49670
Glutaric anhydride
technical, ≥90% (NT)
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About This Item
Empirical Formula (Hill Notation):
C5H6O3
CAS Number:
Molecular Weight:
114.10
EC Number:
203-593-6
UNSPSC Code:
12162002
PubChem Substance ID:
Beilstein/REAXYS Number:
110051
MDL number:
grade
technical
assay
≥90% (NT)
bp
150 °C/10 mmHg (lit.)
mp
50-55 °C (lit.), 51-55 °C
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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Other Notes
This product has been replaced by G3806-ALDRICH | Glutaric anhydride 95%
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
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
Regulatory Information
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R L Bowen et al.
Journal of dental research, 79(4), 905-911 (2000-06-01)
Polymerizable cyclodextrin derivatives (PCDs) have been proposed as candidates for use in dental therapeutics (Bowen, 1996; Bowen and Reed, 1997). Here, PCD "libraries" were synthesized by quasi-random reactions of 6 moles of methacrylic anhydride plus 6 moles of cyclic glutaric
W L Shelver et al.
Journal of immunoassay, 21(1), 1-23 (2000-05-11)
Antibody generated from ractopamine-hemiglutarate-KLH was used to develop a ractopamine ELISA. The antibody showed good sensitivity in phosphate buffer, with an IC50 of 4.2 ng/ml (ppb) toward ractopamine and 16.2 ng/ml toward glucuronides of ractopamine conjugated to the phenethanolamine phenol
Rüdiger Benters et al.
Nucleic acids research, 30(2), E10-E10 (2002-01-15)
The DNA microarray-based analysis of single nucleotide polymorphisms (SNPs) is important for the correlation of genetic variations and individual phenotypes, and for locating disease-causing genes. To facilitate the development of surfaces suitable for immobilization of oligonucleotides, we report here a
H B Lazrek et al.
Nucleosides, nucleotides & nucleic acids, 26(8-9), 1103-1106 (2007-12-07)
We report the synthesis of homo and heterodimers of 3TC conjugates. All new dimers were screened for their ability to inhibit HIV-1 in MT4 cell line and were compared to AZT alone and showed marked antiviral activity.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 473448-1G | 04061826233726 |
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