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14211

Supelco

Water

ACS reagent, CHROMASOLV®, suitable for HPLC and ultratrace analysis

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About This Item

Linear Formula:
H2O
CAS Number:
7732-18-5
Molecular Weight:
18.02
Beilstein:
2050024
EC Number:
231-791-2
MDL number:
MFCD00011332
UNSPSC Code:
12191602
PubChem Substance ID:
329750421
NACRES:
NA.24

product name

Water, ACS reagent, for ultratrace analysis

grade

ACS reagent
for inorganic trace analysis
for ultratrace analysis

Quality Level

100

form

liquid

technique(s)

immunofluorescence: suitable

impurities

≤5 μg/kg ammonium (NH4)

refractive index

n20/D 1.34 (lit.)

pH

6.0-8.0(-25 °C77 °F)

bp

100 °C (lit.)

mp

0 °C (lit.)

solubility

water: miscible (completely)

density

1.000 g/mL at 3.98 °C (lit.)

anion traces

bromide (Br-): ≤1 μg/kg
chloride (Cl-): ≤1 μg/kg
fluoride (F-): ≤1 μg/kg
iodide (I-): ≤1 μg/kg
nitrate (NO3-): ≤1 μg/kg
nitrite (NO2-): ≤1 μg/kg
phosphate (PO43-): ≤1 μg/kg
sulfate (SO42-): ≤1 μg/kg

cation traces

Ag: ≤0.001 μg/kg
Al: ≤0.5 μg/kg
As: ≤0.01 μg/kg
Au: ≤0.005 μg/kg
B: ≤0.5 μg/kg
Ba: ≤0.5 μg/kg
Be: ≤0.005 μg/kg
Bi: ≤0.001 μg/kg
Ca: ≤0.5 μg/kg
Cd: ≤0.5 μg/kg
Ce: ≤0.001 μg/kg
Co: ≤0.5 μg/kg
Cr: ≤0.5 μg/kg
Cs: ≤0.001 μg/kg
Cu: ≤0.5 μg/kg
Dy: ≤0.001 μg/kg
Er: ≤0.001 μg/kg
Eu: ≤0.001 μg/kg
Fe: ≤0.5 μg/kg
Ga: ≤0.001 μg/kg
Gd: ≤0.001 μg/kg
Ge: ≤0.005 μg/kg
Hf: ≤0.001 μg/kg
Hg: ≤0.5 μg/kg
Ho: ≤0.001 μg/kg
In: ≤0.001 μg/kg
Ir: ≤0.001 μg/kg
K: ≤0.5 μg/kg
La: ≤0.001 μg/kg
Li: ≤0.5 μg/kg
Lu: ≤0.001 μg/kg
Mg: ≤0.5 μg/kg
Mn: ≤0.5 μg/kg
Mo: ≤0.5 μg/kg
Na: ≤0.5 μg/kg
Nb: ≤0.005 μg/kg
Nd: ≤0.001 μg/kg
Ni: ≤0.005 μg/kg
Os: ≤0.005 μg/kg
Pb: ≤05 μg/kg
Pd: ≤0.001 μg/kg
Pr: ≤0.001 μg/kg
Pt: ≤0.005 μg/kg
Rb: ≤0.001 μg/kg
Re: ≤0.005 μg/kg
Rh: ≤0.001 μg/kg
Ru: ≤0.005 μg/kg
Sb: ≤0.001 μg/kg
Sc: ≤0.005 μg/kg
Se: ≤5 μg/kg
Si: ≤0.5 μg/kg
Sm: ≤0.001 μg/kg
Sn: ≤0.5 μg/kg
Sr: ≤0.5 μg/kg
Ta: ≤0.001 μg/kg
Tb: ≤0.001 μg/kg
Te: ≤0.001 μg/kg
Th: ≤0.005 μg/kg
Ti: ≤0.5 μg/kg
Tl: ≤0.005 μg/kg
Tm: ≤0.001 μg/kg
U: ≤0.001 μg/kg
V: ≤0.5 μg/kg
W: ≤0.005 μg/kg
Y: ≤0.001 μg/kg
Yb: ≤0.001 μg/kg
Zn: ≤0.5 μg/kg
Zr: ≤0.5 μg/kg

SMILES string

O

application(s)

sample preparation

InChI

1S/H2O/h1H2

InChI key

XLYOFNOQVPJJNP-UHFFFAOYSA-N

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Storage Class Code

12 - Non Combustible Liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL8739
BCCL4177
BCCK0014
BCCK3887
BCCH3634

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Mary A Rodgers et al.
The Journal of experimental medicine, 211(7), 1333-1347 (2014-06-25)
Linear ubiquitination is a newly discovered posttranslational modification that is currently restricted to a small number of known protein substrates. The linear ubiquitination assembly complex (LUBAC), consisting of HOIL-1L, HOIP, and Sharpin, has been reported to activate NF-κB-mediated transcription in
Rachele M Pojednic et al.
Calcified tissue international, 96(3), 256-263 (2014-12-07)
Vitamin D receptor (VDR) expression and action in non-human skeletal muscle have recently been reported in several studies, yet data on the activity and expression of VDR in human muscle cells are scarce. We conducted a series of studies to
Susu Duan et al.
Nature communications, 5, 5029-5029 (2014-10-10)
Oseltamivir-resistant H1N1 influenza viruses carrying the H275Y neuraminidase mutation predominated worldwide during the 2007-2009 seasons. Although several neuraminidase substitutions were found to be necessary to counteract the adverse effects of H275Y, the order and impact of evolutionary events involved remain
Yasushi Itoh et al.
PLoS pathogens, 10(6), e1004192-e1004192 (2014-06-20)
Highly pathogenic avian influenza (HPAI) viruses of the H5N1 subtype often cause severe pneumonia and multiple organ failure in humans, with reported case fatality rates of more than 60%. To develop a clinical antibody therapy, we generated a human-mouse chimeric
Hervé Marie-Nelly et al.
Nature communications, 5, 5695-5695 (2014-12-18)
Closing gaps in draft genome assemblies can be costly and time-consuming, and published genomes are therefore often left 'unfinished.' Here we show that genome-wide chromosome conformation capture (3C) data can be used to overcome these limitations, and present a computational
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