60930
Suberic acid
purum, ≥98.0% (T)
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:
≥98.0% (T)
InChI key
TYFQFVWCELRYAO-UHFFFAOYSA-N
InChI
1S/C8H14O4/c9-7(10)5-3-1-2-4-6-8(11)12/h1-6H2,(H,9,10)(H,11,12)
SMILES string
OC(=O)CCCCCCC(O)=O
grade
purum
assay
≥98.0% (T)
bp
230 °C/15 mmHg (lit.)
Quality Level
mp
140-144 °C
functional group
carboxylic acid
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
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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R J Truscott et al.
Clinica chimica acta; international journal of clinical chemistry, 94(1), 31-39 (1979-05-16)
The urine of a child who presented with an episode of a disease resembling Reye's syndrome was found to contain large quantities of the dicarboxylic acids adipic and suberic acids, as well as the glycine conjugate of suberic acid, suberyl
Xu Dong Zhang et al.
Biochemical pharmacology, 66(8), 1537-1545 (2003-10-14)
TRAIL appears to be a promising anticancer agent in that it induces apoptosis in a wide range of cancer cells but not normal tissues. Sensitivity of melanoma cells to TRAIL-induced apoptosis varied considerably because of their development of various resistance
S Hayakawa
Zeitschrift fur allgemeine Mikrobiologie, 22(5), 309-326 (1982-01-01)
Through the isolation and identification of a wide variety of degradation products formed from bile acids by microorganisms, a unified scheme for the complete degradation of bile acids to carbon dioxide and water has been proposed and discussed. The proposed
Larisa Sheihet et al.
Biomacromolecules, 6(5), 2726-2731 (2005-09-13)
We describe the synthesis and characterization of a family of biocompatible ABA-triblock copolymers that comprised of hydrophilic A-blocks of poly(ethylene glycol) and hydrophobic B-blocks of oligomers of suberic acid and desaminotyrosyl-tyrosine esters. The triblock copolymers spontaneously self-assemble in aqueous solution
Monica Ilies et al.
Bioorganic & medicinal chemistry, 11(10), 2227-2239 (2003-04-26)
Novel matrix metalloproteinase (MMP)/bacterial collagenase inhibitors are reported, considering the sulfonylated amino acid hydroxamates as lead molecules. A series of compounds was prepared by reaction of arylsulfonyl isocyanates with N-(5H-dibenzo[a,d]cyclohepten-5-yl)- and N-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl) methyl glycocolate, respectively, followed by the conversion of
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