Glycidol - ≥96%, used for Glycidol can be utilized for the synthesis of hyperbranched polyglycerol (hPG) through ring-opening reactions.Due to their thermal stability and oxidative stability, these hPGs are considered substitutes for PEG in the developmen

CAS: 556-52-5 Cat. No.: G106989 Formule: C3H6O2 Poids moléculaire: 74.08 Beilstein Registry Number: 383562 Numéro CE: 209-128-3
DISPONIBLE À COMMANDE
GRADE & PURITY ≥96%
Synonyms
3-Hydroxypropylene oxide | Glycide | 2,3-Epoxypropanol | Epoxypropyl alcohol | GLYCIDOL | 1-Propanol, 2,3-epoxy- | Allyl alcohol oxide | oxiran-2-ylmethanol | Oxiranemethanol | FT-0745851 | glycerol glycide | Monoepoxide glycidol | Tox21_300301 | 2-(Hydro
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
Size
Allemagne (EU)
USA*
Price
Qty
25g
G106989-25g
En stock ≥10
33,76€
100g
G106989-100g
1 En stock
49,37€
500g
G106989-500g
1 En stock
164,78€
Enter a quantity for the sizes you want to add.
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Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 97 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

An epoxide building block

It is completely miscible with water, low-carbon alcohols, esters, ketones, ether, benzene, toluene, styrene, chlorobenzene, chloromethane, chloroform, trichloroethylene, dimethylformamide, dimethyl sulfoxide, and acetonitrile, partially soluble in xylene, tetrachloroethylene, and 1,1,1-trichloroethane, and almost insoluble in aliphatic and cycloaliphatic hydrocarbons.Flammability at 415°C, viscosity (20°C) of 4.00 mPa·s, and surface tension of 45.3 mN/m (22°C).It can self-aggregate, and acids, alkalis, or salts can promote self-aggregation, even posing an explosion risk.

Specifications

Synonymes
3-Hydroxypropylene oxide | Glycide | 2,3-Epoxypropanol | Epoxypropyl alcohol | GLYCIDOL | 1-Propanol, 2,3-epoxy- | Allyl alcohol oxide | oxiran-2-ylmethanol | Oxiranemethanol | FT-0745851 | glycerol glycide | Monoepoxide glycidol | Tox21_300301 | 2-(Hydro
Spécifications et pureté
≥96%
Application
Glycidol can be utilized for the synthesis of hyperbranched polyglycerol (hPG) through ring-opening reactions.Due to their thermal stability and oxidative stability, these hPGs are considered substitutes for PEG in the development of anti-fouling surfaces
Conditions de stockage de stockage
Store at -20°C,Argon charged
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥96%
Noms et identifiants
Pubchem Sid528774632
Sourires canoniquesC1C(O1)CO
IUPAC Nameoxiran-2-ylmethanol
InChIKeyCTKINSOISVBQLD-UHFFFAOYSA-N
INCHI1S/C3H6O2/c4-1-3-2-5-3/h3-4H,1-2H2
Isomères SMILES C1C(O1)CO
WGK Allemagne 3
Numéro ONU 2810
Groupe d'emballage I
Poids moléculaire 74.08
Beilstein 383562
Reaxy-Rn 383562
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=383562&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.

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
SuperclassOrganoheterocyclic compounds
ClasseEpoxides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentEpoxides
Alternative Parents Oxacyclic compounds  Dialkyl ethers  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as epoxides. These are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).
External Descriptors epoxide - primary alcohol
Structure 3D
Modèle de structure chimique interactif





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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

26 results found

Lot NumberCertificate TypeDateArticle
G2616393Certificate of AnalysisJul 11, 2026 G106989
G2616392Certificate of AnalysisJul 11, 2026 G106989
F2610607Certificate of AnalysisJun 06, 2026 G106989
F2610606Certificate of AnalysisJun 06, 2026 G106989
F2610605Certificate of AnalysisJun 06, 2026 G106989
E2606284Certificate of AnalysisApr 25, 2026 G106989
E2606286Certificate of AnalysisApr 25, 2026 G106989
E2606239Certificate of AnalysisApr 25, 2026 G106989
L2511382Certificate of AnalysisDec 03, 2025 G106989
L2511381Certificate of AnalysisDec 03, 2025 G106989
L2511380Certificate of AnalysisDec 03, 2025 G106989
K2327324Certificate of AnalysisSep 04, 2025 G106989
F2509380Certificate of AnalysisMay 12, 2025 G106989
L2502112Certificate of AnalysisMay 12, 2025 G106989
L2502052Certificate of AnalysisMay 12, 2025 G106989
F2509381Certificate of AnalysisMay 12, 2025 G106989
K2427461Certificate of AnalysisNov 04, 2024 G106989
K2427463Certificate of AnalysisNov 04, 2024 G106989
K2203117Certificate of AnalysisAug 22, 2024 G106989
K2203133Certificate of AnalysisAug 22, 2024 G106989
G2405456Certificate of AnalysisJun 21, 2024 G106989
G2405455Certificate of AnalysisJun 21, 2024 G106989
I2025145Certificate of AnalysisAug 08, 2022 G106989
G2214527Certificate of AnalysisJun 17, 2022 G106989
G2214526Certificate of AnalysisJun 17, 2022 G106989
G2214523Certificate of AnalysisJun 17, 2022 G106989

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Propriétés chimiques et physiques
SolubilitéMiscible with water, easily soluble in alcohols and ethers.
SensibilitéMoisture sensitive
Indice de réfraction1.4311
Point d'éclair (°C)71.5℃
Point d'ébullition (°C)61-62 °C/15 mmHg
Point de fusion (°C)-53℃
Poids moléculaire74.080 g/mol
XLogP3-0.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass74.0368 Da
Monoisotopic Mass74.0368 Da
Topological Polar Surface Area32.800 Ų
Heavy Atom Count5
Formal Charge0
Complexity35.900
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Références
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3. Yingdong Wu, Lu Bai, Junping Zheng.  (2023)  A robust and efficiently reprocessable poly(dimethylsiloxane) elastomers enhanced by self-catalysis Zn(II)-ligand bonds and silyl ethers.  JOURNAL OF POLYMER SCIENCE,  62  (5): (870-879).  [PMID:] [10.1002/pol.20230431]
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18. Zihao Wang, Jinxiang Yang, Wei Xiao, Tianyou Chen, Changfeng Yi, Zushun Xu.  (2022)  Engineering of polystyrene-supported artificial catalytic triad constructed by nanoprecipitation for efficient ester hydrolysis in water.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2022.128902]
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47. Shen Yanyu, He Guijin, Guo Yongsheng, Xie Hujun, Fang Wenjun.  (2017)  Modified Hyperbranched Polyglycerol as Dispersant for Size Control and Stabilization of Gold Nanoparticles in Hydrocarbons.  Nanoscale Research Letters,  12  (1): (1-9).  [PMID:28875345] [10.1186/s11671-017-2296-1]
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49. Haiyang Liao, Haiyan Zhang, Gai Qin, Zhenghui Li, Liuqing Li, Haoqun Hong.  (2017)  A macro-porous graphene oxide-based membrane as a separator with enhanced thermal stability for high-safety lithium-ion batteries.  RSC Advances,  (36): (22112-22120).  [PMID:] [10.1039/C7RA02950K]
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