Yashica Pharmaceuticals Private Limited
Thane, Maharashtra
GST 27AAACY3217A1ZT
TrustSeal Verified
IndiaMART Verified Exporter
Approx. Rs 20,000 / Kg
Product Name | Ondensetron HCl BP/EP/USP |
Chemical Name | 1,2,3,9-Tetrahydro-9-Methyl-3-[(2-Methyl-1H-Imidazol-1-Yl)Methyl]-4H-Carbazol-4-One Monohydrochloride Dihydrate |
CAS Number | 103639-04-9 |
Chemical Formula | C18H19N3O • ClH • 2H2O |
Molecular Mass | 365.9 G/Mol |
Therapeutic Category | Antagonists |
Instructions of Ondensetron HCl :
Test | Specification |
Description | White To Off White Powder. |
Solubility | Sparingly Soluble In Water And In Alcohol, Soluble In Methanol, Slightly Soluble In MDC. |
Identification | A) IR : The Infra Red Absorption Spectrum Of The Test Sample Exhibits Maxima Only At The Same Wavelengths As That Of The Working Standard B) Chloride Test |
Impurity B (By TLC) | Impurity C : NMT 0.2% Impurity D : NMT 0.1% Impurity E : NMT 0.2% Impurity F : NMT 0.2% Total Impurities : NMT 0.4% |
Water | 9.0 To 10.5% |
Sulphated Ash | NMT 0.1% |
Assay | Should Be Between 97.5% To 102% (Anhydrous Basis) |
Approx. Rs 550 / Kg
Product Name | Dicyclomine Hydrochloride BP/EP/USP |
Chemical Name | [Bycyclohexyl]-1-Carboxylic Acid, 2-(Diethylamino) Ethyl Ester, Hydrochloride |
CAS Number | 67-92-5 |
Chemical Formula | C19H35NO2HCL |
Molecular Mass | 345.95 G/Mol |
Therapeutic Category | Antispasmodic |
Specification of Dicyclomine Hydrochloride :
Test | Specification |
Description | White Or Almost White Powder |
Solubility | Practically Insoluble In Water, Soluble In Dimethylformamide, Slightly Soluble In Alcohol In Methanol. |
Identification | A. Melting Point : 244oc To 248oc B. By IR C. By TLC |
Appearance Of Solution | Clear And Not Intensely Coloured Than Ref. Solution. |
Related Substances By HPLC | Individual Impurity: NMT 0.25% Total Impurity : NMT 0.5% |
Heavy Metals | Not More Than 20 PPM |
Sulphated Ash | Not More Than 0.1% |
Assay (On Dried Basis) | NLT 99% And NMT 101.0% |
Approx. Rs 5,000 / KG
Product Name | Fluconazole BP/EP/USP |
Chemical Name | 2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol |
CAS Number | 86386-73-4 |
Chemical Formula | C13H12F2N6O |
Molecular Mass | 306.27 g/mol |
Therapeutic Category | Antifungal |
Specification of Fluconazole :
Test | Specification |
Description | White or almost white crystalline powder |
Solubility | Freely soluble in methanol, soluble in alcohol and in acetone, sparingly soluble in isopropanol and in chloroform, slightly soluble in water, very slightly soluble in toluene. |
Appearance of solution | 5%w/v Solution in methanol should be clear and colorless |
Identification By IR test By UV test | Determine by infrared absorption spectrophotometry compare the spectrum with the obtained with fluconzole RS or with the reference spectrum of fluconzole. When examined in the range 200 nm to 350 nm, a 0.025%w/v solution in methanol shows absorption maxima at about 266nm and 261 nm |
Loss on Drying | NMT 0.50% |
Sulphated ash | NMT 0.10% |
Iron test | 20 ppm |
Related Compound by HPLC (TEST-1) | Impurity A : NMT 0.20% Impurity about RRT 0.6 : NMT 1.00 % Related Compound B : NMT 0.10 % Related Compound C : NMT 0.20 % Any single maximum Unknown Impurity : NMT 0.10 % Total unknown impurities : NMT 0.30 % Total Impurities : NMT 1.50 % |
Assay ( on Anhydrous basis ) | NLT 98.00% and NMT 102.00%w/w |
Residual Solvents - Methyl Chloride - Ethyl acetate - Toluene - Methanol - Acetone - Isopropyl alcohol - Benzene | NMT 500 ppm NMT 1000 ppm NMT 890 ppm NMT 1000 ppm NMT 1000 ppm NMT 1000 ppm NMT 2 ppm |
