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G3806

Sigma-Aldrich

Glutaric anhydride

95%

Synonym(s):

Pentanedioic anhydride

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About This Item

Empirical Formula (Hill Notation):
C5H6O3
CAS Number:
108-55-4
Molecular Weight:
114.10
Beilstein/REAXYS Number:
110051
EC Number:
203-593-6
MDL number:
MFCD00006679
UNSPSC Code:
12162002
PubChem Substance ID:
24895139
NACRES:
NA.23

Quality Level

200

assay

95%

SMILES string

O=C1CCCC(=O)O1

InChI

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

InChI key

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).

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

347.0 °F - closed cup

flash_point_c

175 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD6303V
WXBD5769V
WXBD4977V
WXBD3631V
WXBD1760V

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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
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
T Tanaka et al.
Biological & pharmaceutical bulletin, 16(12), 1270-1275 (1993-12-01)
The tumor distribution and the disposition of serum proteins, such as albumin, fetuin, transferrin, and IgG, were investigated in mice bearing Sarcoma 180. Serum proteins labeled with fluoresceinisothiocyanate (FITC) were administered to the mice. The FITC-labeled proteins acylated with glutaric
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
Jaleh Varshosaz et al.
Journal of drug targeting, 19(2), 140-153 (2010-05-01)
An oral colon-targeted formulation of budesonide was developed for treatment of ulcerative colitis. Budesonide conjugates were prepared using glutarate spacer and different molecular weights (MW) of dextran and their degree of substitution (DS), solubility, and stability were examined. Drug release
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