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170518

Sigma-Aldrich

1-Naphthyl isocyanate

98%

Synonym(s):

α-Naphthyl isocyanate, 1-Isocyanatonaphthalene, 1-Naphthalene isocyanate, Naphthalen-1-ylisocyanate

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About This Item

Linear Formula:
C10H7NCO
CAS Number:
86-84-0
Molecular Weight:
169.18
Beilstein/REAXYS Number:
742779
EC Number:
201-703-7
MDL number:
MFCD00003881
UNSPSC Code:
12352100
PubChem Substance ID:
24850308
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.6344 (lit.)

bp

267 °C/761 mmHg (lit.)

mp

4 °C (lit.)

solubility

alcohol: soluble
chloroform: soluble
diethyl ether: soluble

density

1.177 g/mL at 25 °C (lit.)

SMILES string

O=C=Nc1cccc2ccccc12

InChI

1S/C11H7NO/c13-8-12-11-7-3-5-9-4-1-2-6-10(9)11/h1-7H

InChI key

BDQNKCYCTYYMAA-UHFFFAOYSA-N

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Application

1-Naphthyl isocyanate was used in the preparation of cationic aromatic urethane.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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T Ullrich et al.
Biomedical chromatography : BMC, 15(3), 212-216 (2001-06-08)
A method for determining the enantiomers of 10 therapeutically relevant aminoalcohols using HPLC and precolumn derivatization was developed. Naphthyl isocyanate reacted with racemic aminoalcohols to form urea derivatives which were separated isocratically on a cellulose tris(3,5-dimethylphenylcarbamate) coated silica gel column
Q Yang et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 24(4), 285-289 (1989-01-01)
alpha-Naphthyl isocyanate (NI) as a derivatizing agent to separate several beta-blockers was described. This procedure is simple, rapid and gives good resolution. Experiments with NI derivatives of alprenolol showed that the isocyanate group reacted with the amino group on the
Ming-Ling Chang et al.
World journal of gastroenterology, 11(27), 4167-4172 (2005-07-15)
To build up the research models of hepatic fibrosis in mice. Inbred wild-type FVB/N mice were either treated with alpha-naphthyl-isothiocyanate (ANIT), allyl alcohol (AA), carbon tetrachloride (CCl(4)), 3,5-diethoxycarbonyl-1,4-dihydrocollidine (DDC), and silica, or subjected to common bile duct ligation (CBDL) to
Desheng Zhai et al.
Planta medica, 73(2), 128-133 (2007-01-09)
Alpha-naphthyl isothiocyanate (ANIT) is a known hepatotoxicant that causes acute cholestatic hepatitis characterized by the infiltration of neutrophils around bile ducts and necrotic hepatocytes. The effects of glycyrrhizin (GL), 18beta-glycyrrhetinic acid (GA), matrine (MT), oxymatrine (OMT), salvianolic acid B (SAB)
Shashi K Ramaiah et al.
Toxicologic pathology, 35(6), 757-766 (2007-10-19)
Polymorphonuclear leukocytes (neutrophils) are essential in the defense against invading microorganisms, tissue trauma or any inciting inflammatory signals. Hepatic infiltration of neutrophils is an acute response to recent or ongoing liver injury, hepatic stress or unknown systemic inflammatory signals. Once
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