21604

2-Bromohexadecanoic acid

≥99.0% (GC)

Manufacturer: Sigma Aldrich

CAS Number: 18263-25-7

Synonym(S): 2-Bromopalmitic acid

Select a Size

Pack Size SKU Availability Price
1 G 21604-1-G In Stock ₹ 5,760.00

21604 - 1 G

₹ 5,760.00

In Stock

Quantity

1

Base Price: ₹ 5,760.00

GST (18%): ₹ 1,036.80

Total Price: ₹ 6,796.80

Assay

≥99.0% (GC)

form

solid

mp

52-54 °C

solubility

methanol: soluble 1 g/10 mL, clear, colorlesschloroform: solubleethanol: solublewater: insoluble

SMILES string

CCCCCCCCCCCCCCC(Br)C(O)=O

InChI

1S/C16H31BrO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15H,2-14H2,1H3,(H,18,19)

InChI key

DPRAYRYQQAXQPE-UHFFFAOYSA-N

Gene Information

human ... PPARD(5467)

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Description

  • Application: <ul><li><strong>Chemo-immunotherapy Applications:</strong> 2-Bromohexadecanoic acid has been utilized to create bioactive fatty acid analog-derived hybrid nanoparticles for chemo-immunotherapy against carcinoma, demonstrating potential in cancer treatment without the need for antibodies (Tan et al., 2023).</li><li><strong>Drug Target Identification for Coronavirus:</strong> 2-bromopalmitate (2-BP) can be used as an inhibitor and is used to suppressed SADS-CoV treatment (Luo et al., 2021).</li><li><strong>Cancer Therapy Enhancement:</strong> This compound has shown efficacy in sensitizing osteosarcoma cells to adriamycin-induced apoptosis through modulation of CHOP, indicating its therapeutic potential in enhancing cancer treatment (Xu et al., 2019).</li><li><strong>Membrane Protein Localization in Sertoli Cells: </strong>It has been involved in studies related to the localization of the androgen receptor to plasma membranes by binding to caveolin-1 in mouse Sertoli cells, contributing to the understanding of cellular signaling pathways. It is Used to inhibit palmitoylation of androgen receptor (AR) and used to evaluate the effect of the inhibitor on androgen receptor (AR) translocation (Deng et al., 2017).</li><li><strong>Palmitoylation Inhibition:</strong> 2-Bromohexadecanoic acid has been profiled as an irreversible inhibitor of palmitoylation, providing insights into the regulation of protein modifications and their implications in various diseases (Davda et al., 2013).</li></ul>

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

235.4 °F

Flash Point(C)

113 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Show Difference

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Sigma Aldrich

21604

≥99.0% (GC)...


Assay:
≥99.0% (GC)

form:
solid

mp:
52-54 °C

solubility:
methanol: soluble 1 g/10 mL, clear, colorlesschloroform: solubleethanol: solublewater: insoluble

SMILES string:
CCCCCCCCCCCCCCC(Br)C(O)=O

InChI:
1S/C16H31BrO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15H,2-14H2,1H3,(H,18,19)

InChI key:
DPRAYRYQQAXQPE-UHFFFAOYSA-N

Gene Information:
human ... PPARD(5467)

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Sigma Aldrich

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Assay:
≥99.0%

form:
powder, crystals or chunks

mp:
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solubility:
__

SMILES string:
__

InChI:
__

InChI key:
__

Gene Information:
__

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Sigma Aldrich

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SMILES string:
N#CS[Co]SC#N

InChI:
1S/2CHNS.Co/c2*2-1-3;/h2*3H;/q;;+2/p-2

InChI key:
INDBQWVYFLTCFF-UHFFFAOYSA-L

Gene Information:
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Assay:
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SMILES string:
COC1=CCC=CC1

InChI:
1S/C7H10O/c1-8-7-5-3-2-4-6-7/h2-3,6H,4-5H2,1H3

InChI key:
RGXIXVNKYUAKHS-UHFFFAOYSA-N

Gene Information:
__