Vanillin - for synthesis , CAS No.121-33-5

Name: Vanillin - for synthesis , CAS No.121-33-5
Brand: Aladdin Scientific
SKU: V431597
Availability: InStock

CAS: 121-33-5 Cat. No.: V431597 Summenformel: C₈H₈O₃ Molekulargewicht: 152.15 Beilstein Registry Number: 472792 EG-Nummer: 204-465-2 PubChem CID: 1183

430 Citations COA

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QUALITÄT & REINHEIT for Synthesis ?

Synonyms

4-Hydroxy-3-methoxybenzaldehyde

Storage

Protected from light,Room temperature,Argon charged

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Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen Häufig gestellte Fragen

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Warum diese Qualität

for synthesis zur Synthese für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Protected from light,Room temperature,Argon charged Versand Normal. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 430 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Spezifikationen

Synonyme

4-Hydroxy-3-methoxybenzaldehyde

Spezifikationen & Reinheit

for synthesis

Storage

Protected from light,Room temperature,Argon charged

Verschickt in

Normal

Note

zur Synthese

Namen und Kennungen

Pubchem Sid

504750476

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504750476

Kanonisches Lächeln

COC1=C(C=CC(=C1)C=O)O

IUPAC Name

4-hydroxy-3-methoxybenzaldehyde

InChIKey

MWOOGOJBHIARFG-UHFFFAOYSA-N

INCHI

1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3

Isomere SMILES

COC1=C(C=CC(=C1)C=O)O

WGK Deutschland

RTECS

YW5775000

PubChem CID

1183

Molekulargewicht

152.15

Beilstein

472792

Dokumentation

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<<<<<<< HEAD SDS herunterladen → ======= SDS herunterladen → >>>>>>> release248-p3

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Klasse Phenols
    - Subclass Methoxyphenols

Kingdom	Organic compounds
Superclass	Benzenoids
Klasse	Phenols
Subclass	Methoxyphenols
Intermediate Tree Nodes	Not available
Direct Parent	Methoxyphenols
Alternative Parents	Hydroxybenzaldehydes Phenoxy compounds Methoxybenzenes Benzoyl derivatives Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Methoxyphenol - Hydroxybenzaldehyde - Anisole - Benzaldehyde - Benzoyl - Phenoxy compound - Phenol ether - Methoxybenzene - Alkyl aryl ether - Aryl-aldehyde - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Ether - Organooxygen compound - Aldehyde - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
External Descriptors	a small molecule
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. DOI: 10.1186/s13321-016-0174-y

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TRIM33 Tchem E3 ubiquitin-protein ligase TRIM33 (2 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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SLC6A1 Tclin GABA transporter 1 (308 Activities)

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ABAT Tclin Gamma-amino-N-butyrate transaminase (140 Activities)

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CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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ALDH5A1 Tclin Succinate semialdehyde dehydrogenase (19 Activities)

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PRKDC Tchem DNA-dependent protein kinase (1929 Activities)

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MPO Tchem Myeloperoxidase (1002 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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K562 (73714 Activities)

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KM12 (47707 Activities)

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M14 (47487 Activities)

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MCF7 (126967 Activities)

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OVCAR-3 (48710 Activities)

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OVCAR-4 (44535 Activities)

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OVCAR-5 (45555 Activities)

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OVCAR-8 (47708 Activities)

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PANC-1 (6144 Activities)

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PC-3 (62116 Activities)

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RPMI-8226 (44974 Activities)

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SF-295 (48000 Activities)

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SH-SY5Y (11521 Activities)

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SK-MEL-28 (48833 Activities)

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SK-MEL-5 (47095 Activities)

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SN12C (47755 Activities)

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SNB-19 (46794 Activities)

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TK-10 (45540 Activities)

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U-251 (51189 Activities)

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UACC-257 (46019 Activities)

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UO-31 (46270 Activities)

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786-0 (47912 Activities)

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A549 (127892 Activities)

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NCI/ADR-RES (33767 Activities)

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T47D (39041 Activities)

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EKVX (44102 Activities)

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NCI-H322M (45589 Activities)

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H9 (1832 Activities)

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HCC 2998 (41480 Activities)

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Htr7 Serotonin 7 (5-HT7) receptor (19 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Faah Anandamide amidohydrolase (3907 Activities)

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Artemia salina (1320 Activities)

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Mycobacterium tuberculosis (203094 Activities)

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Candida albicans (78123 Activities)

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Nakaseomyces glabratus (9108 Activities)

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Candida tropicalis (8381 Activities)

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Meloidogyne incognita (862 Activities)

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Musca domestica (713 Activities)

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Mus musculus (284745 Activities)

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Human immunodeficiency virus 1 (70413 Activities)

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RAW264.7 (28094 Activities)

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RBL-2H3 (1162 Activities)

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Vero (26788 Activities)

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Rdl GABA receptor subunit (76 Activities)

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Fusarium verticillioides (912 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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BCHE Cholinesterase (8742 Activities)

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Curvularia lunata (722 Activities)

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Fusarium incarnatum (10 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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PNLIP Pancreatic triacylglycerol lipase (476 Activities)

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Trypanosoma congolense (178 Activities)

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Wirkungsmechanismen

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

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12 results found

Lot Number	Certificate Type	Datum	Artikel
F2612419	Certificate of Analysis	Jun 24, 2026	V431597
E2609045	Certificate of Analysis	May 20, 2026	V431597
J2612028	Certificate of Analysis	May 20, 2026	V431597
L2525591	Certificate of Analysis	Dec 31, 2025	V431597
L2525593	Certificate of Analysis	Dec 31, 2025	V431597
C2519650	Certificate of Analysis	Mar 25, 2025	V431597
J2428282	Certificate of Analysis	Nov 02, 2024	V431597
G2419017	Certificate of Analysis	Jul 26, 2024	V431597
D23061287	Certificate of Analysis	Apr 19, 2023	V431597
C2425092	Certificate of Analysis	Apr 15, 2023	V431597
D23061285	Certificate of Analysis	Apr 15, 2023	V431597
L2326023	Certificate of Analysis	Apr 15, 2023	V431597

Chemische und physikalische Eigenschaften

Löslichkeit	9g/L
Empfindlichkeit	Light sensitive；Air and moisture sensitive
Flammpunkt (°F)	307°F
Flammpunkt (°C)	153°C
Siedepunkt (°C)	170 °C/15 mmHg
Schmelzpunkt (°C)	81-83°C
Molekulargewicht	152.150 g/mol
XLogP3	1.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	2
Exact Mass	152.047 Da
Monoisotopic Mass	152.047 Da
Topological Polar Surface Area	46.500 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	135.000
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

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How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What does for synthesis mean?

for synthesis indicates that the material has been processed and tested for specialty industrial processing. Specifications focus on the impurities that affect performance in that application — for example, metal content for electronics, particle size for batteries, refractive index for optics, or moisture content for moisture-sensitive processes.

How should this product be stored?

Store at room temperature, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 121-33-5, the molecular formula is C8H8O3, and the molecular weight is 152.15 g/mol. InChIKey MWOOGOJBHIARFG-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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Vanillin - for synthesis , CAS No.121-33-5

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Vanillin - for synthesis , CAS No.121-33-5

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