Skip to Content
Merck
CN

60930

Suberic acid

purum, ≥98.0% (T)

Synonym(s):

Octanedioic acid

Sign In to View Organizational & Contract Pricing.

Select a Size


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:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Suberic acid, purum, ≥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.)

mp

140-144 °C (lit.)
140-144 °C

functional group

carboxylic acid

Quality Level

Looking for similar products? Visit Product Comparison Guide

pictograms

Exclamation mark

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
Jomana Elaridi et al.
The Journal of organic chemistry, 71(20), 7538-7545 (2006-09-26)
A method to facilitate regioselective formation of multiple dicarba isosteres of cystine is described. A sequence of ruthenium-catalyzed cross metathesis and rhodium-catalyzed hydrogenation of nonproteinaceous allylglycine derivatives has been developed to achieve high-yielding and unambiguous formation of diaminosuberic acid derivatives.
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
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
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service