Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Di(thiocyanic acid)4,4'-iminodiphenyl ester, commonly known as BPTI, is a chemical compound characterized by its white to light yellow powder form and a strong odor. It is predominantly utilized as a curing agent in the rubber industry, where it plays a crucial role in the vulcanization process.

5339-39-9

Post Buying Request

5339-39-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5339-39-9 Usage

Uses

Used in Rubber Industry:
Di(thiocyanic acid)4,4'-iminodiphenyl ester is used as a curing agent for enhancing the vulcanization process of rubber. It serves as an accelerant, promoting the cross-linking of rubber molecules, which in turn improves the mechanical properties and stability of rubber products such as tires, conveyor belts, and hoses.
Safety Considerations:
Due to its potential skin and eye irritant properties, Di(thiocyanic acid)4,4'-iminodiphenyl ester should be handled with care, adhering to established safety guidelines to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 5339-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5339-39:
(6*5)+(5*3)+(4*3)+(3*9)+(2*3)+(1*9)=99
99 % 10 = 9
So 5339-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H9N3S2/c15-9-18-13-5-1-11(2-6-13)17-12-3-7-14(8-4-12)19-10-16/h1-8,17H

5339-39-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-thiocyanatoanilino)phenyl] thiocyanate

1.2 Other means of identification

Product number -
Other names iminodibenzene-4,1-diyl bis(thiocyanate)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5339-39-9 SDS

5339-39-9Downstream Products

5339-39-9Relevant articles and documents

Thiocyanation of aromatic and heteroaromatic compounds using polymer-supported thiocyanate ion as the versatile reagent and ceric ammonium nitrate as the versatile single-electron oxidant

Karimi Zarchi, Mohammad Ali,Banihashemi, Reza

, p. 282 - 295 (2016/06/01)

ABSTRACT: Indoles, pyrrole aniline derivatives and aromatic amino compounds undergo smooth thiocyanation with cross-linked poly (4-vinylpyridine) supported thiocyanate ion, [P4-VP]SCN in the presence of ceric ammonium nitrate (CAN) as a versati

Ammonium metavanadate/thiocyanate-triggered electrophilic thiocyanation of aromatic and heteroaromatic compounds in aqueous bisulfate and acetonitrile media

Venkatesham,Rajendar Reddy,Rajanna,Veerasomaiah

, p. 606 - 612 (2015/10/19)

The ammonium metavanadate/thiocyanate system is used as an efficient reagent for regioselective thiocyanation of aromatic and hetero aromatic compounds under conventional and nonconventional conditions such as ultrasonically assisted and microwave-assisted reactions. The reactions proceeded smoothly and afforded good yields of products with high regioselectivity. Longer reaction times (about 8 h) observed under conventional conditions were reduced to 0.5 h/30 min under sonication and to 90 s in the case of microwave-assisted reactions.

Green and Efficient Method for Thiocyanation of Aromatic and Heteroaromatic Compounds Using Cross-linked Poly (4-Vinylpyridine) Supported Thiocyanate Ion as Versatile Reagent and Oxone as Mild Oxidant

Ali, Mohammad,Zarchi, Karimi,Banihashemi

, p. 1378 - 1390 (2015/10/29)

A green and efficient regioselective thiocyanation of indoles, anilines and pyrrole has been achieved via a simple protocol using cross-linked poly (4-vinylpyridine) supported thiocyanate ion, [P4-VP]SCN, as a versatile polymeric reagent and ox

An efficient and regioselective thiocyanation of aromatic and heteroaromatic compounds using cross-linked poly (4-vinylpyridine)-supported thiocyanate as a versatile reagent and potassium peroxydisulfate as a strong oxidizing agent

Karimi Zarchi,Banihashemi

, p. 458 - 469 (2014/06/10)

A green and regioselective thiocyanation of aromatic and heteroaromatic compounds has been achieved via a simple protocol using cross-linked poly (4-vinylpyridine)-supported thiocyanate ion, [P4-VP]SCN, as a versatile polymeric reagent and potassium persulfate as a strong oxidizing agent, under heterogeneous conditions.Various indoles, phenol and aniline derivatives, and pyrroles were transformed into their corresponding aryl thiocyanates in high to excellent yields. This procedure offers advantages such as short reaction time, simple reaction work-up, and the polymeric reagents can be regenerated and reused for several times without significant loss of their activity.

Electrochemical thiocyanation of nitrogen-containing aromatic and heteroaromatic compounds

Fotouhi, Lida,Nikoofar, Kobra

, p. 2903 - 2905 (2013/06/27)

An efficient and convenient anodic thiocyanation of nitrogen-containing (hetero)aromatic compounds is described under constant current conditions in the presence of ammonium thiocyanate in methanol at room temperature. We have examined the in situ thiocya

DDQ-promoted thiocyanation of aromatic and heteroaromatic compounds

Memarian, Hamid R.,Mohammadpoor-Baltork, Iraj,Nikoofar, Kobra

, p. 930 - 937 (2008/03/27)

Thiocyanation of various aromatic and heteroaromatic compounds has been achieved using ammonium thiocyanate in the presence of 2,3-dichloro-5,6- dicyanobenzoquinone (DDQ) in methanol solution at room temperature and under reflux condition. The rate of rea

A direct synthesis of aryl thiocyanates using cerium(IV) ammonium nitrate

Nair,George,Nair,Panicker

, p. 1195 - 1196 (2007/10/03)

An easy method for the conversion of arenes to aryl thiocyanates in high yields as illustrated by the formation of 3-thiocyanato indole from indole in quantitative yield is described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5339-39-9