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Merck
CN

41774

1,4-Dimethoxynaphthalene

fluorescent marker, ≥99.5% (HPLC)

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About This Item

Empirical Formula (Hill Notation):
C12H12O2
CAS Number:
10075-62-4
Molecular Weight:
188.22
EC Number:
233-209-2
UNSPSC Code:
12352200
PubChem Substance ID:
57650089
Beilstein/REAXYS Number:
2048082
MDL number:
MFCD00052378

Key Documents

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Product Name

1,4-Dimethoxynaphthalene, fluorescent marker, ≥99.5% (HPLC)

InChI key

FWWRTYBQQDXLDD-UHFFFAOYSA-N

InChI

1S/C12H12O2/c1-13-11-7-8-12(14-2)10-6-4-3-5-9(10)11/h3-8H,1-2H3

SMILES string

COc1ccc(OC)c2ccccc12

assay

≥99.5% (HPLC)

fluorescence

λex 318 nm; λem 394 nm in ethanol (1 mg/mL)

suitability

suitable for fluorescence

storage temp.

2-8°C

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Application

1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
064731/1V
064731/1
64731/1

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Samik Upadhaya et al.
Cell stem cell, 27(2), 336-345 (2020-06-27)
Adult mammalian hematopoietic stem cells (HSCs) reside in the bone marrow (BM) but can be mobilized into blood for use in transplantation. HSCs interact with BM niche cells that produce growth factor c-Kit ligand (Kitl/SCF) and chemokine CXCL12, and were
M Abdel-Mogib et al.
Die Pharmazie, 57(4), 286-287 (2002-05-10)
Chromatographic separation of an ethanolic extract of rhizomes of Asphodelus tenuifolius Cav. (Asphodelaceae) yielded in addition to beta-sitosterol, stigmasterol and two anthraquinone derivatives, 1,8-dimethoxynaphthalene as well as two new naphthalene derivatives. The new compounds were identified as 2-acetyl-8-methoxy-3-methyl-1-naphthol and 2-acetyl-1,8-dimethoxy-3-methylnaphthalene.
Cécile Pégurier et al.
Bioorganic & medicinal chemistry, 11(5), 789-800 (2003-01-23)
Amido derivatives 10-18 of the corresponding oxyamines were synthesised as melatoninergic ligands by the reaction of hydroxyphtalimide with the halogeno derivatives or the corresponding alcohols using Mitsunobu reaction conditions. The affinity of the compounds for chicken brain melatonin receptors and

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