Propargyl-PEG4-acid - ≥98% , CAS No.1415800-32-6

CAS: 1415800-32-6 Cat. No.: P412744 Summenformel: C12H20O6 Molekulargewicht: 260.279 EG-Nummer: 853-600-7 PubChem CID: 77078488
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GRADE & PURITY ≥98%
Synonyms
Tetraoxahexadec-15-yn-1-oic acid | MFCD22683284 | AMY4485 | Propargyl-PEG4-COOH | Propyne-PEG3-CH2CH2COOH | 4,7,10,13-Tetraoxahexadec-15-yn-1-oic acid | 3-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]propanoic acid | 4,7,10,13-TETRAOXAHEXADEC-15-YNOIC ACID |
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
Application
227,228,229
★
Size
Deutschland (EU)
USA*
Price
Qty
100mg
P412744-100mg
—
6 Auf Lager
12,93€
250mg
P412744-250mg
—
7 Auf Lager
18,14€
1g
P412744-1g
—
4 Auf Lager
68,46€
5g
P412744-5g
—
2 Auf Lager
339,20€
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Product description

Propargyl-PEG4-acid is a PEG-based PROTAC linker can be used in the synthesis of BTK-IAP PROTACs Ibrutinib (HY-10997)-based PROTAC 2 and an analogue PROTAC 3. PROTAC 3 causes BTK degradation with a DC50 of 200 nM in THP-1 cells.

Specifications

Synonyme
Tetraoxahexadec-15-yn-1-oic acid | MFCD22683284 | AMY4485 | Propargyl-PEG4-COOH | Propyne-PEG3-CH2CH2COOH | 4,7,10,13-Tetraoxahexadec-15-yn-1-oic acid | 3-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]propanoic acid | 4,7,10,13-TETRAOXAHEXADEC-15-YNOIC ACID |
Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
Propargyl-PEG4-acid is a PEG-based PROTAC linker that is applicable to the synthesis of BTK-IAP PROTACs Ibrutinib-based PROTAC 2 and an analogue PROTAC 3. PROTAC 3 causes BTK degradation with DC50 of 200 nM in THP-1 cells.
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid488202373
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488202373
Kanonisches LächelnC#CCOCCOCCOCCOCCC(=O)O
IUPAC Name3-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]propanoic acid
InChIKeyWMBXAUWIPBFEOK-UHFFFAOYSA-N
INCHI1S/C12H20O6/c1-2-4-15-6-8-17-10-11-18-9-7-16-5-3-12(13)14/h1H,3-11H2,(H,13,14)
Isomere SMILES C#CCOCCOCCOCCOCCC(=O)O
PubChem CID 77078488
Molekulargewicht 260.279

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
SuperclassOrganic acids and derivatives
KlasseCarboxylic acids and derivatives
SubclassCarboxylic acids
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acids
Alternative Parents Monocarboxylic acids and derivatives  Dialkyl ethers  Acetylides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Acetylide - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

8 results found

Lot NumberCertificate TypeDatumArtikel
G2307674Certificate of AnalysisJun 08, 2023 P412744
G2307681Certificate of AnalysisJun 08, 2023 P412744
G2307682Certificate of AnalysisJun 08, 2023 P412744
G2307684Certificate of AnalysisJun 08, 2023 P412744
G2307686Certificate of AnalysisJun 08, 2023 P412744
G2307688Certificate of AnalysisJun 08, 2023 P412744
G2307689Certificate of AnalysisJun 08, 2023 P412744
G2307729Certificate of AnalysisJun 08, 2023 P412744
Chemische und physikalische Eigenschaften
LöslichkeitSolubility (25°C) In vitro      
Brechungsindex1.460
Molekulargewicht260.279 g/mol
XLogP3-0.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count13
Exact Mass260.126 Da
Monoisotopic Mass260.126 Da
Topological Polar Surface Area74.200 Ų
Heavy Atom Count18
Formal Charge0
Complexity244.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs und Artikel
Citations of This Product
Referenzen
1. Kun Chen, Guixin Wang, Xuedong Wang, Huili Wang.  (2023)  A smartphone-based ratiometric fluoroprobe based on blue-red dual-emission signals of thiochrome and copper nanoclusters for sensitive assay of metam-sodium in cucumbers.  TALANTA,      [PMID:37207510] [10.1016/j.talanta.2023.124673]
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