Skip to Content
Merck
CN

131482

4-Phenylthiosemicarbazide

99%

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C6H5NHCSNHNH2
CAS Number:
5351-69-9
Molecular Weight:
167.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848018
EC Number:
226-329-1
Beilstein/REAXYS Number:
608285
MDL number:
MFCD00007615
Assay:
99%
Form:
solid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

4-Phenylthiosemicarbazide, 99%

InChI key

KKIGUVBJOHCXSP-UHFFFAOYSA-N

InChI

1S/C7H9N3S/c8-10-7(11)9-6-4-2-1-3-5-6/h1-5H,8H2,(H2,9,10,11)

SMILES string

NNC(=S)Nc1ccccc1

assay

99%

form

solid

mp

138-140 °C (lit.)

functional group

amine
hydrazine
thiourea

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

4-Phenylthiosemicarbazide was used in the synthesis of amberlite XAD resins. It was also used in the synthesis of a series of thiosemicarbazones.

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H300

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN7637
BCCJ9608
BCCF7529
BCCC7734
BCBX0982

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Justin W Hicks et al.
Chemistry & biodiversity, 5(11), 2415-2422 (2008-11-28)
Addition of thiosemicarbazide, 4-allylthiosemicarbazide, and 4-phenylthiosemicarbazide to (formylphenyl)boronic acids affords a series of thiosemicarbazones containing boronic acids. Addition of 2-formylphenylboronic acid to the thiosemicarbazides gave the corresponding cyclic 2,3,1-benzodiazaborines. All new compounds have been investigated for potential antifungal activity.
Derya Kara et al.
Journal of hazardous materials, 165(1-3), 1165-1169 (2008-12-17)
A matrix separation and analyte preconcentration system using Amberlite XAD copolymer resins functionalized by Schiff base reactions coupled with atomic spectrometry has been developed. Three different functionalized Amberlite XAD resins were synthesized using 4-phenylthiosemicarbazide, 2,3-dihydroxybenzaldehyde and 2-thiophenecarboxaldehyde as reagents. These

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service