Mubychem Group, established in 1976, is the pioneer manufacturer of Ammonium Chloride, Zinc Chloride etc. It has (FDA) GMP approval, ISO-9001-2008 Certificate, "REACH" Pre-registration, ISO-22000:2005 HACCP, Kosher Certificate and Halal Certificate.
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Sodium Acetate Trihydrate Anhydrous AR Pharma
GRADES AND SPECIFICATIONS OF SODIUM ACETATE TRI-HYDRATE CRYSTALS
|
SPECIFICATIONS |
SODIUM ACETATE TRIHYDRATE PURE |
SODIUM ACETATE TRIHYDRATE TECHNICAL |
|
Assay |
99% Sodium Acetate Trihydrate minimum |
98% Sodium Acetate Trihydrate minimum |
|
Appearance |
White Transparent Crystalline |
Off-White Crystalline |
|
Test Solution |
A 10% Solution is clear & colourless |
A 10% Solution is clear & colourless |
|
pH |
7.5-9 |
7.5-9 |
|
Arsenic |
Less than 1 ppm |
Less than 1 ppm |
|
Calcium & Magnesium |
Less than 50 ppm |
Less than 100 ppm |
|
Heavy Metals |
Less than 1 ppm |
Less than 10 ppm |
|
Iron |
Less than 5ppm |
Less than 10 ppm |
|
Chlorides |
Less than 0.03% |
Less than 0.5% |
|
Sulphates |
Less than 0.02% |
Less than 0.5% |
|
Packing |
As required |
As required |
GRADES AND SPECIFICATIONS OF SODIUM ACETATE ANHYDROUS POWDER.
|
SPECIFICATIONS |
SODIUM ACETATE ANHYDROUS PURE |
SODIUM ACETATE ANHYDROUS TECHNICAL |
|
Purity |
99 % minimum purity as CH3COONa |
98.5% minimum purity as CH3COONa |
|
Appearance |
Snow-White Powder |
White to Off-White Powder |
|
Clarity of 10% Solution |
A 10% Solution w/v is clear and colourless |
A 10% Solution w/v is clear |
|
pH (10% in water) |
pH between 7.5-9 |
pH between 7.5-9 |
|
Arsenic |
Arsenic < 1ppm. |
Arsenic < 1ppm. |
|
Calcium and Magnesium |
To pass the test 50 ppm |
To pass the test 100 ppm |
|
Heavy Metals |
Heavy Metals < 1ppm |
Heavy Metals < 10ppm |
|
Iron |
Iron < 5ppm |
Iron < 10ppm |
|
Chloride |
Chloride < 100ppm |
Chloride <0.5% |
|
Sulphate < 225ppm |
Sulphate < 20ppm |
Sulphate <0.5% |
|
Packing |
25kg(55 lbs)-50kg bags or pellets or as required |
|
We offer Sodium Acetate IP Sodium Acetate BP Sodium Acetate USP Sodium Acetate Ph. Eur. and Extra Pure from our world class FDA approved, ISO-9001-2008 Certified facility, Anmol Chemicals
Sodium Acetate IP Pharma Grade
|
Particulars |
IP Grade |
|
Dry Basis Assay |
99 to 101% |
|
Characteristics |
Colourless Crystals |
|
Solubility |
Soluble in 0.8 part of water and in 19 parts of Ethanol (96%) |
|
Clarity and colour of 10% w/v solution |
Clear and Colourless |
|
Alkalinity (pH of 5% solution) |
7.5-9.0 |
|
Arsenic |
2 ppm |
|
Calcium and Magnesium (calculated as Ca) |
50 ppm |
|
Heavy Metals as Lead |
10 ppm |
|
Iron |
10 ppm |
|
Chloride |
200 ppm |
|
Sulphate |
200 ppm |
|
Reducing Substances |
Passes test |
|
Packing |
In 50 Kg HDPE bag with HMHDPE liner |
Sodium Acetate USP Specifications
Sodium Acetate
USP
C2H3NaO2·3H2O 136.08
Assay
Sodium
Acetate contains three molecules of water of hydration, or is anhydrous. It
contains not less than 99.0 percent and not more than 101.0 percent of
C2H3NaO2, calculated on the dried basis.
Packaging and storage Preserve in tight containers.
Labeling
Label it
to indicate whether it is the trihydrate or is anhydrous. Where Sodium
Acetate is intended for use in hem dialysis, it is so labeled.
Identification A
solution responds to the test for Sodium and for Acetate.
pH: between 7.5 and
9.2, in a solution in carbon dioxide-free water containing the equivalent of
30 mg of anhydrous sodium acetate per mL.
Loss on drying Dry
at 120 to constant weight: the hydrous form loses between 38.0% and 41.0% of
its weight, and the anhydrous form loses not more than 1.0% of its weight.
Insoluble matter Dissolve the equivalent of 20 g of anhydrous sodium acetate in 150 mL of
water, heat to boiling, and digest in a covered beaker on a steam bath for 1
hour. Filter through a tarred filtering crucible, wash thoroughly, and dry at
105 : the weight of the residue does not exceed 10 mg (0.05%).
Chloride
A portion
equivalent to 1.0 g of anhydrous sodium acetate shows no more chloride than
corresponds to 0.50 mL of 0.020 N hydrochloric acid (0.035%).
Sulfate
A portion
equivalent to 10 g of anhydrous sodium acetate shows no more sulfate than
corresponds to 0.50 mL of 0.020 N sulfuric acid (0.005%).
Calcium and magnesium To 20 mL of a solution containing the equivalent of 10 mg of anhydrous
sodium acetate per mL add 2 mL each of 6 N ammonium hydroxide, ammonium
oxalate TS, and dibasic sodium phosphate TS: no turbidity is produced within
5 minutes.
Potassium
Dissolve
the equivalent of 3 g of anhydrous sodium acetate in 5 mL of water, add 1N
acetic acid drop wise until the solution is slightly acidic, and then add 5
drops of sodium cobalt nitrite TS: no precipitate is formed.
Aluminum: (where it
is labeled as intended for use in hem dialysis) the limit is 0.2΅ =g per g.
Heavy metalsthe
limit is 0.001%.
Organic volatile
impurities: meets the requirements.
For more contact
Sodium Acetate manufacturers at:
MUBY CHEMICALS
S-8, SARIFA MANSION, 2ND FLANK ROAD,
CHINCHBUNDER, MUMBAI 400009, INDIA
TEL: (OFFICE)
91-22-23770100, 23726950, 23774610, 23723564. FAX: 91-22-23728264
e-mail: info@mubychem.com
Cell Call
to Anmol: +91-9821870100
USA & Canadian Customers may Call
773-829-5811
Copyright
and Usual Disclaimer
is Applicable
Last updated:
06 January, 2012.
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University of Phase Change Material
ZnCl2 --- Ammonium Chloride --- Calcium Chloride --- Potassium Chloride --- Sodium Acetate
Ammonium Chloride --- Calcium Chloride --- Potassium Chloride --- Sodium Acetate
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