VBIT-4 - ≥99% , CAS No.2086257-77-2

CAS: 2086257-77-2 Cat. No.: V413014 Molecular Weight: 457.87 EC Number: 829-870-7 PubChem CID: 126697666
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
N-(4-chlorophenyl)-4-hydroxy-3-[4-[4-(trifluoromethoxy)phenyl]piperazin-1-yl]butanamide | SCHEMBL18641899 | Z2074895470 | EX-A5330 | N-(4-chlorophenyl)-4-hydroxy-3-{4-[4-(trifluoromethoxy)phenyl]piperazin-1-yl}butanamide | QYSQXVAEFPWMEM-UHFFFAOYSA-N | EN
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1mg
V413014-1mg
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5mg
V413014-5mg
4

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10mg
V413014-10mg
2

$583.90

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25mg
V413014-25mg
2

$1,201.90

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50mg
V413014-50mg
2

$1,922.90

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100mg
V413014-100mg
2

$3,364.90

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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

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

Overview

Information

VBIT-4 VBIT-4 is a voltage-dependent anion channel (VDAC) oligomerization inhibitor that decreases mitochondrial DNA (mtDNA) release, type I interferon (IFN) signaling, neutrophil extracellular traps, and disease severity in a mouse model of systemic lupus erythematosus.


Targets

VDAC ; mtDNA ; IFN

Specifications

Synonyms
N-(4-chlorophenyl)-4-hydroxy-3-[4-[4-(trifluoromethoxy)phenyl]piperazin-1-yl]butanamide | SCHEMBL18641899 | Z2074895470 | EX-A5330 | N-(4-chlorophenyl)-4-hydroxy-3-{4-[4-(trifluoromethoxy)phenyl]piperazin-1-yl}butanamide | QYSQXVAEFPWMEM-UHFFFAOYSA-N | EN
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
VBIT-4 is a voltage-dependent anion channel (VDAC) oligomerization inhibitor that decreases mitochondrial DNA (mtDNA) release, type I interferon (IFN) signaling, neutrophil extracellular traps, and disease severity in a mouse model of systemic lupus eryth
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Purity
≥99%
Names and Identifiers
Pubchem Sid504773017
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504773017
Canonical SmilesC1CN(CCN1C2=CC=C(C=C2)OC(F)(F)F)C(CC(=O)NC3=CC=C(C=C3)Cl)CO
IUPAC NameN-(4-chlorophenyl)-4-hydroxy-3-[4-[4-(trifluoromethoxy)phenyl]piperazin-1-yl]butanamide
InChIKeyQYSQXVAEFPWMEM-UHFFFAOYSA-N
INCHI1S/C21H23ClF3N3O3/c22-15-1-3-16(4-2-15)26-20(30)13-18(14-29)28-11-9-27(10-12-28)17-5-7-19(8-6-17)31-21(23,24)25/h1-8,18,29H,9-14H2,(H,26,30)
Isomeric SMILES C1CN(CCN1C2=CC=C(C=C2)OC(F)(F)F)C(CC(=O)NC3=CC=C(C=C3)Cl)CO
PubChem CID 126697666
Molecular Weight 457.87

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
SuperclassOrganoheterocyclic compounds
ClassDiazinanes
SubclassPiperazines
Intermediate Tree Nodes Not available
Direct ParentPhenylpiperazines
Alternative Parents N-arylpiperazines  Anilides  Phenoxy compounds  Phenol ethers  N-arylamides  Dialkylarylamines  Aniline and substituted anilines  N-alkylpiperazines  Chlorobenzenes  N-acyl amines  Trihalomethanes  Trialkylamines  Amino acids and derivatives  Vinyl chlorides  Enamines  Chloroalkenes  Carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organofluorides  Organochlorides  Organic oxides  Hydrocarbon derivatives  Alkyl fluorides  Alcohols and polyols  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents N-arylpiperazine - Phenylpiperazine - Anilide - Phenoxy compound - Aniline or substituted anilines - Dialkylarylamine - N-arylamide - Tertiary aliphatic/aromatic amine - Phenol ether - N-alkylpiperazine - Halobenzene - Chlorobenzene - Fatty acyl - Benzenoid - N-acyl-amine - Fatty amide - Monocyclic benzene moiety - Trihalomethane - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Amino acid or derivatives - Azacycle - Chloroalkene - Haloalkene - Vinyl halide - Vinyl chloride - Enamine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Halomethane - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organochloride - Organohalogen compound - Amine - Alkyl halide - Alkyl fluoride - Alcohol - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as phenylpiperazines. These are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

7 results found

Lot NumberCertificate TypeDateItem
I2216557Certificate of AnalysisJun 09, 2025 V413014
I2216558Certificate of AnalysisJun 09, 2025 V413014
I2216559Certificate of AnalysisJun 09, 2025 V413014
I2216561Certificate of AnalysisJun 09, 2025 V413014
I2216556Certificate of AnalysisJun 20, 2022 V413014
J2310487Certificate of AnalysisJun 20, 2022 V413014
K2328125Certificate of AnalysisJun 20, 2022 V413014
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 92 mg/mL (200.93 mM); Ethanol: 92 mg/mL (200.93 mM); Water: Insoluble;
Molecular Weight457.900 g/mol
XLogP33.900
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count8
Rotatable Bond Count7
Exact Mass457.138 Da
Monoisotopic Mass457.138 Da
Topological Polar Surface Area65.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity560.000
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
Citations of This Product
References
1. You Yi-ping, Yan Liang, Ke Hua-yu, Li Ya-ping, Shi Zi-jian, Zhou Zhi-ya, Yang Hai-yan, Yuan Tao, Gan Ying-qing, Lu Na, Xu Li-hui, Hu Bo, Ou-Yang Dong-yun, Zha Qing-bing, He Xian-hui.  (2024)  Baicalin inhibits PANoptosis by blocking mitochondrial Z-DNA formation and ZBP1-PANoptosome assembly in macrophages.  ACTA PHARMACOLOGICA SINICA,      [PMID:39223367] [10.1038/s41401-024-01376-8]
2. Jinpeng Lv, Huansha Zhang, Wenhao Yu, Peiwen Jiang, Chuanwei Yin, Wenhui Xu, Yan Cao, Rongyin Gao.  (2026)  Targeting VDAC1-dependent mtDNA release attenuates fibroblast innate immune activation and vitiligo pathogenesis.  INTERNATIONAL IMMUNOPHARMACOLOGY,      [PMID:41722540] [10.1016/j.intimp.2026.116411]
3. Lv Jinpeng, Xu Wenhui, Jiang Peiwen, Yu Wenhao, Xue Hui, Hu Nan, Cao Yan, Zhang Huansha, Yin Chuanwei, Gao Rongyin.  (2026)  Mitochondrial DNA release via VDAC1 in keratinocytes: a key driver of innate immunity and vitiligo pathogenesis.  Cell Death & Disease,      [PMID:] [10.1038/s41419-026-08585-5]
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