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About This Item
Linear Formula:
CH3OCO(CH2)3COOCH3
CAS Number:
Molecular Weight:
160.17
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
214-277-2
Beilstein/REAXYS Number:
1771444
MDL number:
Product Name
DBE-5 dibasic ester, 99%
InChI key
XTDYIOOONNVFMA-UHFFFAOYSA-N
InChI
1S/C7H12O4/c1-10-6(8)4-3-5-7(9)11-2/h3-5H2,1-2H3
SMILES string
COC(=O)CCCC(=O)OC
assay
99%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
93-95 °C/13 mmHg
96-103 °C/15 mmHg (lit.)
density
1.09 g/mL at 25 °C (lit.)
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Legal Information
DuPont product
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
228.2 °F - closed cup
flash_point_c
109.00 °C - closed cup
ppe
Eyeshields, Gloves
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Misa Kuroki et al.
iScience, 23(1), 100786-100786 (2020-01-07)
Metabolic switching and rewiring play a dynamic role in programmed cell differentiation. Many pathogenic microbes need to survive in nutrient-deficient conditions and use the glyoxylate cycle, an anaplerotic pathway of the tricarboxylic acid cycle, to produce carbohydrates. The plant pathogenic
L Alvarez et al.
Drug and chemical toxicology, 18(4), 295-314 (1995-11-01)
Dibasic esters (DBE) are a mixture of 3 carboxylic acid esters which are used in the paint and coatings industry. In this study, groups of pregnant Crl:CD BR rats were exposed to either 0.16, 0.4, or 1.0 mg DBE/L by
J P Turner et al.
British journal of pharmacology, 104(2), 445-451 (1991-10-01)
1. The effects of L-glutamate diethyl ester (GDEE) HCl, glutarate diethyl ester (GlrDEE) and glutarate dimethyl ester (GlrDME) on depolarizing responses to alpha-amino-3-hydroxy-5- methyl-4-isoxazolepropionate (AMPA), kainate (Kain), N-methyl-D-aspartate (NMDA) and quisqualate (Quis), and spontaneous paroxysmal discharges (SPDs) were examined. Experiments
M S Bogdanffy et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(1), 124-129 (1991-01-01)
Inhalation exposure of rats to dibasic esters revealed lesions of the nasal olfactory epithelium similar to those observed with other ester solvents. Female rats are more sensitive to these effects than are male rats. It has been proposed that carboxylesterase
J B Morris et al.
Toxicology and applied pharmacology, 108(3), 538-546 (1991-05-01)
Inhalation exposure of the male and female rat to high concentrations of a mixture of the dibasic esters dimethyl succinate (DMS), dimethyl glutarate (DMG), and dimethyl adipate (DMA) results in mild olfactory toxicity. This response is thought to be due
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