Lithium perchlorate trihydrate

Names

[ CAS No. ]:
13453-78-6

[ Name ]:
Lithium perchlorate trihydrate

[Synonym ]:
lithium,perchlorate,trihydrate
EINECS 232-237-2
MFCD00149765

Chemical & Physical Properties

[ Density]:
1.841 g/mL at 25 °C(lit.)

[ Melting Point ]:
95 °C

[ Molecular Formula ]:
ClH₆LiO₇

[ Molecular Weight ]:
160.43700

[ Exact Mass ]:
159.99600

[ PSA ]:
101.96000

[ LogP ]:
0.02140

[ Water Solubility ]:
597 g/L (25 ºC)

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: SC8750000

CHEMICAL NAME :: Perchloric acid, lithium salt, trihydrate

CAS REGISTRY NUMBER :: 13453-78-6

LAST UPDATED :: 199307

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: Cl-O4.Li.3H2-O

MOLECULAR WEIGHT :: 160.45

WISWESSER LINE NOTATION :: LI G-O4 &QH 3

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 1160 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: JAFCAU Journal of Agricultural and Food Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB 57136, West End Stn., Washington, DC 20037) V.1- 1953- Volume(issue)/page/year: 14,512,1966

Safety Information

[ Symbol ]:

GHS03, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H272-H315-H319-H335

[ Precautionary Statements ]:
P220-P261-P305 + P351 + P338

[ Hazard Codes ]:
O:Oxidizingagent;Xi:Irritant;

[ Risk Phrases ]:
R36/37/38;R8

[ Safety Phrases ]:
S17-S26-S27-S36/37/39-S37/39

[ RIDADR ]:
UN 1481 5.1/PG 2

[ WGK Germany ]:
1

[ RTECS ]:
SC8750000

[ Packaging Group ]:
II

[ Hazard Class ]:
5.1

Articles

Notable effects of the metal salts on the formation and decay reactions of α-tocopheroxyl radical in acetonitrile solution. The complex formation between α-tocopheroxyl and metal cations.

J. Phys. Chem. B 115(32) , 9880-8, (2011)

The measurement of the UV-vis absorption spectrum of α-tocopheroxyl (α-Toc(•)) radical was performed by reacting aroxyl (ArO(•)) radical with α-tocopherol (α-TocH) in acetonitrile solution including f...

Transformation of D-(-)-ribose into a natural product-like scaffold via a Lewis acid catalyzed intramolecular hetero-Diels-Alder reaction.

Nucleosides Nucleotides Nucleic Acids 26(6-7) , 701-4, (2007)

Starting from D-(-)-ribose, a tricyclic natural product-like scaffold suitable for combinatorial derivatization was synthesized via an intramolecular hetero-Diels-Alder reaction. Lithium perchlorate w...

Anion-induced reconstitution of a self-assembling system to express a chloride-binding Co10L15 pentagonal prism.

Nature Chemistry 4(9) , 751-6, (2012)

Biochemical systems are adaptable, capable of reconstitution at all levels to achieve the functions associated with life. Synthetic chemical systems are more limited in their ability to reorganize to ...