Approx. Rs 2,200 / KG
Product Name | Cetrimide BP/EP/USP |
Chemical Name | Hexadecyl(trimethyl)azanium bromide |
CAS Number | 9036-06-0 |
Chemical Formula | C19H42BrN |
Molecular Mass | 364.45 g/mol |
Therapeutic Category | Antiseptic |
Specification of Cetrimide :
Test | Specification |
Description | A white or almost white, valuminour, free flowing powder, odour faint and characteristic |
Solubility | Freely soluble in water, in ethanol (95%) and in chloroform,practically insoluble in ether |
Identification | To comply with BP standards |
Loss on drying | Not More Than 2.0 % ,determined on 1.0g by drying in an oven at 100°C to 105°C for 2 hrs. |
Sulphated ash | Not More Thanm0.5 %,determined on 1.0g |
Appearance of solution/clarity and colour of solution | 2 % solution in distilled water is clear |
Acidity or Alkalinity | Max :Limit 0.1MI of 0.1M HCI/0.1M NaOH Solution |
Amines and amine salts | To comply with BP standard |
Assay | Limit 96 % to 101 % |
Approx. Rs 2,200 / KG
Product Name | Desloratidine BP/EP/USP |
Chemical Name | 8-chloro-6,11-dihydro-11-(4-piperdinylidene)- 5H-benzo [5,6] cyclohepta[1,2-b]pyridine |
CAS Number | 100643-71-8 |
Chemical Formula | C19H19ClN2 |
Molecular Mass | 310.82 g/mol |
Therapeutic Category | Antihistamine |
Instructions of Desloratidine :
Test | Specification |
Description | A White to light brown colored crystalline powder |
Solubility | Freely soluble in methanol. |
Identification A) By IR | The IR spectrum of the sample recorded as KBr pellet is concordant with similarly recorded spectrum of working standard. |
Water content by KF | NMT 1.0% |
Melting range | Between 152oC to 159oC |
Heavy Metals | Not more than 20 ppm |
Sulphated Ash | Not more than 0.10% w/w |
Additional Test Residual solvents (By GC) | Single Max Impurity: N MT 0.10 % Total Impurities: NMT 0.30 % |
ssay (on anhydrous basis)A | Not less than 99.0% and NMT 101.0% |
Approx. Rs 15,000 / Kg
Product Name | Donepezil Hydrochloride BP/EP/USP |
Chemical Name | ( )-2-[(1-Benzyl-4-piperidy)methyl-5,6-dimethoxy-1-indanone, hydrochloride |
CAS Number | 120011-70-3 |
Chemical Formula | C24H29NO3.HCl |
Molecular Mass | 415.95 g/mol |
Therapeutic Category | - |
Specification of Donepezil Hydrochloride :
Test | Specification |
Description | White crystalline powder |
Solubility | Freely soluble in chloroform; soluble in water glacial acetic acid; slightly soluble in alcohol acetonitrile; practically insoluble in ethyl acetate n-hexane. |
Identification A) By Infrared Absorption B) By HPLC C) By Chlorides | To match with Working / Reference standard The retention time of the major peak of the sample solution corresponds to that of the standard solution, as obtained in the assay. To meet the test. |
Inorganic Impurities | A) Heavy Metals NMT 20ppm B) Residue on ignition NMT 0.1% w/w |
Specific Tests | Water content by KF NMT 0.4% w/w |
Organic Impurities By HPLC | Desbenzyl donepezil NMT 0.20% Hydroxydonepezil NMT 0.20% Donepezil related compound A NMT 0.10% Any individual unspecified impurity NMT 0.10% Total impurities NMT 1.0% |
Assay by HPLC (on anhydrous basis) | NLT 98.0% NMT 102% w/w |
Additinational Test Residual solvents by HS GC | Methanol NMT 3000ppm Isopropyl alcohol NMT 5000ppm Chloroform NMT 60ppm Methl Isobutyl Ketone NMT 5000ppm Toluene NMT 890ppm |
Approx. Rs 5,500 / KG
Product Name | Fluconazole BP/EP/USP |
Chemical Name | 2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol |
CAS Number | 86386-73-4 |
