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1,4-dihydroxy-2-naphthoic acid - ≥98% , CAS No.31519-22-9

CAS: 31519-22-9 Cat. No.: D137175 Peso molecular: 204.18 Beilstein Registry Number: 10442 Número EC: 250-674-7
COA
1,4-dihydroxy-2-naphthoic acid - ≥98% CAS No(31519-22-9) by Aladdin Scientific
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
InChI=1/C11H8O4/c12-9-5-8(11(14)15)10(13)7-4-2-1-3-6(7)9/h1-5,12-13H,(H,14,15) | STL513558 | (HYDROXYPROPYL)METHYLCELLULOSE | 1,4-Dihydroxy-2-naphthoicAcid | CHEBI:18094 | HMS3741M11 | D2296 | W-106893 | SY014338 | 1,4-dihydroxy-2-naphthoate | 1U77MR5Q7O
Storage
Room temperature
Shipped In
Normal
★
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D137175-1g
5
20,90US$
5g
D137175-5g
4
41,90US$
25g
D137175-25g
1
111,90US$
Enter a quantity for the sizes you want to add.
Bulk / Custom
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Descripción general Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Calculadoras de soluciones Reseñas
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

1,4-Dihydroxy-2-naphthoic acid from Propionibacterium freudenreichii is known to promote the proliferation of Bifidobacterium. It has potential therapeutic application for psoriasis treatment

Specifications

Sinónimos
InChI=1/C11H8O4/c12-9-5-8(11(14)15)10(13)7-4-2-1-3-6(7)9/h1-5, 12-13H, (H, 14, 15) | STL513558 | (HYDROXYPROPYL)METHYLCELLULOSE | 1, 4-Dihydroxy-2-naphthoicAcid | CHEBI:18094 | HMS3741M11 | D2296 | W-106893 | SY014338 | 1, 4-dihydroxy-2-naphthoate | 1U77MR5Q7O
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Tipo de acción
ACTIVATOR
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488179538
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179538
Sonrisas canónicasC1=CC=C2C(=C1)C(=CC(=C2O)C(=O)O)O
IUPAC Name1,4-dihydroxynaphthalene-2-carboxylic acid
InChIKeyVOJUXHHACRXLTD-UHFFFAOYSA-N
INCHI1S/C11H8O4/c12-9-5-8(11(14)15)10(13)7-4-2-1-3-6(7)9/h1-5,12-13H,(H,14,15)
Isómeros SMILES C1=CC=C2C(=C1)C(=CC(=C2O)C(=O)O)O
WGK Alemania 3
CAS alternativo 31519-22-9
Términos de entrada MeSH 1,4-dihydroxy-2-naphthoate;1,4-dihydroxy-2-naphthoic acid
Peso molecular 204.18
Beilstein 10442
Reaxy-Rn 2111226
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2111226&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseNaphthalenes
SubclassNaphthalenecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentNaphthalenecarboxylic acids
Alternative Parents Naphthols and derivatives  Salicylic acid and derivatives  Hydroquinones  1-hydroxy-2-unsubstituted benzenoids  Vinylogous acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 2-naphthalenecarboxylic acid - Dihydroxybenzoic acid - 1-naphthol - Hydroxybenzoic acid - Salicylic acid or derivatives - Hydroquinone - 1-hydroxy-2-unsubstituted benzenoid - Vinylogous acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as naphthalenecarboxylic acids. These are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors naphthalenediols - dihydroxy monocarboxylic acid - naphthoic acid
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

13 results found

Lot NumberCertificate TypeFechaArticulo
B2219385Certificate of AnalysisSep 09, 2025 D137175
B2219390Certificate of AnalysisSep 09, 2025 D137175
G2326659Certificate of AnalysisAug 14, 2023 D137175
G2326674Certificate of AnalysisAug 10, 2023 D137175
G2326663Certificate of AnalysisAug 10, 2023 D137175
G2326665Certificate of AnalysisAug 10, 2023 D137175
G2326656Certificate of AnalysisAug 10, 2023 D137175
G2326616Certificate of AnalysisAug 10, 2023 D137175
G2326670Certificate of AnalysisAug 10, 2023 D137175
D23061086Certificate of AnalysisApr 11, 2023 D137175
B2219391Certificate of AnalysisJan 13, 2022 D137175
A2212403Certificate of AnalysisDec 29, 2021 D137175
A2212407Certificate of AnalysisDec 29, 2021 D137175

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Propiedades químicas y físicas
SolubilidadSlightly soluble in water.
Punto de fusión (°C)191 °C(dec.)
Peso molecular204.180 g/mol
XLogP32.500
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass204.042 Da
Monoisotopic Mass204.042 Da
Topological Polar Surface Area77.800 Ų
Heavy Atom Count15
Formal Charge0
Complexity253.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
Reseñas

Reseñas de cliente

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