Butyl Phenyl Ether - ≥99%(GC) , CAS No.1126-79-0

CAS: 1126-79-0 Cat. No.: B153006 Peso molecular: 150.22 Beilstein Registry Number: 6143 Número EC: 214-426-1
Disponible para pedir
GRADE & PURITY ≥99%(GC)
Synonyms
NSC 8467 | 4-06-00-00558 (Beilstein Handbook Reference) | EINECS 214-426-1 | BRN 1635559 | n-Butoxybenzene | AS-81526 | B0927 | WLN: 4OR | H804A5426K | NSC8467 | NSC-8467 | 1-Phenoxybutane | J-002817 | AKOS002710507 | Butoxybenzene | butoxy-benzene | n-Bu
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5ml
B153006-5ml
5
12,90US$
25ml
B153006-25ml
4
48,90US$
100ml
B153006-100ml
1
121,90US$
500ml
B153006-500ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
431,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Butyl phenyl ether was used as model compound to study the transformation of human pharmaceuticals detected in water during chlorine disinfection. It was used in the synthesis of amino acids with aryl-keto function in their side-chains.

Specifications

Sinónimos
NSC 8467 | 4-06-00-00558 (Beilstein Handbook Reference) | EINECS 214-426-1 | BRN 1635559 | n-Butoxybenzene | AS-81526 | B0927 | WLN: 4OR | H804A5426K | NSC8467 | NSC-8467 | 1-Phenoxybutane | J-002817 | AKOS002710507 | Butoxybenzene | butoxy-benzene | n-Bu
Especificaciones y pureza
≥99%(GC)
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%(GC)
Nombres e identificadores
Pubchem Sid488181974
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181974
Sonrisas canónicasCCCCOC1=CC=CC=C1
IUPAC Namebutoxybenzene
InChIKeyYFNONBGXNFCTMM-UHFFFAOYSA-N
INCHI1S/C10H14O/c1-2-3-9-11-10-7-5-4-6-8-10/h4-8H,2-3,9H2,1H3
Isómeros SMILES CCCCOC1=CC=CC=C1
WGK Alemania 2
RTECS KN5300000
Peso molecular 150.22
Beilstein 6143
Reaxy-Rn 1635559
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1635559&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
SuperclassBenzenoids
ClasePhenol ethers
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPhenol ethers
Alternative Parents Phenoxy compounds  Alkyl aryl ethers  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

9 results found

Lot NumberCertificate TypeFechaArticulo
D2418534Certificate of AnalysisMar 29, 2024 B153006
D2424179Certificate of AnalysisMar 20, 2024 B153006
D2424180Certificate of AnalysisMar 20, 2024 B153006
C2330305Certificate of AnalysisFeb 13, 2023 B153006
E1905012Certificate of AnalysisFeb 13, 2023 B153006
E2330148Certificate of AnalysisFeb 13, 2023 B153006
E2330153Certificate of AnalysisFeb 13, 2023 B153006
F2329272Certificate of AnalysisFeb 13, 2023 B153006
B2224134Certificate of AnalysisFeb 26, 2022 B153006
Propiedades químicas y físicas
Índice de refracción1.49
Punto de inflamación (°F)179 °F
Punto de inflamación (°C)82℃
Punto de ebullición (°C)210-211℃
Punto de fusión (°C)-19℃
Peso molecular150.220 g/mol
XLogP33.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count4
Exact Mass150.104 Da
Monoisotopic Mass150.104 Da
Topological Polar Surface Area9.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity84.900
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
Citations of This Product
Referencias
1. Yuanlong Guo, Gu Guo, Pengcheng Liu, Yang You, Jili Yuan, Gang Hu, Lei Dai, Michael North, Haibo Xie, Qiang Zheng.  (2023)  The synthesis of multifunctional cellulose graft alternating copolymers of 3,4-dihydrocoumarin and epoxides in DBU/DMSO/CO2 solvent system.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:37648137] [10.1016/j.ijbiomac.2023.126584]
2. Pengcheng Liu, Yuanlong Guo, Gu Guo, Lei Dai, Gang Hu, Haibo Xie.  (2023)  Lignin-grafting alternative copolymer of 3,4-dihydrocoumarin and epoxides as an active and flexible ingredient in sunscreen.  GREEN CHEMISTRY,  25  (11): (4469-4481).  [PMID:] [10.1039/D3GC00531C]
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