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Benzoyl isothiocyanate

CAS No.
532-55-8
Chemical Name:
Benzoyl isothiocyanate
Synonyms
NSC 29259;Benzoylthiocarbimide;Benzoylisothiocyante;BENZOYL ISOTHIOCYANATE;Epinastine Impurity 29;N-BENZOYLISOTHIOCYANATE;BenzoylIsothiocyanate>Benzoyl isothiocyate, 98%;Chloropyramine Impurity 3;Benzoyl isothiocyanate 98%
CBNumber:
CB8116176
Molecular Formula:
C8H5NOS
Molecular Weight:
163.2
MDL Number:
MFCD00004815
MOL File:
532-55-8.mol
MSDS File:
SDS
Last updated:2024-08-07 10:33:10

Benzoyl isothiocyanate Properties

Melting point 128 °C
Boiling point 128-131 °C/15 mmHg (lit.)
Density 1.214 g/mL at 25 °C (lit.)
refractive index n20/D 1.6354(lit.)
Flash point >230 °F
storage temp. 2-8°C
solubility Chloroform
form Liquid
color Clear yellow to orange-brown
Specific Gravity 1.214
Water Solubility almost insoluble
Sensitive Moisture Sensitive/Lachrymatory
Merck 14,1114
BRN 606716
CAS DataBase Reference 532-55-8(CAS DataBase Reference)
FDA UNII U8J7Q32B86
NIST Chemistry Reference Benzoyl isothiocyanate(532-55-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS06
Signal word  Danger
Hazard statements  H301-H317-H318
Precautionary statements  P280-P301+P310+P330-P302+P352-P305+P351+P338+P310
Hazard Codes  T,Xi
Risk Statements  25-32-36-43-42/43-36/37/38-20/21/22
Safety Statements  26-36/37-45-36/37/39
RIDADR  UN 2810 6.1/PG 3
WGK Germany  3
Hazard Note  Lachrymatory/Moisture Sensitive
TSCA  T
HazardClass  6.1
PackingGroup  III
HS Code  29309070
NFPA 704
1
3 1

Benzoyl isothiocyanate price More Price(30)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 261653 Benzoyl isothiocyanate 98% 532-55-8 5g $52.5 2024-03-01 Buy
Sigma-Aldrich 261653 Benzoyl isothiocyanate 98% 532-55-8 25g $111 2024-03-01 Buy
TCI Chemical I0501 Benzoyl Isothiocyanate >97.0%(GC) 532-55-8 5g $38 2024-03-01 Buy
TCI Chemical I0501 Benzoyl Isothiocyanate >97.0%(GC) 532-55-8 25g $120 2024-03-01 Buy
Alfa Aesar L06964 Benzoyl isothiocyanate, 98% 532-55-8 5g $40.65 2024-03-01 Buy
Product number Packaging Price Buy
261653 5g $52.5 Buy
261653 25g $111 Buy
I0501 5g $38 Buy
I0501 25g $120 Buy
L06964 5g $40.65 Buy

Benzoyl isothiocyanate Chemical Properties,Uses,Production

Description

Benzoyl isothiocyanate is a chemical compound commonly used in organic synthesis and as a reagent in the pharmaceutical industry. It finds applications in producing dyes, pesticides, and pharmaceutical intermediates. Safety precautions must be taken when handling this compound as it can irritate the skin, eyes, and respiratory system. It should be stored in a tightly sealed container from heat sources or open flames. Proper ventilation and personal protective equipment such as gloves and goggles should be used during handling. Benzoyl isothiocyanate may have environmental impacts if not properly disposed of according to local regulations. Not for human consumption.

Chemical Properties

CLEAR YELLOW TO ORANGE-BROWN LIQUID

Uses

Benzoyl isothiocyanate has been used in the preparation of:

  • 1-benzoyl-3-(5-chloro-2-hydroxyphenyl)thiourea, new thiourea derivative
  • guanine

Properties and Applications

Benzoyl isothiocyanate (BI), as a new type of comonomer, has attracted particular attention because the structure of BI contains not only a benzene ring but also an amino group. Remarkably, the introduction of a benzene ring can be used as a D unit, and amino groups in BI were bonded with the tri-s-triazine units through thermal polymerization. BI as a precursor is used to design the UCN-based D-A conjugated copolymers by copolymerization with urea, which can favour forward intramolecular charge separation to achieve excellent photocatalytic activity and AQE in photocatalytic H2 evolution. The obtained UCN-BIx D-A conjugated copolymers possess fast forward direction charge transfer and a broad absorption range of visible light and a large specific surface area with many reactive sites. In addition, the UCN-BI400 D-A conjugated copolymer also exhibits good crystallinity and higher conduction band (CB) position than pure g-C3N4[1].

Purification Methods

Distil the isothiocyanate over a small amount of P2O5, whereby the distillate crystallises in prisms. It is readily hydrolysed by H2O to give benzamide and benzoylurea, but with NH3 it gives benzoylurea m 210o which can be recrystallised from EtOH. [Hill & Degnan J Am Chem Soc 62 1595 1940, Terss & McEwen J Am Chem Soc 76 580 1954, Frank & Smith Org Synth Coll Vol III 735 1955, Beilstein 9 IV 777.]

References

[1] Huinan Che . “Benzoyl isothiocyanate as a precursor to design of ultrathin and high-crystalline g-C3N4-based donor–acceptor conjugated copolymers for superior photocatalytic H2 production.” Chemical Engineering Journal 410 (2021): Article 127791.

333-20-0
98-88-4
532-55-8
Synthesis of Benzoyl isothiocyanate from Potassium thiocyanate and Benzoyl chloride
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View Lastest Price from Benzoyl isothiocyanate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Benzoyl isothiocyanate pictures 2019-07-06 Benzoyl isothiocyanate
532-55-8
US $1.00 / kg 1kg 96%-99% as request Career Henan Chemical Co
Benzoylthiocarbimide ISOTHIOCYANIC ACID BENZOYL ESTER BENZOYL ISOTHIOCYANATE N-BENZOYLISOTHIOCYANATE Benzoylisothiocyante Isothiocyanic acid, anhydride with benzoic acid Benzoyl isothiocyanate,98% Benzoyl isothiocyanate ,96% Benzoyl isothiocyanate, 98% 5GR NSC 29259 Benzoyl isothiocyanate 98% Benzoyl isothiocyanate benzoic acid Benzoic acid, anhydride with HNCS Benzoic acid, anhydride with isothiocyanic acid Benzoyl isothiocyate, 98% BenzoylIsothiocyanate> Epinastine Impurity 29 Chloropyramine Impurity 3 532-55-8 C6H5CONCS Organic Building Blocks Sulfur Compounds Thiocyanates/Isothiocyanates Building Blocks Aromatics Miscellaneous Reagents Phenyl isocyanate&Phenyl isothiocyanate Organic Building Blocks Sulfur Compounds Thiocyanates/Isothiocyanates