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2-Naphthalenethiol

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2-Naphthalenethiol Basic information

Product Name:
2-Naphthalenethiol
Synonyms:
  • 2-Metcaptonaphthalene
  • 2-Naphthyl thiol
  • 2-naphthylthiol
  • beta-Mercaptonaphthalene
  • beta-Naphthyl mercaptan
  • beta-naphthylmercaptan
  • mercaptanbeta-naphtalenique
  • naphthalenethiol(non-specificname)
CAS:
91-60-1
MF:
C10H8S
MW:
160.24
EINECS:
202-082-5
Product Categories:
  • Industrial/Fine Chemicals
  • Phenol&Thiophenol&Mercaptan
Mol File:
91-60-1.mol
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2-Naphthalenethiol Chemical Properties

Melting point:
79-81 °C (lit.)
Boiling point:
286 °C (lit.)
Density 
1.22
refractive index 
1.589-1.591
FEMA 
3314 | 2-NAPHTHALENTHIOL
Flash point:
69 °C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
diethyl ether: very soluble(lit.)
form 
Powder
pka
6?+-.0.30(Predicted)
color 
Almost white to cream
Odor
at 0.10 % in propylene glycol. sulfurous rubbery meaty roasted woody creamy artichoke
Odor Type
sulfurous
Water Solubility 
Soluble in alcohol, dipropylene glycol. Soluble in water 34.4 mg/L @ 25°C.
Sensitive 
Air Sensitive
Merck 
14,6379
JECFA Number
531
BRN 
636389
LogP
3.75
CAS DataBase Reference
91-60-1(CAS DataBase Reference)
NIST Chemistry Reference
2-Naphthalenethiol(91-60-1)
EPA Substance Registry System
2-Naphthalenethiol (91-60-1)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-20/21/22
Safety Statements 
36/37
RIDADR 
UN 3335
WGK Germany 
3
RTECS 
QK3930000
13
Hazard Note 
Harmful/Irritant
TSCA 
Yes
HS Code 
29309070

MSDS

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2-Naphthalenethiol Usage And Synthesis

Description

2-Naphthalenthiol has a disagreeable mercaptan-like odor. May be prepared by catalytic hydrogenation of a sulfonic acid derivative of naphthalene; by reduction of naphthalenesulfonyl chloride with zinc.

Chemical Properties

2-Naphthyl mercaptan has a disagreeable sulfurous, mushroom, meaty odor

Chemical Properties

Almost white to cream powder

Uses

2-Thionaphthol was used in the preparation of cholesterol monolayer and multilayer Langmuir- Blodgett (LB) films. The magnetic resonance shift for a self-assembled monolayer of 2-naphthalenethiol was studied that suggested considerable promise in flexible and transparent photonic devices for biological and chemical sensing.

Preparation

By catalytic hydrogenation of a sulfonic acid derivative of naphthalene; by reduction of naphthalenesulfonyl chloride with zinc.

Definition

ChEBI: 2-Naphthalenethiol is a member of naphthalenes.

Taste threshold values

Taste characteristics at 10 ppm: sulfurous, meaty, brown, roasted, chicken, eggy with a slight nutty nuance

Synthesis Reference(s)

The Journal of Organic Chemistry, 31, p. 3980, 1966 DOI: 10.1021/jo01350a023
Tetrahedron Letters, 37, p. 4523, 1996 DOI: 10.1016/0040-4039(96)00873-8

General Description

The magnetic resonance shift for a self-assembled monolayer of 2-naphthalenethiol was studied that suggested considerable promise in flexible and transparent photonic devices for biological and chemical sensing.

Safety Profile

Poison by ingestion and intraperitoneal routes. A mosquito larvicide. When heated to decomposition it emits highly toxic fumes of SOx.

Purification Methods

It is steam volatile. It has to be distilled under Ar or N2, as it oxidises to the disulfide, and crystallises from EtOH. The S-methyl derivative has m 104-105o (from *C6H6/pet ether), and the S-ethyl derivative M 188.2, has m 16o and b 175-170.5o/15mm. The S-acetate has m 53.5o and b 191o/15mm, and the diethylamine salt forms yellow needles m 107o from dioxane. [Beilstein 6 H 657, 6 I 316, 6 II 610, 6 III 3006, 6 IV 4312.]

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