Mira Organics Private Limited

Chlorbutol I.P. is one of our most recognized chemical
compounds. We formulate them with eco-friendly procedures in the laboratory. We
also test our range on parameters such as solubility, pH value and other. The
assortment of this chemical compound has characters like:

Sr. No.	Tests	Limits
01.	Description	White Crystaline Powder White
02.	Solubility	Freely Soluable in Ethanol (95%) in ether in Chlorofrom & in Volatile Oils
03.	Identification	A-Test Basses B- Test Basses C - Test Basses D-Test Basses
04.	Appearance of Solution	Test Basses
05.	Acidity	Test Basses
06.	Chloride	500 PPM Max.
07.	Sulphate Ash	0.1% Max.
08.	Water	4.5 to 6%
09.	Assay (On Anhydrous Basis) Between 98% to 101%

Chlorobutanol Hemihydrate B.P. is used a preservative, sedative and hypnotic chemical in the pharmaceutical sector. We offer chlorobutanol hemihydrate and anhydrous forms meeting chemical standards like USP NF, BP and Ph.Eu. Some of the salient features are:

•    Pure
•    Effective
•    Accurate composition
•    Precise pH value

We
also offer another chemical composition of Chlorobutanol USP, which has been
largely used in the pharmaceutical industries for its antimicrobial properties.
It is being used as a preservative in eye and ear drops. And they are also
available in chlorobutanol hemihydrate and anhydrous forms meeting chemical
compositions like USP NF,
BP and Ph.Eu.

With
us lies the best assortment of ondansetron HCL BP/HCL, which are formulated
adhering to international quality standards. We also formulate the chemical
according to clients’ specification. Some of the characteristic of our
formulated ondansetron are as blow:

No.	Tests	Limits
CHARACTERS
1.	Description	White to off white powder
2.	Solubility	Sparingly soluble in water and in Alcohnti Solubd in Methanol, Sliahtly Soluble in MDC.
IDENTIFICATION
1.	Identification	A) IR The infra red absorption spectrum of iho test sample exhibits maxima only at the wavelengths as that of the working standard. |
		B) Chloride Test
TES'
1.	Impurity B (By TLC|	Not more Than 0.4%
2.	Related Substances (By HPLC)	Impurity C : NMT 0.2% Impurity D:NMT 0,1% Impurity E: NMT 0.2% Impurity E : NMT 0.2% Total total Imparities: NMT 0.4%
3.	Water	9.0 to 10.5%
4.	Sulphated Ash	NMT 0.1%
ASSAY
1.	Assay	Should be between 97.5% to 102% (Anhyd Basis) |

We
formulate and offer superior quality and compositionally accurate phenyl
propalonamine HCL BP/USP. Our white crystalline powder is soluble in water as
well as in ethyl alcohol and is tested for acidity and pH values before
delivering to our clients. Some of the specifications of our phenyl
propalonamine are given in the tabulated form below:
 

No	Tests	Limits
1.	Description	A White Crystalline Powder
2.	Solubility	Freely Soluble in Water and Ethyl Alcohol (96%), Practically in soluble in Methylene Chloride.
3.	Identification	A, Melting Point (2.2.14) 194°C.to 197°C. B, Infrared absorption Spectrum (2.2.24) C, Related Substance (2.2,24) D, Color Identification E, Chloride Test (if give reaction (a) of Chloride)
4.	Appearance of Solution	Solution S is Clear (2.2.1) and Colorless (Method II 2.2.2)
5.	Acidity of Alkalinity	As Per BP/USP
6.	Related Substances	AS Per BP/USP (2.2.27)
7.	Phenylpropanon	Absorption at 283 nm is not more than 0.10
8.	Heavy Metal	Not More Then 20 ppm.
9.	Loss on Drying	Not More then 0.5%
10.	Sulphated Ash	Note More Then 0.1%
11.	Assay (On Dry Basis)	Between 99.0% to 101.5%