TDA Reagent

Name: TDA Reagent
Brand: SIAL

suitable for microbiology

Synonym(s):

Iron(III) chloride solution, Tryptophan Deaminase Reagent, Ferric chloride solution

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All Photos(1)

About This Item

Linear Formula:

FeCl₃

CAS Number:

7705-08-0

Molecular Weight:

162.20

NACRES:

NA.85

PubChem Substance ID:

329768816

UNSPSC Code:

41171621

MDL number:

MFCD00011005

Product Name

TDA Reagent, suitable for microbiology

InChI key

RBTARNINKXHZNM-UHFFFAOYSA-K

SMILES string

Cl[Fe](Cl)Cl

InChI

1S/3ClH.Fe/h3*1H;/q;;;+3/p-3

agency

according to ISO 10273:2017

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.

Quality Level

200

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Related Categories

Bioprocessing Cell Culture

Bioprocessing Recombinant Supplements

Industrial Microbiology

Microbial Identification Tests

Pharma & Biopharma Manufacturing

Application

For identification of Proteus species by detection of tryptophan deaminase activity.

pictograms

GHS05,GHS09

signalword

Danger

hcodes

H290,H315,H318,H411

pcodes

P234 - P264 - P273 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Clinical application of immunomagnetic reduction for quantitative measurement of insulin-like growth factor binding protein-1 in the prediction of pregnant women with preterm premature rupture of membranes.

Chen-Yu Chen et al.

Clinica chimica acta; international journal of clinical chemistry, 438, 337-341 (2014-10-05)

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

Iron(III) chloride in oxidative C-C coupling reactions.

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

Formation of iron containing aggregates at the liquid-air interface.

D C Florian Wieland et al.

Colloids and surfaces. B, Biointerfaces, 109, 74-81 (2013-04-27)

The early stages of the formation of inorganic aggregates, composed of iron compounds at the solution-air interface, were investigated in situ. The properties of the solution-air interface were changed by using different Langmuir layers. In order to get insight into

FeCl3 catalyzed Prins-type cyclization for the synthesis of highly substituted indenes: application to the total synthesis of (±)-jungianol and epi-jungianol.

Dattatraya H Dethe et al.

Organic letters, 15(3), 429-431 (2013-01-16)

A novel approach was developed for the synthesis of highly substituted indene derivatives, using an FeCl(3) catalyzed Prins-type cyclization reaction which was further applied in the total synthesis of jungianol and epi-jungianol.

Iron halide-mediated regio- and stereoselective halosulfonylation of terminal alkynes with sulfonylhydrazides: synthesis of (E)-β-chloro and bromo vinylsulfones.

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.

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