18-Crown-6 - ≥99% , CAS No.17455-13-9

CAS: 17455-13-9 Cat. No.: C105797 분자식: C12H24O6 분자량: 264.32 EC 번호: 241-473-5
주문 가능
GRADE & PURITY ≥99%
Synonyms
1,4,7,10,13,16-Hexaoxacyclooctadecane | Hexaoxacyclo-octadecane | 18-Crown 6-ether
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
★
Size
USA
독일 (EU)*
Price
Qty
5g
C105797-5g
9 재고 있음
—
US$9.90
10g
C105797-10g
2 재고 있음
—

US$10.90

US$16.90
저장 US$6.00 (35.50%)
25g
C105797-25g
3 재고 있음
—
US$14.90
100g
C105797-100g
1 재고 있음
—
US$39.90
500g
C105797-500g
2 재고 있음
—

US$92.90

US$139.90
저장 US$47.00 (33.60%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

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

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 124 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

동의어
1,4,7,10,13,16-Hexaoxacyclooctadecane | Hexaoxacyclo-octadecane | 18-Crown 6-ether
사양 및 순도
≥99%
보관 조건
Store at 2-8°C,Argon charged
배송
Wet ice
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순수함
≥99%
이름과 식별자
Pubchem Sid
정식 스마일
C1COCCOCCOCCOCCOCCO1
IUPAC Name
1,4,7,10,13,16-hexaoxacyclooctadecane
InChIKey
XEZNGIUYQVAUSS-UHFFFAOYSA-N
INCHI
1S/C12H24O6/c1-2-14-5-6-16-9-10-18-12-11-17-8-7-15-4-3-13-1/h1-12H2
이성체 SMILES
C1COCCOCCOCCOCCOCCO1
WGK 독일
3
RTECS
MP4500000
분자량
264.32
Reaxy-Rn
1619616
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1619616&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
SuperclassOrganic oxygen compounds
분류Organooxygen compounds
SubclassEthers
Intermediate Tree Nodes Not available
Direct ParentDialkyl ethers
Alternative Parents Oxacyclic compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oxacycle - Organoheterocyclic compound - Dialkyl ether - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
설명This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
External Descriptors saturated organic heteromonocyclic parent - crown ether
3D 구조
상호 작용 화학 구조 모델





관련 대상(인간)
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MIA PaCa-2 (5949 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
관련 대상(비인간)
Ttr Transthyretin (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gallus gallus (1187 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
작용 메커니즘
인증서(CoA, COO, BSE/TSE 및 분석 차트)
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.

