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78820

Supelco

1-Phenyl-1H-tetrazole-5-thiol

for spectrophotometric det. of Pd, for the determination of Bi, ≥97.0%

Synonym(s):

1-Phenyl-5-mercaptotetrazole, 1-Phenyltetrazoline-5-thione, 5-Mercapto-1-phenyltetrazole

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About This Item

Empirical Formula (Hill Notation):
C7H6N4S
CAS Number:
86-93-1
Molecular Weight:
178.21
Beilstein/REAXYS Number:
139068
EC Number:
201-710-5
MDL number:
MFCD00003129
UNSPSC Code:
12000000
PubChem Substance ID:
329768183

assay

≥97.0% (HPLC)
≥97.0%

form

powder

quality

for spectrophotometric det. of Pd
for the determination of Bi

technique(s)

UV/Vis spectroscopy: suitable

mp

145 °C (dec.) (lit.)

SMILES string

Sc1nnnn1-c2ccccc2

InChI

1S/C7H6N4S/c12-7-8-9-10-11(7)6-4-2-1-3-5-6/h1-5H,(H,8,10,12)

InChI key

GGZHVNZHFYCSEV-UHFFFAOYSA-N

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Aquatic Chronic 4 - Eye Irrit. 2 - Flam. Sol. 1 - Skin Sens. 1

Storage Class

4.1A - Other explosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBG1865V
BCBD9898V
BCBD6619V
1411286
444478/1

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Fresenius Journal of Analytical Chemistry, 261, 151-151 (1972)
Mohammad M Khodaei et al.
The Journal of organic chemistry, 73(7), 2527-2532 (2008-03-05)
In the presence of 1-phenyl-5-mercaptotetrazole as a nucleophile, electrochemical oxidations of 1,2- and 1,4-dihydroxybenzenes have been investigated in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The voltammetric results indicate that an electrooxidative/Michael-type sequential reaction occurs between the mercaptide anion
K Nesmĕrák et al.
Folia microbiologica, 45(2), 138-142 (2001-03-29)
The antifungal effect of substituted 1-phenyl-5-mercaptotetrazoles was tested with Candida tropicalis, C. pseudotropicalis, C. mogii, Trichosporon cutaneum, Cryptococcus albidus and S. cerevisiae. Candida strains exhibited the lowest sensitivity to the compounds; the most sensitive was S. cerevisiae. The MIC values
J Kejha et al.
Ceskoslovenska farmacie, 39(7), 294-298 (1990-09-01)
For the investigation of new anti-inflammatory drugs, 1-phenyl-5-mercaptotetrazole (I) was selected as the principal structure. The purpose itself lay in an alkylation of the mercapto group with different remainders. In some cases at the same time a substituent was introduced
[Information from the Soviet Toxicology Center].
Gigiena truda i professional'nye zabolevaniia, (10)(10), 55-56 (1980-10-01)

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