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184241

Sigma-Aldrich

4-Butoxybenzyl alcohol

98%

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About This Item

Linear Formula:
CH3(CH2)3OC6H4CH2OH
CAS Number:
Molecular Weight:
180.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

form

solid

refractive index

n20/D 1.518 (lit.)

mp

29-32 °C (lit.)

SMILES string

CCCCOc1ccc(CO)cc1

InChI

1S/C11H16O2/c1-2-3-8-13-11-6-4-10(9-12)5-7-11/h4-7,12H,2-3,8-9H2,1H3

InChI key

MGKNBDBZIKPUFM-UHFFFAOYSA-N

Application

4-Butoxybenzyl alcohol was used in the synthesis of:
  • 3-(4-butoxyphenyl)-1-phenylpropan-1-ol
  • 3-(4-butoxyphenyl)-1-phenylpropan-1-one
  • 4-butoxybenzyl chloride

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Dinakar Gnanamgari et al.
Organic & biomolecular chemistry, 6(23), 4442-4445 (2008-11-14)
Primary alcohols can be coupled with secondary benzylic alcohols by an air-stable catalytic system involving terpyridine ruthenium or iridium complexes.
Molecular recognition directed self-assembly of tubular liquid crystalline and crystalline supramolecular architectures from taper shaped (15-crown-5) methyl 3, 4, 5-tris (p-alkyloxybenzyloxy) benzoates and (15-crown-5) methyl 3, 4, 5-tris (p-dodecyloxy) benzoate.
Johansson G, et al.
Journal of the Chemical Society. Perkin Transactions 1, 4, 447-459 (1994)

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