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16860

Sigma-Aldrich

2-Bromodecanoic acid

≥96.0% (AT)

Synonym(s):

2-Bromocapric acid

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About This Item

Linear Formula:
CH3(CH2)7CHBrCOOH
CAS Number:
2623-95-2
Molecular Weight:
251.16
Beilstein:
1767667
EC Number:
220-086-5
MDL number:
MFCD00014335
UNSPSC Code:
12352100
PubChem Substance ID:
57647592

Assay

≥96.0% (AT)

refractive index

n20/D 1.471

bp

116-118 °C/0.05 mmHg (lit.)

density

1.21 g/mL at 20 °C (lit.)

SMILES string

CCCCCCCCC(Br)C(O)=O

InChI

1S/C10H19BrO2/c1-2-3-4-5-6-7-8-9(11)10(12)13/h9H,2-8H2,1H3,(H,12,13)

InChI key

KNLOTZNPRIFUAR-UHFFFAOYSA-N

Application

2-Bromodecanoic acid was used as extractant in synergistic solvent extraction of trivalent actinides (Am and Cm) and some lanthanides. It was used in the synthesis of 2-bromodecanoic acid benzhydryl ester.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

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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Synergistic solvent extraction of trivalent americium and europium by 2-bromodecanoic acid and neutral nitrogen-containing reagents.
Hagstrom I, et al.
Solvent Extr. Ion Exch., 17(2), 221-242 (1999)
André Fontes et al.
Nuclear medicine and biology, 38(3), 363-370 (2011-04-16)
In this work, we report on a synthetic strategy using amphiphilic DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid)-based chelators bearing a variable-sized α-alkyl chain at one of the pendant acetate arms (from 6 to 14 carbon atoms), compatible with their covalent coupling to amine-bearing

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