S5200
Suberic acid
98%
동의어(들):
Octanedioic acid
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
HOOC(CH2)6COOH
CAS 번호:
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%
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
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
저장 등급
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
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)