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S5200

Suberic acid

98%

Synonym(s):

Octanedioic acid

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About This Item

Linear Formula:

HOOC(CH₂)₆COOH

CAS Number:

Molecular Weight:

174.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

EC Number:

208-010-9

Beilstein/REAXYS Number:

1210161

MDL number:

Assay:

98%

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Properties

Quality Level

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

Description

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.

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pictograms

Exclamation mark

signalword

Warning

hcodes

pcodes

P264 - P280 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

flash_point_f

410.0 °F - closed cup

flash_point_c

210 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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)

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)

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)

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Global Trade Item Number

SKU	GTIN
S5200-100G	04061832491127
S5200-500G	04061832491134
S5200-5G	04061836945657