|
S.NO.
|
PROTOCOL
|
SPECIFICATION
|
RESULT
|
|
1
|
Description
|
White to Off-White powder
|
Complies
|
|
2
|
Identification
|
The IR spectrum of the IR spectrum of the Chondroitin Sulphate Sodium WS.
|
Complies
|
|
3
|
Clarity and Color
|
NMT 0.35 A
|
Complies
|
|
4
|
Specific optical Rotation, Deg.
|
-10.0 to -20.0
|
-15.21
|
|
5
|
PH, 1 gm/100 ml
|
5.5 â 7.5
|
6.31
|
|
6
|
Loss on drying, % W/W
|
NMT 10
|
6.72
|
|
7
|
Residue on lgnition, %W/W
|
20.0-30.0
|
26.49
|
|
8
|
Chloride, % W/W
|
NMT 0.5
|
Complies
|
|
9
|
Sulphate, % W/W
|
NMT 0.24
|
Complies
|
|
10
|
Proteins, % W/W
|
NMT 6.0
|
Complies
|
|
11
|
Heavy Metals, ppm
|
NMT 20
|
Complies
|
|
12
|
Organic volatile Impurities
|
It meets the requirements.
|
Complies
|
|
13
|
Assay (On dried basis), %W/W
|
NLT 90
|
99.30
|
|
14
|
Microbiological Report
|
|
a). Total Microbial Count, Cfu/g
|
NMT 1000
|
Complies
|
|
b).Yeast & Mould, Cfu/g
|
NMT 100
|
Complies
|
|
c).E-Coil & Salmonella, Cfu/g
|
Absent
|
Complies
|
|
|
|
|
|
The Sample Complies with the above said specification.
|