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Merck
CN

269239

Tridecanal

technical grade, 90%

Synonym(s):

Tridecyl aldehyde

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About This Item

Linear Formula:
CH3(CH2)11CHO
CAS Number:
10486-19-8
Molecular Weight:
198.34
NACRES:
NA.22
PubChem Substance ID:
24856319
UNSPSC Code:
12352100
EC Number:
234-004-0
MDL number:
MFCD00007018

Key Documents

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Product Name

Tridecanal, technical grade, 90%

InChI key

BGEHHAVMRVXCGR-UHFFFAOYSA-N

InChI

1S/C13H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h13H,2-12H2,1H3

SMILES string

CCCCCCCCCCCCC=O

grade

technical grade

assay

90%

form

liquid

refractive index

n20/D 1.438 (lit.)

bp

132-136 °C/8 mmHg (lit.)

density

0.835 g/mL at 25 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

Quality Level

100

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Application

Tridecanal was used as a model compound in the development of nonradioactive assays for the enzymes 2-hydroxyacyl-CoA lyase (HACL1) and sphingosine-1-phosphate lyase (SGPL1) employing the Hantzsch reaction.

General description

The uptake of NO(3) on solid tridecanal was studied.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBQ0579
SHBN1346
MKCC6237
MKCB9020
MKCB1953V

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Richard Iannone et al.
Physical chemistry chemical physics : PCCP, 13(21), 10214-10223 (2011-04-22)
We report the first measurements of the reactive uptake of NO(3) with condensed-phase aldehydes. Specifically, we studied NO(3) uptake on solid tridecanal and the uptake on liquid binary mixtures containing tridecanal and saturated organic molecules (diethyl sebacate, dioctyl sebacate, and
Serena Mezzar et al.
Journal of lipid research, 55(3), 573-582 (2013-12-11)
Long-chain aldehydes are commonly produced in various processes, such as peroxisomal α-oxidation of long-chain 3-methyl-branched and 2-hydroxy fatty acids and microsomal breakdown of phosphorylated sphingoid bases. The enzymes involved in the aldehyde-generating steps of these processes are 2-hydroxyacyl-CoA lyase (HACL1)
Karolina Wieszczycka et al.
Photochemistry and photobiology, 91(4), 786-796 (2015-03-13)
The goal of the research was to study the reactivity of the hydrophobic 2- and 3-pyridineketoximes under exposure to UV-VIS light. The photodegradation was conducted in both toluene and heptane for 10 h under atmosphere of argon. Ten-hour irradiation experiments demonstrated

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