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Merck
CN

S5200

Sigma-Aldrich

Suberic acid

98%

Synonym(s):

Octanedioic acid

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About This Item

Linear Formula:
HOOC(CH2)6COOH
CAS Number:
505-48-6
Molecular Weight:
174.19
Beilstein:
1210161
EC Number:
208-010-9
MDL number:
MFCD00004428
UNSPSC Code:
12352100
PubChem Substance ID:
24899642
NACRES:
NA.22

Key Documents

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Quality Level

200

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ2896
0000460029
0000460029
0000447403
0000447403

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Perfluorinated HDAC inhibitors as selective anticancer agents.
Walton J W, et al.
Organic & Biomolecular Chemistry, 15(43), 9186-9190 (2017)
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
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)
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