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G3806

Sigma-Aldrich

Glutaric anhydride

95%

Synonyme(s) :

Pentanedioic anhydride

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About This Item

Formule empirique (notation de Hill):
C5H6O3
Numéro CAS:
108-55-4
Poids moléculaire :
114.10
Numéro Beilstein :
110051
Numéro CE :
203-593-6
Numéro MDL:
MFCD00006679
Code UNSPSC :
12162002
ID de substance PubChem :
24895139
Nomenclature NACRES :
NA.23

Niveau de qualité

200

Pureté

95%

Chaîne SMILES 

O=C1CCCC(=O)O1

InChI

1S/C5H6O3/c6-4-2-1-3-5(7)8-4/h1-3H2

Clé InChI

VANNPISTIUFMLH-UHFFFAOYSA-N

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Application

  • Esterification mechanism of bagasse modified with glutaric anhydride in 1-allyl-3-methylimidazolium chloride: This study explores the homogenous esterification of bagasse with glutaric anhydride, providing insight into the effects of glutaric anhydride dosage on the process (H Wang et al., 2017).
  • Epoxy-anhydride vitrimers from aminoglycidyl resins with high glass transition temperature and efficient stress relaxation: Discusses the use of glutaric anhydride as a hardener in high-performance epoxy-based composites, comparing its effectiveness with other hardeners (M Giebler et al., 2020).
  • Effects of glutaric anhydride functionalization on filler-free benzoxazine/epoxy copolymers with shape memory and self-healing properties under near-infrared light: Examines how glutaric anhydride enhances the properties of copolymers, particularly in terms of shape memory and self-healing capabilities (L Amornkitbamrung et al., 2022).
  • Surface analysis and thermal behavior of the functionalized cellulose by glutaric anhydride through a solvent-free and catalyst-free process: Investigates the modification of cellulose using glutaric anhydride and analyzes its impact on thermal behavior and surface properties (H Fahim et al., 2023).
  • Cyclic anhydrides as powerful tools for bioconjugation and smart delivery: This article reviews the use of glutaric anhydride in bioconjugation, highlighting its potential in creating smart delivery systems for biologically active compounds (MV Spanedda et al., 2021).

Pictogrammes

CorrosionExclamation mark
GHS05,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302,H315,H318

Classification des risques

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

347.0 °F - closed cup

Point d'éclair (°C)

175 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Xinli Guo et al.
Molecules (Basel, Switzerland), 25(11) (2020-06-10)
In order to enhance the sensitivity of drug-resistant ovarian cancer cells to cisplatin (DDP), a co-delivery system was designed for simultaneous delivery of curcumin (CUR) and p53 DNA. Firstly, the bifunctional peptide K14 composed of tumor targeting peptide (tLyP-1) and
Dana Luca Motoc et al.
Polymers, 13(4) (2021-02-07)
This contribution focuses on the development of flax and flax/basalt hybrid reinforced composites based on epoxidized linseed oil (ELO) resin, exploiting the feasibility of different ratios of glutaric anhydride (GA) to maleinized linseed oil (MLO) in the hardener system (50:0
Rhodium-catalyzed enantioselective desymmetrization of meso-3,5-dimethyl glutaric anhydride: a general strategy to syn-deoxypolypropionate synthons.
Matthew J Cook et al.
Journal of the American Chemical Society, 129(30), 9302-9303 (2007-07-12)
B Ballantyne et al.
Veterinary and human toxicology, 34(6), 493-497 (1992-12-01)
Glutaric anhydride (GA), an industrial chemical, was found of moderate acute peroral lethal toxicity with LD50 values (95% confidence limits) in the rat of 1.41 (0.80-2.49) g/kg (males) and 0.54 (0.36-0.79) g/kg (females), with death being due in part to
Purushothaman Gopinath et al.
Organic letters, 14(5), 1358-1361 (2012-02-22)
We describe the desymmetrization of meso-glutaric anhydrides to chiral hemiesters using a bench-stable homodinuclear Ni(2)-(Schiff base) complex as the catalyst in good to excellent yield (up to 99%) and enantioselectivity (up to 94%). Using the opposite enantiomer of the catalyst
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