Chemical Formula | C13H12F2N6O |
Molecular Mass | 306.27 g/mol |
Therapeutic Category | Antifungal |
Specification of Fluconazole :
Test | Specification |
Description | White or almost white crystalline powder |
Solubility | Freely soluble in methanol, soluble in alcohol and in acetone, sparingly soluble in isopropanol and in chloroform, slightly soluble in water, very slightly soluble in toluene. |
Appearance of solution | 5%w/v Solution in methanol should be clear and colorless |
Identification By IR test By UV test | Determine by infrared absorption spectrophotometry compare the spectrum with the obtained with fluconzole RS or with the reference spectrum of fluconzole. When examined in the range 200 nm to 350 nm, a 0.025%w/v solution in methanol shows absorption maxima at about 266nm and 261 nm |
Loss on Drying | NMT 0.50% |
Sulphated ash | NMT 0.10% |
Iron test | 20 ppm |
Related Compound by HPLC (TEST-1) | Impurity A : NMT 0.20% Impurity about RRT 0.6 : NMT 1.00 % Related Compound B : NMT 0.10 % Related Compound C : NMT 0.20 % Any single maximum Unknown Impurity : NMT 0.10 % Total unknown impurities : NMT 0.30 % Total Impurities : NMT 1.50 % |
Assay ( on Anhydrous basis ) | NLT 98.00% and NMT 102.00%w/w |
Residual Solvents - Methyl Chloride - Ethyl acetate - Toluene - Methanol - Acetone - Isopropyl alcohol - Benzene | NMT 500 ppm NMT 1000 ppm NMT 890 ppm NMT 1000 ppm NMT 1000 ppm NMT 1000 ppm NMT 2 ppm |
Approx. Rs 15,000 / KG
Product Name | Nortriptyline Hydrochloride BP/EP/USP |
Chemical Name | 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,hydrochloride |
CAS Number | 894-71-3 |
Chemical Formula | C19H22ClN |
Molecular Mass | 294.84 g/mol |
Therapeutic Category | antidepressant |
Instructions of Nortriptyline Hydrochloride :
Test | Specification |
Appearance | A white or almost white powder |
solubility | Sparingly soluble in water, soluble in alcohol and in methylene chloride. |
Identification First Identification Second Identification | Infrared absorption Comparing with the spectrum (as KBr disk) obtained with Nortriptyline hydrochloride reference standard (working standard) Test for chlorides Should be positive for chloridesTest for chlorides Should be positive for chlorides A) Melting point (°c) Between 216 and 220 B) Specific Absorbance 465 to 495 at 239nm C) Chemical test A red colour develops slowly D) Test for chlorides Should be positive for chlorides |
Tests Appearance of the solution Acidity (or) Alkalinity Related substance (By TLC %) | The solution is clear and not more intensely coloured than reference solution B7 The solution is yellow The solution is red Dibenzosuberone NMT 0.05 Any other spot(other than Dibenzosuberone ) NMT 0.1 |
Heavy metals (ppm) | NMT 20 |
Loss on drying (%w/w) | NMT 0.5 |
Sulphated ash | NMT 0.1 |
Assay (By titrimetry, %, w/w, on dried basis) | NLT 98.0 and NMT the equivalent of 101.0 |
Approx. Rs 3,200 / KG
Product Name | Cetirizine Dihydrochloride BP/EP/USP |
Chemical Name | - |
CAS Number | 83881-52-1 |
Chemical Formula | C21H27Cl3N2O3 |
Molecular Mass | - |
Therapeutic Category | Antihistamine |
Instructions of Cetirizine Dihydrochloride :
Test | Specification |
Characteristics | White Crystalline powder |
Identification | A,B,C,D E as per B.P. |
Solubility | Soluble in water Methanol |
Melting Point | 210oc to 218oc |
pH | 1.2 to 1.8 |
Heavy Metals | Not more than 20 ppm |
Sulphated Ash | Not more than 0.2% |
Loss On Drying | Not more than 0.5% |
Related impurities [By TLC] | Spot of Ref. Material |
