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464503

2-Decyl-1-tetradecanol

Name: 2-Decyl-1-tetradecanol
Brand: ALDRICH

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

Quality Level

100

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.)

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

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Organic Building Blocks

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.

WGK

nwg

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Design and synthesis of triglyceride analogue biotinylated suicide inhibitors for directed molecular evolution of lipolytic enzymes.

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)

Transforming Methyl Levulinate into Biosurfactants and Biolubricants by Chemoselective Reductive Etherification with Fatty Alcohols.

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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