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62528

Sigma-Aldrich

Lithium hydroxide monohydrate

BioUltra, ≥99.0% (T)

Synonym(s):

LiOH · H2O, Lithium hydroxide, Lithium hydroxide hydrate

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50 G
€39.70
250 G
€119.00
1 KG
€357.00

About This Item

Linear Formula:
LiOH · H2O
CAS Number:
1310-66-3
Molecular Weight:
41.96
EC Number:
215-183-4
MDL number:
MFCD00149772
UNSPSC Code:
12352302
PubChem Substance ID:
57651895
NACRES:
NA.25
grade:
reagent grade
form:
solid
solubility:
H2O: 1 M at 20 °C, clear, colorless

€39.70

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grade

reagent grade

product line

BioUltra

Assay

≥99.0% (T)

form

solid

impurities

insoluble matter, passes filter test

pH

~12 (25 °C, 1 M in H2O)

solubility

H2O: 1 M at 20 °C, clear, colorless

anion traces

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤100 mg/kg

cation traces

Al: ≤20 mg/kg
As: ≤0.2 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤50 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤200 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

1 M in H2O

UV absorption

λ: 260 nm Amax: 0.02
λ: 280 nm Amax: 0.02

SMILES string

[Li+].O.[OH-]

InChI

1S/Li.2H2O/h;2*1H2/q+1;;/p-1

InChI key

GLXDVVHUTZTUQK-UHFFFAOYSA-M

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Application

Lithium hydroxide, an alkaline activator/catalyst of synthetic processes, may be used in the formation of polycrystalline Li2O nanowires.

Other Notes

Titrant in the procedure for the cleavage of Asn-Gly bonds with hydroxylamine[1]

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL2817
BCCL7760
BCCK6771
BCCK0632
BCCK5049

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Cleavage at Asn-Gly bonds with hydroxylamine.
P Bornstein et al.
Methods in enzymology, 47, 132-145 (1977-01-01)
Muhammad Ayoub et al.
Bioresource technology, 112, 308-312 (2012-03-23)
The synthesis of oxygenated fuel additives via solvent freebase-catalyzed etherification of glycerol is reported. The products of glycerol etherification arediglycerol (DG) and triglycerol (TG) with DG being the favorable one. The catalytic activity of different homogeneous alkali catalysts (LiOH, NaOH
Quanling Yang et al.
Biomacromolecules, 12(7), 2766-2771 (2011-06-11)
Transparent and bendable regenerated cellulose films prepared from aqueous alkali (NaOH or LiOH)/urea (AU) solutions exhibit high oxygen barrier properties, which are superior to those of conventional cellophane, poly(vinylidene chloride), and poly(vinyl alcohol). Series of AU cellulose films are prepared
Petr Tůma et al.
Electrophoresis, 31(12), 2037-2043 (2010-06-22)
A CE procedure employing capacitively coupled contactless conductivity detection has been developed for direct determination of the glycerol and mannitol polyalcohols in biological and pharmacological samples. Both glycerol and mannitol are fully separated from the sample matrix within very short
Jie Cai et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 8(10), 1572-1579 (2007-06-15)
It was puzzling that cellulose could be dissolved rapidly in 4.6 wt % LiOH/15 wt % urea aqueous solution precooled to -12 degrees C, whereas it could not be dissolved in the same solvent without prior cooling. To clarify this
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