03797
Vanadium atomic spectroscopy standard concentrate 1.00 g V
1.00 g/L, for 1L standard solution, analytical standard
Synonym(s):
Ammonium (meta)vanadate solution
InChI
1S/V
SMILES string
[V]
InChI key
LEONUFNNVUYDNQ-UHFFFAOYSA-N
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
packaging
ampule of
solubility
H2O: soluble
Preparation Note
prepared with NH4VO3, NaOH and H2O
signalword
Danger
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 Inhalation
target_organs
Respiratory Tract
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Kazuo Kobayashi et al.
Toxicology, 228(2-3), 162-170 (2006-09-22)
Metallothionein (MT) is a low-molecular-weight cysteine-rich protein which has a high affinity for metals. The synthesis of MT is induced by heavy metals such as cadmium and zinc. However, little is known about the induction of MT by tetravalent or
H K Parsadanian et al.
Neurotoxicology, 19(4-5), 561-564 (1998-09-24)
Vanadium and its derivatives are the well-known environmental pollutants. We obtained that ammonium vanadate suppressed the alkaline (AlP) and acid (AcP) phosphatases activity in the variety of tissues. Vanadate inhibited the enzymes that take part in phosphoryl transfer reactions. Successive
Wiesława Misiuk
Pakistan journal of pharmaceutical sciences, 19(2), 87-94 (2006-06-06)
Simple and sensitive UV-VIS spectrophotometric methods for the determination of chlorprothixene hydrochloride have been developed. One of them is based on the oxidation of chlorprothixene (CPT) by ammonium metavanadate with the formation of colourless product. The second method involves the
[Vanadium poisoning].
S Khiar et al.
Annales francaises d'anesthesie et de reanimation, 29(10), 739-740 (2010-08-24)
Z Zhou et al.
The Journal of biological chemistry, 274(26), 18503-18514 (1999-06-22)
Two-thirds of the lipid A in wild-type Escherichia coli K12 is a hexa-acylated disaccharide of glucosamine in which monophosphate groups are attached at positions 1 and 4'. The remaining lipid A contains a monophosphate substituent at position 4' and a
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