54 results found

Lot NumberCertificate Type날짜항목
K2219406Certificate of AnalysisSep 04, 2026 C105797
F2625269Certificate of AnalysisJun 12, 2026 C105797
F2625475Certificate of AnalysisJun 12, 2026 C105797
F2625530Certificate of AnalysisJun 12, 2026 C105797
F2625533Certificate of AnalysisJun 12, 2026 C105797
L2510265Certificate of AnalysisNov 13, 2025 C105797
K2524300Certificate of AnalysisNov 13, 2025 C105797
K2524302Certificate of AnalysisNov 13, 2025 C105797
K2524309Certificate of AnalysisNov 13, 2025 C105797
K2524310Certificate of AnalysisNov 13, 2025 C105797
K2524311Certificate of AnalysisNov 13, 2025 C105797
L2510256Certificate of AnalysisNov 13, 2025 C105797
L2510257Certificate of AnalysisNov 13, 2025 C105797
L2510264Certificate of AnalysisNov 13, 2025 C105797
E2507288Certificate of AnalysisApr 21, 2025 C105797
E2507289Certificate of AnalysisApr 21, 2025 C105797
E2507290Certificate of AnalysisApr 21, 2025 C105797
E2507291Certificate of AnalysisApr 21, 2025 C105797
D2511353Certificate of AnalysisJul 18, 2024 C105797
D2511351Certificate of AnalysisJul 18, 2024 C105797
D2511364Certificate of AnalysisJul 18, 2024 C105797
D2511375Certificate of AnalysisJul 18, 2024 C105797
I2413384Certificate of AnalysisMay 30, 2024 C105797
I2413383Certificate of AnalysisMay 30, 2024 C105797
I2413382Certificate of AnalysisMay 30, 2024 C105797
I2413381Certificate of AnalysisMay 30, 2024 C105797
I2413380Certificate of AnalysisMay 30, 2024 C105797
H2408318Certificate of AnalysisMar 30, 2024 C105797
H2412335Certificate of AnalysisMar 30, 2024 C105797
H2412337Certificate of AnalysisMar 30, 2024 C105797
F2427008Certificate of AnalysisNov 20, 2023 C105797
L2304126Certificate of AnalysisNov 20, 2023 C105797
L2304141Certificate of AnalysisNov 20, 2023 C105797
L2304142Certificate of AnalysisNov 20, 2023 C105797
L2304143Certificate of AnalysisNov 20, 2023 C105797
F2312061Certificate of AnalysisMay 27, 2023 C105797
F2312047Certificate of AnalysisMay 27, 2023 C105797
F2312049Certificate of AnalysisMay 27, 2023 C105797
F2312054Certificate of AnalysisMay 27, 2023 C105797
H2511037Certificate of AnalysisMay 27, 2023 C105797
F2312055Certificate of AnalysisMay 27, 2023 C105797
F2312057Certificate of AnalysisMay 27, 2023 C105797
E2309471Certificate of AnalysisApr 23, 2023 C105797
E2309462Certificate of AnalysisApr 23, 2023 C105797
E2308343Certificate of AnalysisApr 23, 2023 C105797
E2306469Certificate of AnalysisApr 23, 2023 C105797
K2219407Certificate of AnalysisSep 07, 2022 C105797
K2219408Certificate of AnalysisSep 07, 2022 C105797
K2219409Certificate of AnalysisSep 07, 2022 C105797
K2219404Certificate of AnalysisSep 07, 2022 C105797
G2216450Certificate of AnalysisJun 18, 2022 C105797
G2216449Certificate of AnalysisJun 18, 2022 C105797
G2216448Certificate of AnalysisJun 18, 2022 C105797
G2216446Certificate of AnalysisJun 18, 2022 C105797
화학 및 물리적 특성
용해성Solubility in Methanol almost transparency;Soluble in water.
감도Heat and Moisture Sensitive
발화점(°F)>235.4 °F
발화점(°C)>113 °C
끓는점(°C)190°C/0.7mmHg
녹는점(°C)38-41°C
분자량264.310 g/mol
XLogP3-0.700
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count0
Exact Mass264.157 Da
Monoisotopic Mass264.157 Da
Topological Polar Surface Area55.400 Ų
Heavy Atom Count18
Formal Charge0
Complexity108.000
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
자주 묻는 질문과 기사
Tert-Butyl peroxybenzoate, TBPB
Structural–Functional Analysis of the Methoxy Group (–OCH₃) in Approved Small-Molecule Drugs: Mechanisms, Evidence Chains, and Product-Selection Navigation (with Related Product Tables)
Experimental Selection Logic for Phase-Transfer Catalysts: Choosing Catalysts by Phase-State System, Source of Anionic Species, and Reaction Task
Why Small Molecules Can Also Serve as Catalysts: Judging Organocatalytic Systems from Reaction Objectives and Activatable Structural Sites
Synthesis Strategy of Pentafluorothio Group - Synthesis of Aliphatic Compounds Containing SF₅
Overcoming the Electronic-Effect Limitations of Nucleophilic Aromatic Substitution in Fluoroarenes: Anion Activation, Concerted Substitution, and HF Capture by t-Bu-P4
How to Bypass α-Fluoride Elimination: Bromine-Transfer Capture and Oxidative Coupling of α,α-Difluorobenzylic Anions
Selectivity Mechanism of the Triple Aryne–Tetrazine Cascade Reaction: Reaction-Pathway Switching and Intermediate Transformations
Supramolecular Materials: From Molecular Recognition and Self-Assembly to Dynamic Function
Citations of This Product
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