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Merck
CN

442713

Tridecane

analytical standard

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About This Item

Linear Formula:
CH3(CH2)11CH3
CAS Number:
629-50-5
Molecular Weight:
184.36
Beilstein:
1733089
EC Number:
211-093-4
MDL number:
MFCD00008979
UNSPSC Code:
23151816
PubChem Substance ID:
24867979

Key Documents

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grade

analytical standard

vapor density

6.4 (vs air)

vapor pressure

1 mmHg ( 59.4 °C)

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.425 (lit.)

bp

110-112 °C/12 mmHg (lit.)
234 °C (lit.)

mp

−6-−4 °C (lit.)

density

0.756 g/mL at 25 °C (lit.)

application(s)

environmental
petroleum

format

neat

storage temp.

room temp

SMILES string

CCCCCCCCCCCCC

InChI

1S/C13H28/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3-13H2,1-2H3

InChI key

IIYFAKIEWZDVMP-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Product 442713 has been discontinued. Product 91490 may be an acceptable replacement.

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H304,H413

Hazard Classifications

Aquatic Chronic 4 - Asp. Tox. 1

Supplementary Hazards

EUH066

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

174.2 °F

Flash Point(C)

79 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LC27047V
LC17793V
LC17616V
LC17560V
LC15298V

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Bo Li et al.
Chemical communications (Cambridge, England), 49(12), 1187-1189 (2013-01-04)
A phytochemical investigation of the cone of Pseudolarix amabilis led to the isolation of pseudolarenone (), a structurally novel pentacyclic (5/11/5/6/5) nortriterpenoid lactone with an unprecedented carbon skeleton featuring a unique bicyclo[8.2.1]tridecane core. Its structure and absolute configurations were elucidated
Jörg P Hehn et al.
Organic letters, 13(7), 1892-1895 (2011-03-09)
Starting from tetronate 1 (R = CH(2)OH), a short photochemical access to the 3,12-dioxatricyclo[8.2.1.0(6,13)]tridecane-skeleton 2 of briarellin and asbestinin diterpenes has been explored. In the course of these studies, a number of surprising observations were made. For example, a two-step
Dorit Eliyahu et al.
Journal of chemical ecology, 38(11), 1358-1365 (2012-10-20)
One characteristic of true bugs (Heteroptera) is the presence of dorsal abdominal glands in the immature nymphal stages. These glands usually produce defensive chemicals (allomones) that vary among taxa but are still similar in closely related groups. Knowledge of the
I V Ulezlo et al.
Prikladnaia biokhimiia i mikrobiologiia, 40(5), 533-535 (2004-11-24)
Yeast cultures belonging to the genera Candida, Torulopsis, Saccharomyces, Debaryomyces, Hansenula, Pichia, and Yarrowia, capable of synthesizing brassylic and sebacic fatty acids, were screened. Overall, about 200 cultures grown in media containing decane or tridecane as a sole source of
Anil Kumar Mishra et al.
Journal of drug targeting, 12(9-10), 559-567 (2004-12-29)
The purpose of this study was to obtain the convenient, synthetically useful bifunctional chelating agent, 6-(4-isothiocyanatobenzyl)-5,7-dioxo-1,11-(carboxymethyl)-1,4,8,11-tetraazacyclotridecane, and to apply it to stable (99m)Tc-labelling of monoclonal antibodies (mAbs). The chelate was synthesised by reaction of nitrobenzyl malonate and triethylenetetramine followed by
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