Sodium chloride 99-100.5% (dried basis), granular USP, FCC endotoxin tested, J.T.Baker®

Supplier: Avantor
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3629-09EA 861.68 EUR
3629-09 3629-07
Sodium chloride 99-100.5% (dried basis), granular USP, FCC endotoxin tested, J.T.Baker®
Sodium chloride

Avantor excipients are used during the formulation process in a wide range of applications. Avantor provides high-purity and performance excipients that serve as fillers, binders, disintegrants, lubicants, flavors, emulsifiers and preservatives. All the products are cGMP produced and meet USP grade standards.


  • Food GMP manufactured product

Formula: NaCl
MW: 58,44 g/mol
Boiling Pt: 1413 °C (1013 hPa)
Melting Pt: 801 °C
Density: 2,16 g/cm³
MDL Number: MFCD00003477
CAS Number: 7647-14-5
Merck Index: 14,08599

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Specification Test Results

Food GMP Manufactured Product
Meets F.C.C. Requirements
GMP Manufactured Product
Meets U.S.P Requirements
CAUTION: For Manufacturing, processing or repackaging
Bulk Pharmaceutical Chemical
Bulk Food Chemical
USP - Assay (NaCl) (USP) (dried basis) 99.0 - 100.5 %
USP - Identification A Passes Test
USP - Identification B Passes Test
USP - Acidity or Alkalinity Passes Test
USP - Aluminum (Al) ≤0.2 ppm
USP - Arsenic (As) ≤1 ppm
USP - Appearance of Solution Passes Test
USP - Barium (Ba) Passes Test
USP - Endotoxin Concentration (2.5 EU/g max.) Passes Test
USP - Nitrite (NO₂) (Absorbance Value) ≤0.01
USP - Iron (Fe) ≤2 ppm
USP - Magnesium and Alkaline Earth Metals (as Ca) ≤100 ppm
USP - Loss on Drying ≤0.5 %
USP - Iodide (I) Passes Test
USP - Bromide (Br) ≤100 ppm
USP - Ferrocyanide Passes Test
USP - Phosphate (PO₄) ≤25 ppm
USP - Potassium (K) ≤500 ppm
USP - Sulfate (SO₄) ≤200 ppm
FCC - Assay (as NaCl) (FCC) (ignited basis) 99.0 - 100.5 %
FCC - Identification A Passes Test
FCC - Identification B Passes Test
FCC - Arsenic (As) ≤1 ppm
FCC - Calcium and Magnesium (as Ca) (by EDTA titration)(FCC) ≤0.35 %
FCC - Heavy Metals (as Pb) ≤2 ppm
FCC - Iron (Fe) ≤2 ppm
FCC - Loss on Drying ≤0.5 %
No Class 1,2,3 or other solvents are used or produced in the
manufacturing or purification of the product.
Must be subjected to further processing during the preparation of
injectable dosage forms
Elemental Impurities (USP 232, EP 5.20) - Information on elemental
impurities for this product is available on the associated Product
Regulatory Data Sheet and elemental impurity profile report.

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