Tridecanal - CAS 10486-19-8
Catalog: |
BB001495 |
Product Name: |
Tridecanal |
CAS: |
10486-19-8 |
Synonyms: |
tridecanal |
IUPAC Name: | tridecanal |
Description: | Tridecanal (CAS# 10486-19-8) is a model compound in the nonradioactive assay/RP-HPLC-fluorescence analysis of aliphatic aldehydes employing the Hantzsch reaction. |
Molecular Weight: | 198.34 |
Molecular Formula: | C13H26O |
Canonical SMILES: | CCCCCCCCCCCCC=O |
InChI: | InChI=1S/C13H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h13H,2-12H2,1H3 |
InChI Key: | BGEHHAVMRVXCGR-UHFFFAOYSA-N |
Boiling Point: | 269.53 °C (EPI 4.0) |
Melting Point: | 15°C |
Flash Point: | 112°C |
Purity: | 96.0 % |
Density: | 0.835 g/cm3 |
Solubility: | Insoluble in water; soluble in aclohol. |
Appearance: | Colorless liquid |
Storage: | Store tightly sealed under inert gas in a cool, well-ventilated area. |
MDL: | MFCD00007018 |
LogP: | 4.49630 |
Refractive Index: | 1.433 : 1.440 at 20 deg C |
GHS Hazard Statement: | H314 (17.91%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P261, P264, P271, P273, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P337+P313, P362, P363, P391, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113289695-A | Method for recovering hydroformylation catalyst | 20210621 |
CN-113372206-A | Method for synthesizing high-carbon aldehyde by using microchannel reaction device | 20210512 |
CN-113004111-A | Method for synthesizing (R) -psylla chinensis sex pheromone | 20210208 |
CN-112886063-A | Application of functionalized carbon dots in lithium battery electrolyte | 20210203 |
KR-102242940-B1 | Method for preparing a non-reducing cleaning composition containing vegetable extracts and a non-reducing cleaning composition prepared thereby | 20210119 |
PMID | Publication Date | Title | Journal |
22970932 | 20121016 | Simulations of smog-chamber experiments using the two-dimensional volatility basis set: linear oxygenated precursors | Environmental science & technology |
22238638 | 20120101 | Functional evolution of duplicated odorant-binding protein genes, Obp57d and Obp57e, in Drosophila | PloS one |
21509392 | 20110607 | Potentially important nighttime heterogeneous chemistry: NO3 with aldehydes and N2O5 with alcohols | Physical chemistry chemical physics : PCCP |
21429630 | 20110601 | Synthesis of N-substituted 2-[(1E)-alkenyl]-4-(1H)-quinolone derivatives as antimycobacterial agents against non-tubercular mycobacteria | European journal of medicinal chemistry |
21548958 | 20110506 | The location of olfactory receptors within olfactory epithelium is independent of odorant volatility and solubility | BMC research notes |
Complexity: | 110 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 198.198365449 |
Formal Charge: | 0 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 198.198365449 |
Rotatable Bond Count: | 11 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 5.4 |
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