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6-Hydroxy-1-tetralone - >98.0%, high purity , CAS No.3470-50-6

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6-Hydroxy-1-tetralone - >98.0%, high purity , CAS No.3470-50-6

2 Citations

COA

Grade & Purity:

≥98%

Cas Number: 3470-50-6
Molecular Weight: 162.19
MDL number: MFCD00156670
PubChem CID: 4679494
PubChem SID: 488194957

In stock

Item Number

H156890

Grouped product items
SKU	Size	Availability	Price
H156890-1g	1g	3	$16.90
H156890-5g	5g	3	$62.90
H156890-10g	10g	2	$112.90
H156890-25g	25g	4	$213.90
H156890-100g	100g	3	$769.90
H156890-500g	500g	1	$3,462.90

View related series

ketone (798) Non heterocyclic block (8163)

Basic Description

Synonyms	AM20040236 \| FT-0648908 \| MB00784 \| 6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone \| 6-hydroxy tetralone \| AKOS005258189 \| J-019722 \| BDBM50017515 \| STL555185 \| Z877546758 \| DTXSID30405488 \| 6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone, 98% \| AC-1123 \| EN300-5885
Specifications & Purity	≥98%
Shipped In	Normal
Product Description	6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone (6-Hydroxy-1-tetralone) can be prepared by the demethylation of 6-methoxy-3,4-dihydro-1(2H)-naphthalenone. It participates in the synthesis of 2-alkylamino-6-hydroxy-5-hydroxymethyl-1,2,3,4-tetrahydro-1-naphthalenols. Its pKa value has been reported to be 7.74. 6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone (6-Hydroxy-1-tetralone) may be used in the synthesis of: . 5-chloromethyl-6-hydroxy-3,4-dihydro-1(2H)-naphthalenone. . 6-(4-(3-(piperidin-1-yl)propoxy)benzyloxy)-1-tetralone. . 6-(3-(piperidin-1-yl)propoxy)-1-tetralone.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Tetralins

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Tetralins
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Tetralins
Alternative Parents	Aryl alkyl ketones 1-hydroxy-2-unsubstituted benzenoids Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Tetralin - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.
External Descriptors	Not available
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

Associated Targets(Human)

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

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

MAOB Tclin Monoamine oxidase B (8835 Activities)

Discover Target: MAOB

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

PRKCI Tchem Protein kinase C iota (2821 Activities)

Discover Target: PRKCI

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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488194957
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488194957
IUPAC Name	6-hydroxy-3,4-dihydro-2H-naphthalen-1-one
INCHI	InChI=1S/C10H10O2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h4-6,11H,1-3H2
InChIKey	FNSQPQKPPGALFA-UHFFFAOYSA-N
Smiles	C1CC2=C(C=CC(=C2)O)C(=O)C1
Isomeric SMILES	C1CC2=C(C=CC(=C2)O)C(=O)C1
WGK Germany	3
Molecular Weight	162.19
Reaxy-Rn	2043992
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2043992&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

14 results found

Lot Number	Certificate Type	Date	Item
E2528443	Certificate of Analysis	Jul 23, 2024	H156890
D2501668	Certificate of Analysis	Jun 24, 2024	H156890
J2414446	Certificate of Analysis	Jun 24, 2024	H156890
J2414447	Certificate of Analysis	Jun 24, 2024	H156890
H1920091	Certificate of Analysis	Jun 06, 2023	H156890
G2321088	Certificate of Analysis	Mar 11, 2022	H156890
E2223169	Certificate of Analysis	Mar 11, 2022	H156890
E2223167	Certificate of Analysis	Mar 11, 2022	H156890
E2223166	Certificate of Analysis	Mar 11, 2022	H156890
A2214230	Certificate of Analysis	Jan 27, 2022	H156890
C1823073	Certificate of Analysis	Jan 19, 2022	H156890
G2321101	Certificate of Analysis	Jan 19, 2022	H156890
C1823074	Certificate of Analysis	Jan 19, 2022	H156890
G2225035	Certificate of Analysis	Aug 09, 2021	H156890

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Chemical and Physical Properties

Melt Point(°C)	155 °C
Molecular Weight	162.180 g/mol
XLogP3	1.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	162.068 Da
Monoisotopic Mass	162.068 Da
Topological Polar Surface Area	37.300 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	188.000
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

How to Cite Aladdin Scientific Products?

1. Yaqiong Zhang, Xu Xu, Lei Zhang. (2023) Capsulation of red emission chromophore into the CoZn ZIF as nanozymes for on-site visual cascade detection of phosphate ions, o-phenylenediamine, and benzaldehyde. SCIENCE OF THE TOTAL ENVIRONMENT, 856 (159091).
2. Longbin Xu, Xu He, Pinyi Ma, Xin Liu, Fangmei Zhang, Ying Sun, Daqian Song, Xinghua Wang. (2018) A water-soluble fluorescent probe for the sensitive detection of endogenous alkaline phosphatase in living cells. DYES AND PIGMENTS, 159 (584).

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