80353
TDA Reagent
suitable for microbiology
Synonym(s):
Iron(III) chloride solution, Tryptophan Deaminase Reagent, Ferric chloride solution
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About This Item
Linear Formula:
FeCl3
CAS Number:
Molecular Weight:
162.20
NACRES:
NA.85
PubChem Substance ID:
UNSPSC Code:
41171621
MDL number:
agency
according to ISO 10273:2017
Quality Level
product line
BioChemika
form
liquid
shelf life
limited shelf life, expiry date on the label
composition
ferric chloride, 1 g/10 mL (in distilled water)
technique(s)
microbe id | specific enzyme detection: suitable
application(s)
clinical testing
food and beverages, microbiology
suitability
Proteus spp.
SMILES string
Cl[Fe](Cl)Cl
InChI
1S/3ClH.Fe/h3*1H;/q;;;+3/p-3
InChI key
RBTARNINKXHZNM-UHFFFAOYSA-K
Application
For identification of Proteus species by detection of tryptophan deaminase activity.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2
Storage Class
12 - Non Combustible Liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Insulin-like growth factor binding protein-1 (IGFBP-1) constitutes a subgroup of the insulin-like growth factor binding protein systems, and its concentration in amniotic fluid is 100-1000 times higher than the concentration in other body fluids. The aim of this study was
Abdelwareth A O Sarhan et al.
Chemical Society reviews, 38(9), 2730-2744 (2009-08-20)
In this critical review, the use of iron(III) chloride in oxidative C-C couplings of arenes and related unsaturated compounds is presented and reviewed. The approach allows highly selective dimerisations of phenol derivatives, naphthols, and heterocyclic compounds. Sequential couplings give access
Xiaoqing Li et al.
The Journal of organic chemistry, 78(18), 9499-9504 (2013-08-28)
Halosulfonylation of terminal alkynes was achieved with sulfonylhydrazides as the sulfonyl precursor and inexpensive iron halide as halide source in the presence of TBHP, allowing the regio- and stereoselective generation of (E)-β-chloro and bromo vinylsulfones.