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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock 2,6-Dimethyl-4-hydroxybenzaldehyde - ≥97% , CAS No.70547-87-4
Synonyms
AC-1194 | Benzaldehyde, 4-hydroxy-2,6-dimethyl- | AKOS005145852 | FT-0654331 | AM20041052 | Z1201617288 | CTABR | SCHEMBL516188 | Klorocid S | EN300-301908 | Q-200486 | 2.6-dimethyl-4-hydroxy-benzaldehyde | 2,6-dimethyl-4-hydroxy benzaldehyde | 3,5-Dimeth
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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.
Specifications Synonymes
AC-1194 | Benzaldehyde, 4-hydroxy-2,6-dimethyl- | AKOS005145852 | FT-0654331 | AM20041052 | Z1201617288 | CTABR | SCHEMBL516188 | Klorocid S | EN300-301908 | Q-200486 | 2.6-dimethyl-4-hydroxy-benzaldehyde | 2,6-dimethyl-4-hydroxy benzaldehyde | 3,5-Dimeth
Spécifications et pureté
≥97%
Conditions de stockage de stockage
Room temperature
Noms et identifiants Pubchem Sid 508807812 Sourires canoniques CC1=CC(=CC(=C1C=O)C)O IUPAC Name 4-hydroxy-2,6-dimethylbenzaldehyde InChIKey XXTRGLCPRZQPHJ-UHFFFAOYSA-N INCHI 1S/C9H10O2/c1-6-3-8(11)4-7(2)9(6)5-10/h3-5,11H,1-2H3 Isomères SMILES CC1=CC(=CC(=C1C=O)C)O Poids moléculaire 150.18 Reaxy-Rn 1937522 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1937522&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 Kingdom Organic compounds Superclass Organic oxygen compounds Classe Organooxygen compounds Subclass Carbonyl compounds Intermediate Tree Nodes Aldehydes - Aryl-aldehydes - Benzaldehydes Direct Parent Hydroxybenzaldehydes Alternative Parents m-Xylenes Meta cresols Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Hydroxybenzaldehyde - M-xylene - Xylene - M-cresol - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Structure 3D Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Poids moléculaire 150.170 g/mol XLogP3 0.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 1 Exact Mass 150.068 Da Monoisotopic Mass 150.068 Da Topological Polar Surface Area 37.300 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 132.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Citations of This Product Références 1. Jinkang Dou, Lijie Cheng, Bojun Tan, Binghui Duan, Minghui Xu, Bozhou Wang, Ning Liu. (2023) Efficient metal-free crosslinking of common propellant binders using nitrile oxide–alkene click ligation. Polymer Chemistry, 14 (46): (5125-5132). [PMID: [10.1039/D3PY01081C ] 2. Jinkang Dou, Minghui Xu, Bojun Tan, Hongchang Mo, Xianming Lu, Bozhou Wang, Ning Liu. (2023) Synthesis of Highly Stable and Reactive Nitrile N-Oxides and Their Application as Catalyst-Free Crosslinkers. MACROMOLECULES, [PMID: [10.1021/acs.macromol.3c00360 ] 3. Qiushuang Zhang, Jinkang Dou, Minghui Xu, Bojun Tan, Hongchang Mo, Xianming Lu, Jianquan Wang, Ning Liu. (2024) Highly Flexible Polyether for Solid Propellants: Synthesis, Room Temperature Curing, Thermal Analysis, and Mechanical Properties. ACS Applied Polymer Materials, [PMID: [10.1021/acsapm.4c01709 ]
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