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Merck

T57401

Tridecane

≥99%

Synonym(s):

Cactus Normal Paraffin N 13, Cetiol iSAN, Paraffin N 13, n-Tridecane

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About This Item

Linear Formula:
CH3(CH2)11CH3
CAS Number:
629-50-5
Molecular Weight:
184.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24900311
EC Number:
211-093-4
Beilstein/REAXYS Number:
1733089
MDL number:
MFCD00008979
Assay:
≥99%

Key Documents

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InChI key

IIYFAKIEWZDVMP-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCCCC

vapor density

6.4 (vs air)

vapor pressure

1 mmHg ( 59.4 °C)

assay

≥99%

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.)

Quality Level

100

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Application

Tridecane can be used as a:
  • Reagent for the hydrodechlorination of 4‑chlorophenol in the presence of bimetallic nanocrystals as a catalyst.
  • Reactant to synthesize α, ω-dicarboxylic acids through terminal oxygenation in the presence of an inorganic-biohybrid catalyst.

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H304,H413

Hazard Classifications

Aquatic Chronic 4 - Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

174.2 °F

flash_point_c

79 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX5756
MKCW6785
MKCV4738
MKCS4909
MKCQ4764

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An unexpected mixture of substances in the defensive secretions of the tubuliferan thrips, Callococcithrips fuscipennis (Moulton)
Tschuch G, et al.
Journal of Chemical Ecology, 34(6), 742-747 (2008)
Chemical composition and biological activities of essential oil from the leaves of Sesuvium portulacastrum
Magwa ML, et al.
Journal of Ethnopharmacology, 103(1), 85-89 (2006)
Raúl A Laumann et al.
Journal of chemical ecology, 35(1), 8-19 (2009-01-08)
We tested the hypotheses that host-searching behavior of the egg parasitoids Telenomus podisi and Trissolcus basalis may be differentially influenced by the different blends of volatiles released from the metathoracic glands of adult stink bug host species. We further studied
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
Aurora J Cruz Cabeza et al.
Chemical communications (Cambridge, England), (16)(16), 1600-1602 (2007-05-29)
We report on experimental and theoretical evidence for solvent inclusion in form II carbamazepine (R3) and discuss the implications for the formation and stability of this form.
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