36)22(41-2)11(6-31)46-27/h10-40H,4-9H2,1-3H3
Isomeric SMILES CC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)OC)O)O)OC4C(C(C(C(O4)CO)OC)O)OCCO)O)O)O)O
WGK Germany 1
RTECS FJ5958000
Reaxy-Rn 24866087
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24866087&ln=

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.

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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
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentOligosaccharides
Alternative Parents O-glycosyl compounds  Oxanes  Secondary alcohols  Oxacyclic compounds  Dialkyl ethers  Acetals  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oligosaccharide - O-glycosyl compound - Glycosyl compound - Oxane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Acetal - Hydrocarbon derivative - Primary alcohol - 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.

4 results found

Lot NumberCertificate TypeDateItem
C23111108Certificate of AnalysisDec 10, 2025 H434475
C23111111Certificate of AnalysisDec 10, 2025 H434475
G2510394Certificate of AnalysisDec 04, 2024 H434475
G2510422Certificate of AnalysisDec 04, 2024 H434475
Chemical and Physical Properties
Sensitivitymoisture sensitive
Melt Point(°C)288-290°C
Molecular Weight736.700 g/mol
XLogP3-7.700
Hydrogen Bond Donor Count11
Hydrogen Bond Acceptor Count21
Rotatable Bond Count15
Exact Mass736.3 Da
Monoisotopic Mass736.3 Da
Topological Polar Surface Area315.000 Ų
Heavy Atom Count50
Formal Charge0
Complexity999.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count20
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Microcrystalline Cellulose (MCC): A Comprehensive Primer and Selection Guide—Structural Features, Key Performance Metrics, and Application Scenarios
Understanding Hydrophilic Polymers in Aqueous Systems: Hydration Mechanisms, Structural Knobs, and Task-Oriented Selection Guide (Including Tables 1–3)
Applications and Selection of Acrylic Resins in Coatings: Analysis of Architectural, Industrial, and Supporting Materials
Natural Resins in Coating Formulations: Functional Positioning, Structure–Property Relationships, and Selection Validation
Waterborne Resin Technology Explained: Waterborne Forms, Performance Balance, and a Technology Map
Waterborne Resin Application Guide: Formulation Synergy, Troubleshooting, and Technology Development Trends
Why LABSA (Sulfonic Acid) Is Commonly Used in Household Cleaning Formulations: Neutralization Mechanism, Detergency Action, and Formulation Application Points
From Structure to Performance: Conditioning, Film-Forming, Thickening, and Chelating Applications of Functional Ingredients in Personal Care and Home Care
From Structure to Rheology: How Carbomer Forms Gel Structures and Enables Thickening, Suspension, and Auxiliary Emulsion Stabilization
What Is the Difference Between Triethanolamine and Diethanolamine: Understanding Their Formulation Functions, Application Differences, and Selection Logic from a Molecular-Structure Perspective
Thickening, Suspension, Auxiliary Stabilization, and Agglomeration Mechanisms of Xanthan Gum in Personal Care Formulations: From Molecular Structure to Processing Applications
AES (Fatty Alcohol Polyoxyethylene Ether Sulfate) in Personal and Home-Care Cleansing Formulations: An Analysis of Structure, Performance, and Low-Temperature Flowability
Understanding CAPB from Its Structure: How Cocamidopropyl Betaine Improves Foam, Enhances Mildness, and Supports Thickening
From Structure to Rheology: Thickening, Stabilization, and Selection Logic of Cellulose Ethers for Personal Care Applications
How to Select Thickeners for Strongly Acidic Cleaning Systems: Comparison of Thickening Mechanisms and Application Considerations for Fatty Amine Ethoxylates
Citations of This Product
References
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