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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:
26825-89-8
Molecular Weight:
349.35
MDL number:
MFCD00040769
UNSPSC Code:
12352100
PubChem Substance ID:
329760910
NACRES:
NA.22

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

Related Categories

Application

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

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

684511-1G:
684511-5G:
684511-VAR:
684511-BULK:

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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