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About This Item
Empirical Formula (Hill Notation):
AlCl3
CAS Number:
Molecular Weight:
133.34
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
InChI
1S/Al.3ClH/h;3*1H/q+3;;;/p-3
SMILES string
Cl[Al](Cl)Cl
InChI key
VSCWAEJMTAWNJL-UHFFFAOYSA-K
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
packaging
ampule of
concentration
1.00 g/L
solubility
H2O: soluble
Preparation Note
prepared with AlCl3.6H2O and H2O
signalword
Warning
hcodes
pcodes
Hazard Classifications
Met. Corr. 1
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Diagnosis and management of hyperhidrosis.
R A Benson et al.
BMJ (Clinical research ed.), 347, f6800-f6800 (2013-11-28)
Amira Zaky et al.
BMC neuroscience, 14, 26-26 (2013-03-19)
Chronic administration of Aluminum is proposed as an environmental factor that may affect several enzymes and other biomolecules related to neurotoxicity and Alzheimer's disease (AD). APE1 a multifunctional protein, functions in DNA repair and plays a key role in cell
Hai-hua Zhao et al.
Behavioural brain research, 241, 228-234 (2012-12-12)
Environmental agent aluminum, a well-known neurotoxin, has been proposed to play a role in the development of Alzheimer's disease (AD), and produced clinical and pathological features which were strikingly similar to those seen in AD brain, such as neurofibrillary tangles.
Manal Fouad Ismail et al.
International journal of nanomedicine, 8, 393-406 (2013-02-05)
To sustain the effect of rivastigmine, a hydrophilic cholinesterase inhibitor, nanobased formulations were prepared. The efficacy of the prepared rivastigmine liposomes (RLs) in comparison to rivastigmine solution (RS) was assessed in an aluminium chloride (AlCl(3))-induced Alzheimer's model. Liposomes were prepared
Bagineni Prasad et al.
Chemical communications (Cambridge, England), 48(84), 10434-10436 (2012-09-20)
A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved via AlCl(3) mediated unexpected regioselective sulfonyl group migration for N-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of Mycobacterium tuberculosis H37Rv chorismate mutase.
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