All Photos(4)
About This Item
Linear Formula:
HOOC(CH2)6COOH
CAS Number:
Molecular Weight:
174.19
Beilstein:
1210161
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
bp
230 °C/15 mmHg (lit.)
mp
139-146 °C
140-144 °C (lit.)
SMILES string
OC(=O)CCCCCCC(O)=O
InChI
1S/C8H14O4/c9-7(10)5-3-1-2-4-6-8(11)12/h1-6H2,(H,9,10)(H,11,12)
InChI key
TYFQFVWCELRYAO-UHFFFAOYSA-N
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Application
Suberic acid can be used to synthesize:
- Perfluorinated analogs of suberoyl anilide hydroxamic acid (SAHA) as potent histone deacetylase inhibitors.
- Hemiester analogs of pregnenolone sulfate (PES).
- Cellulose acetate suberate, a cellulose ω-carboxyalkanoate.
- It can also act as a cross-linker for poly(vinyl alcohol) (PVA). The cross-linked molecule shows enhanced tensile strength when compared to neat PVA.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
410.0 °F - closed cup
Flash Point(C)
210 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Perfluorinated HDAC inhibitors as selective anticancer agents.
Walton J W, et al.
Organic & Biomolecular Chemistry, 15(43), 9186-9190 (2017)
Rifampin stability and solution concentration enhancement through amorphous solid dispersion in cellulose ω-carboxyalkanoate matrices.
Arca H C, et al.
Journal of Pharmaceutical Sciences, 107(1), 127-138 (2018)
Positive Modulators of the N-Methyl-d-aspartate Receptor: Structure?Activity Relationship Study of Steroidal 3-Hemiesters.
Krausova B, et al.
Journal of Medicinal Chemistry, 61(10), 4505-4516 (2018)
Crosslinking of Polyvinyl Alcohol (PVA) and Effect of Crosslinker Shape (Aliphatic and Aromatic) Thereof.
Sonker A K, et al.
Journal of Polymers and the Environment, 26(5), 1782-1794 (2018)
Ronald J Nachman et al.
Peptides, 26(1), 115-120 (2005-01-01)
The aliphatic amino diacid alpha-aminosuberic acid can function as an effective, stable mimic of the hydrolysis-susceptible Tyr(SO3H) group in sulfakinin neuropeptide analogs for both hindgut contractile activity in cockroach and food intake-inhibition activity in the desert locust. In the analog
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