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Merck

60930

Sigma-Aldrich

Suberic acid

purum, ≥98.0% (T)

Sinónimos:

Octanedioic acid

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About This Item

Fórmula lineal:
HOOC(CH2)6COOH
Número de CAS:
Peso molecular:
174.19
Beilstein/REAXYS Number:
1210161
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

purum

Quality Level

assay

≥98.0% (T)

bp

230 °C/15 mmHg (lit.)

mp

140-144 °C (lit.)
140-144 °C

functional group

carboxylic acid

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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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

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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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
M Rivard et al.
Amino acids, 15(4), 389-392 (1999-01-19)
Papain-catalyzed regioselective cleavage of alpha-methyl ester in Z-DL-Asu(OMe)-OMe leads to Z-L-Asu(OMe)-OH and Z-D-Asu(OMe)-OMe. Subsequent saponifications yield Z-L-Asu-OH and Z-D-Asu-OH. The enzymatic alpha-ester hydrolysis was also achieved by subtilisin BPN' in organic solvent with low water content.
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
Taishi Yokoi et al.
Dalton transactions (Cambridge, England : 2003), 41(9), 2732-2737 (2012-01-18)
Octacalcium phosphates (OCPs) co-incorporated with various molar ratios of succinate and suberate ions were synthesized by wet processing. The interplanar spacings of the (100) planes (d(100)) of OCPs formed in the presence of succinic acid (Suc) or suberic acid (Sub)
Q Gao et al.
Acta crystallographica. Section B, Structural science, 50 ( Pt 6), 695-703 (1994-12-01)
Neutron diffraction data for suberic acid [HOOC(CH2)6COOH] were collected at 18.4, 75 and 123 K using a twinned crystal. The neutron data reduction included derivation of a complete set of corrected intensities, as if from a single crystal. This was

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