Suberic acid - CAS 505-48-6
Catalog: |
BB027107 |
Product Name: |
Suberic acid |
CAS: |
505-48-6 |
Synonyms: |
octanedioic acid |
IUPAC Name: | octanedioic acid |
Description: | Suberic acid (CAS# 505-48-6) is used in the preparation of reduction-sensitive micelles affecting their cellular uptake. This has potential application in delivery of anticancer drugs. It is also used in the fluorescent detection of amidinium-carboxylate and amidinium formation. |
Molecular Weight: | 174.19 |
Molecular Formula: | C8H14O4 |
Canonical SMILES: | C(CCCC(=O)O)CCC(=O)O |
InChI: | 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 |
Boiling Point: | 230 °C (15 mmHg) |
Melting Point: | 144 °C |
Density: | 1.162 g/cm3 |
Solubility: | 11.9 mg/mL |
Appearance: | Other solid |
MDL: | MFCD00004428 |
LogP: | 1.49620 |
GHS Hazard Statement: | H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] |
Precautionary Statement: | P264+P265, P280, P305+P351+P338, and P337+P317 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
US-2021087191-A1 | SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-a]ISOQUINOLIN-2-OL COMPOUNDS, THEIR SYNTHESIS, AND USE THEREOF | 20201204 |
EP-3763769-A1 | Method for preparing copolyamide resin and copolyamide hot-melt yarn | 20201109 |
US-10934384-B1 | Polyurethane elastomer compositions, and processes thereof | 20200909 |
US-10934385-B1 | Polyurethane elastomers, bio-additive foam compositions | 20200909 |
US-10988479-B1 | Morphic forms of trilaciclib and methods of manufacture thereof | 20200615 |
PMID | Publication Date | Title | Journal |
24374570 | 20140303 | Metabonomic analysis of quercetin against the toxicity of chronic exposure to low-level dichlorvos in rats via ultra-performance liquid chromatography-mass spectrometry | Toxicology letters |
23280859 | 20140201 | Metabonomics evaluation of urine from rats administered with phorate under long-term and low-level exposure by ultra-performance liquid chromatography-mass spectrometry | Journal of applied toxicology : JAT |
22821849 | 20121001 | Cannabinoid receptor antagonist-induced striated muscle toxicity and ethylmalonic-adipic aciduria in beagle dogs | Toxicological sciences : an official journal of the Society of Toxicology |
22884955 | 20120930 | Metabonomics analysis of urine and plasma from rats given long-term and low-dose dimethoate by ultra-performance liquid chromatography-mass spectrometry | Chemico-biological interactions |
22447321 | 20120501 | Bidirectional solid phase synthesis of a model oligoglycine bolaamphiphile and purification by rapid self-assembly | Journal of peptide science : an official publication of the European Peptide Society |
Complexity: | 135 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 174.08920892 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 174.08920892 |
Rotatable Bond Count: | 7 |
Topological Polar Surface Area: | 74.6 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS