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464503

Sigma-Aldrich

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

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About This Item

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

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

SMILES string

CCCCCCCCCCCCC(CO)CCCCCCCCCC

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

InChI key

CAYHVMBQBLYQMT-UHFFFAOYSA-N

Related Categories

General description

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

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.

Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point(F)

410.0 °F - open cup

Flash Point(C)

210 °C - open cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT9066
MKCK1350
MKCG7197
MKCG3701
MKBX5250V

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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

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