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1-Naphthyl isothiocyanate

Product Name
1-Naphthyl isothiocyanate
CAS No.
551-06-4
Chemical Name
1-Naphthyl isothiocyanate
Synonyms
ANI;ANIT;Kesscocide;1-Naphthyl senfoel;Naphthyl mustard oil;1-Naftylisothiokyanat;Naphthyl isothiocyanat;1-NAPTHYL ISOTHIOCYANATE;1-Naphtyl isothiocyanate;1-NAPHTHYL ISOTHIOCYANATE
CBNumber
CB8696418
Molecular Formula
C11H7NS
Formula Weight
185.24
MOL File
551-06-4.mol
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1-Naphthyl isothiocyanate Property

Melting point:
55.5-57 °C(lit.)
Boiling point:
190 °C(Press: 20 Torr)
Density 
1.1142 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
2-8°C
form 
Fine Crystalline Powder
color 
Yellow
Water Solubility 
insoluble
Sensitive 
Moisture Sensitive
Merck 
14,6411
BRN 
637868
Stability:
Stable, but moisture sensitive. Incompatible with strong oxidizing agents.
CAS DataBase Reference
551-06-4(CAS DataBase Reference)
NIST Chemistry Reference
Naphthalene, 1-isothiocyanato-(551-06-4)
EPA Substance Registry System
1-Naphthylisothiocyanate (551-06-4)
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Safety

Hazard Codes 
T
Risk Statements 
20/21-25-36/37/38-42-23/24/25
Safety Statements 
22-26-36/37-45-24/25
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
NX9100000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29309090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H315Causes skin irritation

H319Causes serious eye irritation

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
N4525
Product name
1-Naphthyl isothiocyanate
Purity
95%
Packaging
10g
Price
$173
Updated
2024/03/01
Sigma-Aldrich
Product number
18951
Product name
1-Naphthyl isothiocyanate
Purity
for HPLC derivatization, ≥98.5% (HPLC and GC)
Packaging
1g
Price
$51.2
Updated
2022/05/15
TCI Chemical
Product number
I0190
Product name
1-Naphthyl Isothiocyanate
Purity
>98.0%(GC)
Packaging
5g
Price
$85
Updated
2024/03/01
TCI Chemical
Product number
I0190
Product name
1-Naphthyl Isothiocyanate
Purity
>98.0%(GC)
Packaging
25g
Price
$265
Updated
2024/03/01
Alfa Aesar
Product number
L12418
Product name
1-Naphthyl isothiocyanate, 98%
Packaging
10g
Price
$109.65
Updated
2024/03/01
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1-Naphthyl isothiocyanate Chemical Properties,Usage,Production

Description

1-Napthylisothiocyanate is a toxic chemical that has been used to create experimental cholestasis in rodents. Laboratory studies have also shown that 1-napthylisothiocyanate can act as a chemoprotectant in rodents challenged with a tumorinducing agent such as phorbol-12 myristate 13-acetate.

Chemical Properties

white crystalline powder

Uses

1-Naphthylisothiocyanate is used as an ingredient in insecticides. It is also found in cyanamide, which is used in many industrial applications. It is commonly used in medical and drug studies in animals as a model hepatotoxicant producing experimental cholestasis in rats and mice.

Uses

1-Naphthyl isothiocyanate is a tool for the study of liver damage which causes bile stasis and hyperbilirubinemia acutely and bile duct hyperplasia and biliary cirrhosis chronically, with changes in hepatocyte function.

Uses

1-Naphthyl isothiocyanate (NITC) can be used as a source of thiourea moiety to synthesize derivatives of calix[4]arenes to be used as anion acceptors. It can also be used for the synthesis of naphthyl substituted 1,2,4-triazoles and 1,3,4-thiadiazoles.

Definition

ChEBI: 1-naphthyl isothiocyanate is an isothiocyanate. It has a role as an insecticide. It derives from a hydride of a naphthalene.

General Description

Odorless white needles or powder. Tasteless.

Air & Water Reactions

1-Naphthyl isothiocyanate is moisture sensitive. . Undergoes slow hydrolysis. Insoluble in water.

Reactivity Profile

Isocyanates and thioisocyanates, such as 1-Naphthyl isothiocyanate, are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].

Fire Hazard

Flash point data for 1-Naphthyl isothiocyanate is not available, but 1-Naphthyl isothiocyanate is probably combustible.

Environmental Fate

Naphthylisothiocyanate is moisture sensitive and insoluble in water. The hydrolysis rate is slow.

Purification Methods

Crystallise the isothiocyanate from hexane (1g in 9 mL). It forms white needles and is soluble in most organic solvents but is insoluble in H2O. It is absorbed through the skin and may cause dermatitis. [Cymmerman-Craig et al. Org Synth Coll Vol IV 700 1963, Beilstein 12 H 1244, 12 III 2948.]

Toxicity evaluation

1-Naphthylisothiocyanate causes separation of extracellular tight junctions that seal bile canaliculi, impairing bile formation. 1-Naphthylisothiocyanate inhibits microsomal drug-metabolizing activity. In rats, 1-naphthylisothiocyanteglutathione complex is formed in hepatocytes, then transported to the bile ducts, where it is released from the glutathione, and then selectively injures biliary epithelial cells, resulting in reduced bile flow.

1-Naphthyl isothiocyanate Preparation Products And Raw materials

Raw materials

Preparation Products

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1-Naphthyl isothiocyanate Suppliers

Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
Advantage
56
Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
Tel
+86-21-54098501
Fax
+86-21-54096319
Email
sales@sinch.com.cn
Country
China
ProdList
11598
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Beijing Taiya Jie Technology Development Co., Ltd.
Tel
021-33690831-8001 13552411790
Fax
021-33690831
Email
postmaster@tyjchem.cn
Country
China
ProdList
1541
Advantage
55
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View Lastest Price from 1-Naphthyl isothiocyanate manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
1-Naphthyl isothiocyanate 551-06-4
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-06-27
Career Henan Chemical Co
Product
1-Naphthyl isothiocyanate 551-06-4
Price
US $1.00/KG
Min. Order
1g
Purity
85.0-99.8%
Supply Ability
20ton
Release date
2019-12-20

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