Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H22O4 |
| Molecular Weight | 230.3007 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOC(=O)CCC(=O)OCCCC
InChI
InChIKey=YUXIBTJKHLUKBD-UHFFFAOYSA-N
InChI=1S/C12H22O4/c1-3-5-9-15-11(13)7-8-12(14)16-10-6-4-2/h3-10H2,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Biodegradation of poly(tetramethylene succinate-co-tetramethylene adipate) and poly(tetramethylene succinate) through water-soluble products. | 2001 May |
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| Cloning and sequence analysis of poly(tetramethylene succinate) depolymerase from Acidovorax delafieldii strain BS-3. | 2002 |
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| Molecular structure of crude beeswax studied by solid-state 13C NMR. | 2004 |
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| Biodegradability of plastics. | 2009 Aug 26 |
Patents
Sample Use Guides
Groups of eight islets were each incubated for 90 min in 1.0 mL of a bicarbonate-buffered medium containing bovine serum albumin (5.0 mg/mL) and D-glucose (7.0 mM) and 10 mM of dibutyl succinate. The insulin released by the islets in the incubation medium was then assayed by a radioimmunological back titration. dibutyl succinate significantly augmented insulin release by +24.8 micor-U per in the 90 min incubation period.
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WHO-VATC |
QP53GX03
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EPA PESTICIDE CODE |
77802
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WHO-ATC |
P03BX04
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m143
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Q050512U41
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dibutyl succinate
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CHEMBL1788388
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141-03-7
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205-449-8
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DB13332
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ACTIVE MOIETY
