2-Bromohexadecanoic acid - Moligand™, ≥97% , CAS No.18263-25-7

CAS: 18263-25-7 Cat. No.: B135567 分子式: CH3(CH2)13CH(Br)CO2H 分子量: 335.32 Beilstein Registry Number: 1726517 EC番号: 242-137-0
注文可能
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥97%
Synonyms
CAS-18263-25-7 | CHEBI:133152 | NCGC00164251-02 | PD165437 | FT-0611564 | SCHEMBL97565 | LMFA01090011 | Spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one, 3',6'-dihydroxy-2',4',5',7'-tetraiodo-, disodium salt, monohydrate | 2-Bromohexadecanoic acid, purum,
Storage
Room temperature,Desiccated
Shipped In
Normal
Size
USA
ドイツ (EU)*
Price
Qty
1g
B135567-1g
4 在庫あり
$14.90
5g
B135567-5g
1 在庫あり
$49.90
25g
B135567-25g
3 在庫あり
$164.90
100g
B135567-100g
受注生産 · 8~12週間
$539.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™, ≥97% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

概要

2-Bromohexadecanoic acid (2-Bromopalmitate; 2-BP) is a palmitoylation inhibitor targeting DHHC (Asp-His-His-Cys) protein palmitoyltransferase. 2-Bromohexadecanoic acid inhibits palmitoylation of GSDME-C during pyroptosis and inhibits BAK/BAX-Caspase 3-GSDME pathway-mediated pyroptosis.

Specifications

同義語
CAS-18263-25-7 | CHEBI:133152 | NCGC00164251-02 | PD165437 | FT-0611564 | SCHEMBL97565 | LMFA01090011 | Spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one, 3',6'-dihydroxy-2',4',5',7'-tetraiodo-, disodium salt, monohydrate | 2-Bromohexadecanoic acid, purum,
仕様と純度
Moligand™, ≥97%
保管条件
Room temperature,Desiccated
入荷
Normal
等級
Moligand™
アクションタイプ
INHIBITOR
純度
≥97%
名前と識別子
パブケム・シド488186058
パブケム・シド・ウルhttps://pubchem.ncbi.nlm.nih.gov/substance/488186058
カノニカル・スマイルCCCCCCCCCCCCCCC(C(=O)O)Br
IUPAC Name2-bromohexadecanoic acid
InChIKeyDPRAYRYQQAXQPE-UHFFFAOYSA-N
INCHI1S/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)
異性体SMILES CCCCCCCCCCCCCCC(C(=O)O)Br
WGKドイツ 3
分子量 335.32
Beilstein 1726517
Reaxy-Rn 1726517
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1726517&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
分類Fatty Acyls
SubclassFatty acids and conjugates
Intermediate Tree Nodes Not available
Direct ParentLong-chain fatty acids
Alternative Parents Halogenated fatty acids  Alpha-halocarboxylic acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organobromides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl bromides  
Molecular FrameworkAliphatic acyclic compounds
Substituents Long-chain fatty acid - Halogenated fatty acid - Alpha-halocarboxylic acid - Alpha-halocarboxylic acid or derivatives - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organobromide - Organohalogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Alkyl bromide - Alkyl halide - Organooxygen compound - Hydrocarbon derivative - Aliphatic acyclic compound
説明This compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
External Descriptors Halogenated fatty acids
3 D構造
インタラクティブ化学構造モデル





関連ターゲット(人間)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ZDHHC20 Tbio Palmitoyltransferase ZDHHC20 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
関連ターゲット(非人間)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
作用メカニズム
証明書(CoA、COO、BSE/TSEと分析図)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

17 results found

Lot NumberCertificate Type日付商品
E2608251Certificate of AnalysisApr 18, 2026 B135567
E2608252Certificate of AnalysisApr 18, 2026 B135567
E2608253Certificate of AnalysisApr 18, 2026 B135567
E2608254Certificate of AnalysisApr 18, 2026 B135567
D2603013Certificate of AnalysisApr 15, 2026 B135567
A2425113Certificate of AnalysisOct 29, 2025 B135567
H2508020Certificate of AnalysisAug 18, 2025 B135567
I2509051Certificate of AnalysisAug 18, 2025 B135567
L2210261Certificate of AnalysisSep 19, 2024 B135567
L2210247Certificate of AnalysisSep 19, 2024 B135567
L2210229Certificate of AnalysisSep 19, 2024 B135567
L2210228Certificate of AnalysisSep 19, 2024 B135567
I2227040Certificate of AnalysisJul 17, 2024 B135567
L2210236Certificate of AnalysisNov 09, 2022 B135567
D2403042Certificate of AnalysisNov 09, 2022 B135567
I2227068Certificate of AnalysisOct 10, 2022 B135567
I2227067Certificate of AnalysisOct 10, 2022 B135567

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化学的性質と物理的性質
引火点(°F)235.4 °F
引火点(°C)113 °C
融点(°C)52-54°C
分子量335.320 g/mol
XLogP37.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count14
Exact Mass334.151 Da
Monoisotopic Mass334.151 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count19
Formal Charge0
Complexity207.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
よくある質問と記事
Citations of This Product
参考文献
1. Yun Zhou, Song Yue, Lihua Li, Jiahua Zhang, Lei Chen, Jun Chen.  (2024)  SMPDL3B is palmitoylated and stabilized by ZDHHC5, and its silencing aggravates diabetic retinopathy of db/db mice: Activation of NLRP3/NF-κB pathway.  CELLULAR SIGNALLING,      [PMID:38266744] [10.1016/j.cellsig.2024.111064]
2. Fang Liu, Yaru Li, Yao Li, Zheng Wang, Xin Li, Yancheng Liu, Yanjun Zhao.  (2024)  Triggering multiple modalities of cell death via dual-responsive nanomedicines to address the narrow therapeutic window of β-lapachone.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:39270391] [10.1016/j.jcis.2024.09.063]
3. You Xujun, Li Honghan, Li Qixin, Zhang Qing, Cao Yiguo, Fu Wei, Wang Bin.  (2025)  Astragaloside IV-PESV facilitates pyroptosis by enhancing palmitoylation of GSDMD protein mediated by ZDHHC1.  NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,      [PMID:40237800] [10.1007/s00210-025-04122-x]
4. Xiaoli Su, Xingli Tan, Ying Wang, Weiwei Liang, Di Wang, Di Huo, Hongyong Wang, Yan Qi, Wenmo Zhang, Ling Han, Dongmei Zhang, Ming Wang, Jing Xu, Shuyu Wang, Jing Wang, Honglin Feng.  (2026)  COMMD1 Induces Copper Deficiency of SOD1 by Inhibiting the Palmitoylation of CCS in ALS.  JOURNAL OF NEUROSCIENCE,      [PMID:42156174] [10.1523/JNEUROSCI.1803-25.2026]
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