Hydroquinone - for synthesis , CAS No.123-31-9

Name: Hydroquinone - for synthesis , CAS No.123-31-9
Brand: Aladdin Scientific
SKU: H431621
Availability: InStock

CAS: 123-31-9 Cat. No.: H431621 Summenformel: C₆H₆O₂ Molekulargewicht: 110.11 Beilstein Registry Number: 605970 EG-Nummer: 204-617-8

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Literaturbeleg

In 683 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

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Synonyme

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for synthesis

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Namen und Kennungen

Pubchem Sid

504750416

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504750416

Kanonisches Lächeln

C1=CC(=CC=C1O)O

IUPAC Name

benzene-1,4-diol

InChIKey

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

INCHI

1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H

Isomere SMILES

C1=CC(=CC=C1O)O

WGK Deutschland

RTECS

MX3500000

UN-Nummer

3077

Verpackungsgruppe

III

Molekulargewicht

110.11

Beilstein

605970

Reaxy-Rn

605970

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605970&ln=

Dokumentation

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Taxonomic Classification

Taxonomy Tree

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

Kingdom	Organic compounds
Superclass	Benzenoids
Klasse	Phenols
Subclass	Benzenediols
Intermediate Tree Nodes	Not available
Direct Parent	Hydroquinones
Alternative Parents	1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Organooxygen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Hydroquinone - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as hydroquinones. These are compounds containing a hydroquinone moiety, which consists of a benzene ring with a hydroxyl groups at positions 1 and 4.
External Descriptors	an electron-transfer-related quinol - a benzenediol
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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CA2 Tclin Carbonic anhydrase 2 (2 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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TYR Tclin Tyrosinase (717 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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CXCL8 Tchem Interleukin-8 (642 Activities)

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CA3 Tclin Carbonic anhydrase III (753 Activities)

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CA6 Tclin Carbonic anhydrase VI (993 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

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ARSA Tbio Cerebroside-sulfatase (655 Activities)

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CA5B Tclin Carbonic anhydrase VB (957 Activities)

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CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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CA14 Tclin Carbonic anhydrase XIV (1305 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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MTOR Tclin Serine/threonine-protein kinase mTOR (13850 Activities)

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NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)

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HBB Tbio Hemoglobin beta chain (329 Activities)

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ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

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CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)

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CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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HL-60 (67320 Activities)

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K562 (73714 Activities)

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SH-SY5Y (11521 Activities)

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U-251 (51189 Activities)

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U-87 MG (3946 Activities)

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A549 (127892 Activities)

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HEK293 (82097 Activities)

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KB (17409 Activities)

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Lymphoblastoid cell (5959 Activities)

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FEN1 Tchem Flap endonuclease 1 (12055 Activities)

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HIF1A Tchem Hypoxia-inducible factor 1 alpha (6027 Activities)

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SIRT1 Tchem NAD-dependent deacetylase sirtuin 1 (3505 Activities)

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HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

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LMNA Tbio Prelamin-A/C (36751 Activities)

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RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)

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BLM Tchem Bloom syndrome protein (4248 Activities)

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HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

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THPO Tbio Thrombopoietin (834 Activities)

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Ca7 Carbonic anhydrase VII (3 Activities)

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polC DNA polymerase III (243 Activities)

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Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

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Ca13 Carbonic anhydrase XIII (322 Activities)

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CA4 Carbonic anhydrase IV (1713 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Carbonic anhydrase (69 Activities)

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Artemia salina (1320 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Porphyromonas gingivalis (651 Activities)

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Micrococcus luteus (7463 Activities)

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Escherichia coli (133304 Activities)

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Streptococcus mutans (2687 Activities)

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Bacillus subtilis (32866 Activities)

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Plasmodium falciparum (966862 Activities)

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Candida albicans (78123 Activities)

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Trypanosoma cruzi (99888 Activities)

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Cavia porcellus (23802 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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L1210 (27553 Activities)

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P388 (20296 Activities)

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J774 (3120 Activities)

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lef Anthrax lethal factor (7585 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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pfk 6-phospho-1-fructokinase (7870 Activities)

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Ca15 Carbonic anhydrase 15 (173 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

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Danio rerio (3092 Activities)

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Gambusia affinis (76 Activities)

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Trichophyton mentagrophytes (4846 Activities)

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Large T antigen (1457 Activities)

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Mapt Microtubule-associated protein tau (6 Activities)

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

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

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nfo Endonuclease 4 (425 Activities)

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Melan-a (81 Activities)

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Anopheles gambiae (126 Activities)

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Wirkungsmechanismen

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

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18 results found

Lot Number	Certificate Type	Datum	Artikel
G2511381	Certificate of Analysis	Jun 24, 2025	H431621
G2511380	Certificate of Analysis	Jun 24, 2025	H431621
G2511343	Certificate of Analysis	Jun 24, 2025	H431621
C2623187	Certificate of Analysis	Jun 24, 2025	H431621
F2608176	Certificate of Analysis	Jun 24, 2025	H431621
D2518473	Certificate of Analysis	Apr 22, 2025	H431621
D2518472	Certificate of Analysis	Apr 22, 2025	H431621
D2518471	Certificate of Analysis	Apr 22, 2025	H431621
D2410445	Certificate of Analysis	Apr 20, 2024	H431621
J2409022	Certificate of Analysis	Apr 20, 2024	H431621
A2506270	Certificate of Analysis	Apr 20, 2024	H431621
D2410444	Certificate of Analysis	Apr 20, 2024	H431621
D2410443	Certificate of Analysis	Apr 20, 2024	H431621
D2410442	Certificate of Analysis	Apr 20, 2024	H431621
C2324065	Certificate of Analysis	Mar 13, 2023	H431621
C2324063	Certificate of Analysis	Mar 13, 2023	H431621
C2324062	Certificate of Analysis	Mar 13, 2023	H431621
C2324061	Certificate of Analysis	Mar 13, 2023	H431621

Chemische und physikalische Eigenschaften

Löslichkeit	70g/L
Flammpunkt (°C)	165℃
Siedepunkt (°C)	285-287°C
Schmelzpunkt (°C)	170-171°C
Molekulargewicht	110.110 g/mol
XLogP3	0.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	110.037 Da
Monoisotopic Mass	110.037 Da
Topological Polar Surface Area	40.500 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	54.900
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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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.

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Store at room temperature.

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This product is classified as dangerous goods and ships via FedEx DG Service. Ground and other economy services are not available, and delivery to some destinations or address types may be restricted.

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

The CAS Number is 123-31-9, the molecular formula is C6H6O2, and the molecular weight is 110.11 g/mol. InChIKey QIGBRXMKCJKVMJ-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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Hydroquinone - for synthesis , CAS No.123-31-9

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Hydroquinone - for synthesis , CAS No.123-31-9

Lagerung & Versand

Qualitätsdokumente

Literaturbeleg

Spezifikationen

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

✅ Analysezertifikat (COA)

📊 Datenblatt

🔬 Spezifikationsblatt

Erweiterte Daten

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

Häufig gestellte Fragen

📚 Zitationen nach Anwendung

Benötigen Sie Hilfe bei der Auswahl der Qualität?

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