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Safety Information

187313

Sigma-Aldrich

2-Naphthalenemethanol

98%

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About This Item

Linear Formula:
C10H7CH2OH
CAS Number:
1592-38-7
Molecular Weight:
158.20
MDL number:
MFCD00004124
UNSPSC Code:
12352100
eCl@ss:
39020101
PubChem Substance ID:
24851267
NACRES:
NA.22

Quality Level

100

Assay

98%

form

powder

mp

79-81 °C (lit.)

functional group

hydroxyl

SMILES string

OCc1ccc2ccccc2c1

InChI

1S/C11H10O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7,12H,8H2

InChI key

MFGWMAAZYZSWMY-UHFFFAOYSA-N

Application

2-Naphthalenemethanol was used as marker in the determination of critical micelle concentration of anionic surfactants by capillary electrophoresis. It was used in the synthesis of acetate protected xylosides.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

187313-25G:
187313-5G:
187313-BULK:
187313-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBB0036V
11996LKV
11996LK
06701TE
00228PD

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Anton Kulikov et al.
The Journal of organic chemistry, 73(19), 7611-7615 (2008-09-11)
Irradiation of alcohols, phenols, and carboxylic acids "caged" with the (3-hydroxy-2-naphthalenyl)methyl group results in fast (k(release) approximately = 10(5) s(-1)) release of the substrates with good quantum (Phi = 0.17-0.26) and chemical (>90%) yields. The initial byproduct of the photoreaction
Karin Holmqvist et al.
Bioorganic & medicinal chemistry, 21(11), 3310-3317 (2013-04-23)
Proteoglycans (PGs) are important macromolecules in mammalian cells, consisting of a core protein substituted with carbohydrate chains, known as glycosaminoglycans (GAGs). Simple xylosides carrying hydrophobic aglycons can enter cells and act as primers for GAG chain synthesis, independent of the
T P Binder et al.
Molecular pharmacology, 33(4), 477-479 (1988-04-01)
Aryl sulfotransferase (AST) IV catalyzes the 3'-phosphoadenosine 5'-phosphosulfate-dependent sulfation of a variety of benzylic alcohols. Several molecular characteristics of benzylic alcohols were investigated for their ability to influence the catalytic efficiency of a homogeneous preparation of rat hepatic AST IV.
Determination of critical micelle concentration of anionic surfactants by capillary electrophoresis using 2-naphthalenemethanol as a marker for micelle formation.
Nakamura H, et al.
Analytical Sciences, 14(2), 379-382 (1998)
Fanyu Zhang et al.
Nature communications, 11(1), 1431-1431 (2020-03-20)
The production of 2D metal-organic frameworks (MOFs) with highly exposed active surfaces is of great importance for catalysis. Here we demonstrate the formation of MOF nanosheets by utilizing CO2 as a capping agent to control the oriented growth of MOF. This

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