Hydrochinon - ≥99%(HPLC) , CAS No.123-31-9

Name: Hydrochinon - ≥99%(HPLC) , CAS No.123-31-9
Brand: Aladdin Scientific
SKU: H108947
Availability: InStock

CAS: 123-31-9 Cat. No.: H108947 Summenformel: C₆H₆O₂ Molekulargewicht: 110.11 Beilstein Registry Number: 605970 EG-Nummer: 204-617-8

683 Citations COA

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Hydrochinon - ≥99%(HPLC) CAS No(123-31-9) by Aladdin Scientific

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QUALITÄT & REINHEIT ≥99%(HPLC)

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≥99%(HPLC) für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Literaturbeleg

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

Übersicht

Hydrochinon ist eine phenolische Verbindung, die natürlich in Kaffee, Tee und Wein vorkommt. Sie wird in der fotografischen, chemischen und kosmetischen Industrie verwendet. Hydrochinon wird als Mittel zur Hautaufhellung verwendet. Es wird topisch angewendet, um Melisma, Sommersprossen und senile Lentigines zu behandeln. Hydrochinon wird mit exogener Ochronose, Dermatitis und Hautreizungen in Verbindung gebracht. Es hemmt die Melanogenese.

Ein kleines Chinon-Molekül mit Wirksamkeit als topisches Präparat.

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≥99%(HPLC)

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Reinheit

≥99%(HPLC)

Namen und Kennungen

Pubchem Sid

508813318

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=

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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

3D-Struktur

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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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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TYR Tclin Tyrosinase (717 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CXCL8 Tchem Interleukin-8 (642 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA3 Tclin Carbonic anhydrase III (753 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA6 Tclin Carbonic anhydrase VI (993 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

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AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ARSA Tbio Cerebroside-sulfatase (655 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5B Tclin Carbonic anhydrase VB (957 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MTOR Tclin Serine/threonine-protein kinase mTOR (13850 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HL-60 (67320 Activities)

Lot Number	Certificate Type	Datum	Artikel
J2609435	Certificate of Analysis	Sep 21, 2026	H108947
J2609436	Certificate of Analysis	Sep 21, 2026	H108947
J2609856	Certificate of Analysis	Sep 21, 2026	H108947
J2609857	Certificate of Analysis	Sep 21, 2026	H108947
J2623484	Certificate of Analysis	Sep 21, 2026	H108947
J2623464	Certificate of Analysis	Sep 21, 2026	H108947
J2623463	Certificate of Analysis	Sep 21, 2026	H108947
I2617999	Certificate of Analysis	Sep 14, 2026	H108947
I2617987	Certificate of Analysis	Sep 14, 2026	H108947
I2617986	Certificate of Analysis	Sep 14, 2026	H108947
B2321879	Certificate of Analysis	Jul 30, 2026	H108947
G2629555	Certificate of Analysis	Jul 14, 2026	H108947
G2629558	Certificate of Analysis	Jul 14, 2026	H108947
G2629556	Certificate of Analysis	Jul 14, 2026	H108947
G2629552	Certificate of Analysis	Jul 14, 2026	H108947
G2629544	Certificate of Analysis	Jul 14, 2026	H108947
B2609020	Certificate of Analysis	Feb 03, 2026	H108947
D2601419	Certificate of Analysis	Feb 03, 2026	H108947
D2601417	Certificate of Analysis	Feb 03, 2026	H108947
D2601418	Certificate of Analysis	Feb 03, 2026	H108947
B2606174	Certificate of Analysis	Feb 03, 2026	H108947
B2602201	Certificate of Analysis	Feb 03, 2026	H108947
D2601420	Certificate of Analysis	Feb 03, 2026	H108947
B2606175	Certificate of Analysis	Jan 09, 2026	H108947
B2603424	Certificate of Analysis	Jan 09, 2026	H108947
B2603388	Certificate of Analysis	Jan 09, 2026	H108947
B2603384	Certificate of Analysis	Jan 09, 2026	H108947
A2621278	Certificate of Analysis	Jan 09, 2026	H108947
A2613169	Certificate of Analysis	Jan 09, 2026	H108947
A2613162	Certificate of Analysis	Jan 09, 2026	H108947
L2525139	Certificate of Analysis	Jan 06, 2026	H108947
A2203066	Certificate of Analysis	Jun 09, 2025	H108947
F2503357	Certificate of Analysis	May 20, 2025	H108947
F2503354	Certificate of Analysis	May 20, 2025	H108947
F2503355	Certificate of Analysis	May 20, 2025	H108947
F2503353	Certificate of Analysis	May 20, 2025	H108947
L2523052	Certificate of Analysis	Apr 03, 2025	H108947
D2517436	Certificate of Analysis	Apr 03, 2025	H108947
D2517418	Certificate of Analysis	Apr 03, 2025	H108947
D2517417	Certificate of Analysis	Apr 03, 2025	H108947
D2517416	Certificate of Analysis	Apr 03, 2025	H108947
D2517415	Certificate of Analysis	Apr 03, 2025	H108947
G2123348	Certificate of Analysis	Jan 16, 2025	H108947
L2411670	Certificate of Analysis	Nov 30, 2024	H108947
L2411685	Certificate of Analysis	Nov 30, 2024	H108947
L2411686	Certificate of Analysis	Nov 30, 2024	H108947
G2403496	Certificate of Analysis	Jun 22, 2024	H108947
G2403497	Certificate of Analysis	Jun 22, 2024	H108947
D2410443	Certificate of Analysis	Mar 22, 2024	H108947
D2410444	Certificate of Analysis	Mar 22, 2024	H108947
D2410282	Certificate of Analysis	Mar 22, 2024	H108947
D2410283	Certificate of Analysis	Mar 22, 2024	H108947
D2410281	Certificate of Analysis	Mar 22, 2024	H108947
C2409147	Certificate of Analysis	Feb 29, 2024	H108947
C2409148	Certificate of Analysis	Feb 29, 2024	H108947
C2409149	Certificate of Analysis	Feb 29, 2024	H108947
A2203077	Certificate of Analysis	Oct 07, 2023	H108947
L2115642	Certificate of Analysis	Sep 20, 2023	H108947
L2115643	Certificate of Analysis	Sep 20, 2023	H108947
J2310144	Certificate of Analysis	Jul 29, 2023	H108947
J2310145	Certificate of Analysis	Jul 29, 2023	H108947
H2312302	Certificate of Analysis	Jul 29, 2023	H108947
H2312296	Certificate of Analysis	Jul 29, 2023	H108947
H2312289	Certificate of Analysis	Jul 29, 2023	H108947
H2312288	Certificate of Analysis	Jul 29, 2023	H108947
B2321906	Certificate of Analysis	Nov 17, 2022	H108947
B2321887	Certificate of Analysis	Nov 17, 2022	H108947
B2321860	Certificate of Analysis	Nov 17, 2022	H108947
H2231560	Certificate of Analysis	Jul 29, 2022	H108947
H2231559	Certificate of Analysis	Jul 29, 2022	H108947
H2231520	Certificate of Analysis	Jul 29, 2022	H108947
H2231519	Certificate of Analysis	Jul 29, 2022	H108947
E2224183	Certificate of Analysis	Mar 12, 2022	H108947
E2224159	Certificate of Analysis	Mar 12, 2022	H108947
E2224182	Certificate of Analysis	Mar 12, 2022	H108947

Löslichkeit	A quinone small molecule with efficacy as a topical preparation.
Empfindlichkeit	Light and air sensitive.
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

Hydrochinon - ≥99%(HPLC) , CAS No.123-31-9

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