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Key Documents

684511

Sigma-Aldrich

Methyl 16-bromohexadecanoate

97%

Synonym(s):

16-bromohexadecanoic acid, methyl ester

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About This Item

Empirical Formula (Hill Notation):
C17H33BrO2
CAS Number:
Molecular Weight:
349.35
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

30-34 °C

SMILES string

COC(=O)CCCCCCCCCCCCCCCBr

InChI

1S/C17H33BrO2/c1-20-17(19)15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18/h2-16H2,1H3

InChI key

ZYTQDEJMRYPSHE-UHFFFAOYSA-N

Application

Omega-functionalized long chain protected carboxylic acid. Utility: building block for self-assembled monolayer molecules.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>230.0 °F - closed cup

Flash Point(C)

> 110 °C - closed cup

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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Mukesh K Pandey et al.
Nuclear medicine and biology, 80-81, 13-23 (2019-11-24)
The objectives of the present work were to optimize and validate the synthesis and stability of 14(R,S)-[18F]fluoro-6-thia-heptadecanoic acid ([18F]FTHA) and 16-[18F]fluoro-4-thia-palmitic acid ([18F]FTP) under cGMP conditions for clinical applications. Benzyl-14-(R,S)-tosyloxy-6-thiaheptadecanoate and methyl 16-bromo-4-thia-palmitate were used as precursors for the synthesis
Shane Pawsey et al.
Journal of the American Chemical Society, 125(14), 4174-4184 (2003-04-03)
The structures formed by the adsorption of carboxyalkylphosphonic acids on metal oxides were investigated by (1)H fast magic angle spinning (MAS), heteronuclear correlation (HETCOR), and (1)H double-quantum (DQ) MAS solid-state NMR experiments. The diacids HO(2)C(CH(2))(n)PO(3)H(2) (n = 2, 3, 11

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