Skip to Content
Merck
CN

464503

2-Decyl-1-tetradecanol

97%

Synonym(s):

2-Decyl-1-tetradecanol, 2-Decylmyristyl alcohol, 2-Decyltetradecanol, 2-Decyltetradecyl alcohol, 2-Dodecyl-1-dodecanol, Decyltetradecanol, Decyltetradecyl alcohol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
CH3(CH2)11CH[(CH2)9CH3]CH2OH
CAS Number:
58670-89-6
Molecular Weight:
354.65
NACRES:
NA.22
PubChem Substance ID:
24870189
UNSPSC Code:
12352100
EC Number:
261-385-0
MDL number:
MFCD00674096
Assay:
97%

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2-Decyl-1-tetradecanol, 97%

InChI key

CAYHVMBQBLYQMT-UHFFFAOYSA-N

InChI

1S/C24H50O/c1-3-5-7-9-11-13-14-16-18-20-22-24(23-25)21-19-17-15-12-10-8-6-4-2/h24-25H,3-23H2,1-2H3

SMILES string

CCCCCCCCCCCCC(CO)CCCCCCCCCC

assay

97%

refractive index

n20/D 1.457 (lit.)

bp

271-275 °C/33 mmHg (lit.)

mp

17-20 °C (lit.)

density

0.842 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

100

Related Categories

Application

2-Decyl-1-tetradecanol may be used in the preparation of 2-decyltetradecyl (4-nitrophenyl)[11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl]phosphonate.

General description

2-Decyl-1-tetradecanol participates in the preparation of monosaccharide glycolipid.

Storage Class

10 - Combustible liquids

wgk

nwg

flash_point_f

410.0 °F - open cup

flash_point_c

210 °C - open cup

ppe

Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCT9066
MKCK1350
MKCG7197
MKCG3701
MKBX5250V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H J Deussen et al.
Bioorganic & medicinal chemistry letters, 10(17), 2027-2031 (2000-09-15)
The design, synthesis, and inhibition properties of two new triglyceride analogue biotinylated suicide inhibitors (2) and (3) for directed molecular evolution of lipolytic enzymes by phage-display is described.
Specific surface modification of the acetylene-linked glycolipid vesicle by click chemistry.
Ito H, et al.
Chemical Communications (Cambridge, England), 48(45), 5650-5652 (2012)
Andrea Garcia-Ortiz et al.
ChemSusChem, 13(4), 707-714 (2020-01-09)
Biomass-derived surfactants with very good surface tension and critical micellar concentration properties were obtained by conversion of methyl levulinate into methyl 4-alkoxypentanoates through reductive etherification with aliphatic alcohols. Among different bifunctional acid/metal catalysts best results were obtained with Pd on

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service