5-Methylundecane - CAS 1632-70-8

Catalog:	BB060364
Product Name:	5-Methylundecane
CAS:	1632-70-8
Synonyms:	NSC 158672; 1,2,3,4,6,7,8,8a-Octahydronaphthalene-1,6-diol

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	5-methylundecane
Description:	5-Methylundecane is a useful research chemical, an aroma compound derived from the thermal degradation of carotenoids in cashew apple juice models.
Molecular Weight:	170.33
Molecular Formula:	C12H26
Canonical SMILES:	CCCCCCC(C)CCCC
InChI:	InChI=1S/C12H26/c1-4-6-8-9-11-12(3)10-7-5-2/h12H,4-11H2,1-3H3
InChI Key:	QULNVKABFWNUCW-UHFFFAOYSA-N
References:	Zepka, L. Q., et al. Food Res. Int., 56, 108 (2014); Jeribi, C., et al. J. Essent. Oil Bear. Pl, 19, 1471 (2016).

Publication Number	Title	Priority Date
US-11187185-B1	Waste heat recovery lube oil management	20210405
CN-112495141-A	Method and system for collecting tobacco fragrance in flue-cured tobacco leaf tail gas	20201110
TW-I718986-B	Conductive polymer hybrid electrolytic capacitor	20201029
CN-114181530-A	Bioelectrode composition, bioelectrode, method for producing bioelectrode, and silicon material particle	20200915
EP-3968343-A2	Bio-electrode composition, bio-electrode, method for manufacturing bio-electrode, and silicon material particle	20200915
US-2022079461-A1	Bio-electrode composition, bio-electrode, method for manufacturing bio-electrode, and silicon material particle	20200915
WO-2022054569-A1	Argan extract manufacturing method, argan extract, hair growth promotion agent, hair loss prevention agent, and hair cycle regulation agent	20200909
CN-212300584-U	Collision indicating device	20200527
GB-2595047-A	Skin disinfectant	20200415
JP-2021164630-A	Bioelectrode composition, bioelectrode and method for manufacturing bioelectrode	20200401

PMID	Publication Date	Title	Journal
22860162	20111221	Detection of multiple sclerosis from exhaled breath using bilayers of polycyclic aromatic hydrocarbons and single-wall carbon nanotubes	ACS chemical neuroscience
21332135	20110316	Tetrathienoanthracene-based copolymers for efficient solar cells	Journal of the American Chemical Society
22347583	20110301	Isolation of a strain of Pseudomonas putida capable of metabolizing anionic detergent sodium dodecyl sulfate (SDS)	Iranian journal of microbiology
20380394	20100504	Chlorophyll-a derivatives with various hydrocarbon ester groups for efficient dye-sensitized solar cells: static and ultrafast evaluations on electron injection and charge collection processes	Langmuir : the ACS journal of surfaces and colloids

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GHS Hazard Statement:	H304 (100%): May be fatal if swallowed and enters airways [Danger Aspiration hazard]
Precautionary Statement:	P301+P316, P331, P405, and P501
Signal Word:	Danger

Complexity:	76.1
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	170.203450829
Formal Charge:	0
Heavy Atom Count:	12
Hydrogen Bond Acceptor Count:	0
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	170.203450829
Rotatable Bond Count:	8
Topological Polar Surface Area:	0Å²
Undefined Atom Stereocenter Count:	1
Undefined Bond Stereocenter Count:	0
XLogP3:	6.4