Skip to Content
Merck
All Photos(1)

Key Documents

13423

Sigma-Aldrich

Sodium chloride

puriss., meets analytical specification of Ph. Eur., BP, USP, 99.0-100.5% (calc. to the dried substance), ≤0.00002% Al

Synonym(s):

Halite, NaCl

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
NaCl
CAS Number:
Molecular Weight:
58.44
Beilstein:
3534976
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21
Assay:
99.0-100.5% (calc. to the dried substance)
form:
powder or crystals

vapor pressure

1.33 hPa ( 865 °C)

Quality Level

grade

puriss.

Assay

99.0-100.5% (calc. to the dried substance)

form

powder or crystals

quality

meets analytical specification of Ph. Eur., BP, USP

impurities

acidity or alkalinity, in accordance
hexacyanoferrate(II), in accordance
organic volatile impurities, complies (GC)
residual solvents, in accordance
≤0.00002% Al
≤0.0001% hexacyanoferrate (II)
≤0.0005% heavy metals (as Pb)
≤0.001% free acid (as HCl)
≤0.002% free alkali (as NaOH)
≤0.01% Mg and alkaline earth metals (as Ca)

loss

≤0.5% loss on drying, 105°C, 2 h

pH

7

mp

801 °C (lit.)

anion traces

bromide (Br-): ≤50 mg/kg
iodide (I-): in accordance
nitrite (NO2-): in accordance
phosphate (PO43-): ≤25 mg/kg
sulfate (SO42-): ≤200 mg/kg

cation traces

Al: ≤0.2 mg/kg
As: ≤1 mg/kg
Ba: ≤2 mg/kg
Fe: ≤2 mg/kg
K: ≤500 mg/kg

suitability

complies for appearance of solution
complies for identity

SMILES string

[Na+].[Cl-]

InChI

1S/ClH.Na/h1H;/q;+1/p-1

InChI key

FAPWRFPIFSIZLT-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

General description

(S)-(+)-Glycidyl benzyl ether is a chiral building block that can be prepared from (S)-glycidyl tosylate.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

"Determination of four heterocyclic insecticides by ionic liquid dispersive liquid?liquid microextraction in water samples"
Liu Y, et al.
Journal of Chromatography A, 1216(06), 885- 891 (2009)
A two-step synthesis of (R)-and (S)-benzylglycidyl ether
Byun HS and Bittman R
Tetrahedron Letters, 30(21), 2751-2754 (1989)
Stereoselective synthesis of 2, 6-trans-tetrahydropyran via primary diamine-catalyzed oxa-conjugate addition reaction of a, ?-unsaturated ketone: Total synthesis of Psymberin
Byeon SR, et al
Organic Letters, 13(21), 5816-5819 (2011)
A Divergent Enantioselective Synthesis of 9-J1-Phytoprostane and 9-A1-Phytoprostane Methyl Ester
Porta A, et al.
European Journal of Organic Chemistry, 2014(10), 2111-2119 (2014)
Michael T Crimmins et al.
Journal of the American Chemical Society, 126(40), 12790-12791 (2004-10-08)
The enantioselective synthesis of the potent, selective, cytotoxic, annonaceous acetogenin, (+)-gigantecin, has been completed. An asymmetric glycolate aldol serves to establish the stereocenters at C13,14 and at C21,22. A Carreira asymmetric acetylide addition is used to establish the C17 stereocenter.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service