Assay On Dried Basis | Between NLT 99.0 % to NMT 100.5% |
Approx. Rs 50,000 / Kg
Product Name | Rosuvastatin Calcium BP/EP/USP |
Chemical Name | 7 - [4 - (4 - fluorophenyl) - 6 - (1 - methylethyl) - 2 - [methylsulfonyl)amino] - 5 - pyrimi - dinyl] - 3,5 - dihydroxy - 6 - heptenoic acid calcium |
CAS Number | 147098-20-2 |
Chemical Formula | 2C22H27FN3O6S • Ca |
Molecular Mass | 1001.14 g/mol |
Therapeutic Category | HMG-CoA Reductase Inhibitors |
Instructions of Rosuvastatin Calcium :
Test | Specification |
Description | A white to creamish colour powder. |
Solubility | Soluble in 100 parts of N,N-Dimethyl Formamide |
Identification a) By I.R. b)By HPLC | I.R. spectrum should be identical to that of standard Retention time of the sample peak should corresponds to that of standard |
Water by K.F. (in DMF) | NMT 8.0%w/w |
Calcium Content | 3.0% - 5.0%w/w |
Related Substances (by HPLC) a) Max. Single Impurity b) Total Impurities | NMT 1.0% NMT 2.0% |
Assay (HPLC,OAB) | NLT 97% w/w |
Approx. Rs 4,500 / Kg
Our organization holds expertise in providing superior grade Active Pharmaceutical Ingredient (API) to our customers.
Our offered API’S are widely appreciated by our customers, which are situated all round the world.
Known for its best quality, clients can avail this Active Pharmaceutical Ingredient (API) at industry leading prices from us.
Instructions:
Approx. Rs 8,500 / Kg
We are leading manufacturer and exporter of Olanzapine and our product is made up of good quality.
Olanzapine is a Yellow Crystalline Powder and an atypical antipsychotic. It is used for the treatment of schizophrenia and bipolar disorder.
NAME OF PRODUCT : Olanzapine | |
CAS NO | 132539-06-1 |
Chemical Formula | C17H20N4S |
MOL. WEIGHT | 312.439 G/Mol |
Approx. Rs 55,000 / KG
Approx. Rs 1.75 Lakh / KG
Approx. Rs 3,700 / Kg
TEST | SPECIFICATION |
Description | White, odorless, crystalline powder or small crystals. It melts at about 210ºC with decomposition. |
Solubility | Freely soluble in water, in formic acid, in methanol in chloroform. sparingly soluble in dehydrated alcohol: insoluble in ether. |
Identification A. IR spectrum B. HPLC C. Chlorides. |
To be concordant with USP To comply with USP To comply with USP |
Specific Rotation (at 25 ºC) | +110.0º to +116.0º |
Loss on Drying | NMT 0.50% w/w |
Residue on Ignition | NMT 0.10% w/w |
Heavy Metals | NMT 20 ppm |
Related Substances (By HPLC) | Desacetyl Diltiazem HCI NMT 0.30% Unknown Individual Impurity NMT 0.10% Total impurities including desacetyl Diltiazem HCI. NMT 0.50% |
Organic Volatile impurities (OVI) | Chloroform NMT 60ppm 1,4-Dioxane NMT 380ppm Methylene chloride NMT 600ppm Trichloro Ethylene NMT 80ppm |
Assay (on dry basis) | NLT 98.50% NMT 101.50% w/w of C22H26N2O4S.HCI |
Additional Test Residual Solvents | A. Toluene NMT 750 ppm B. Methanol NMT 500 ppm C. Isopropyl Alcohol NMT 1000 ppm D. Ethyl Acetate NMT 500 ppm |
Approx. Rs 150 / Pack
We offer a wide range of Pharmaceutical Pellets, which are exported all over the world.
These pellets are manufactured using fine quality chemicals. Our pellets are widely proffered for its efficiency.
These Pharmaceutical Pellets are manufactured under a strict inspection to ensure accuracy and quality.
The high quality and cost effectiveness of our range ensures that it is preferred by numerous clients across the market.
Instructions:
Approx. Rs 300 / Kg
Our organization holds expertise in providing superior grade Active Pharmaceutical Ingredient (API) to our customers.
Our offered API’S are widely appreciated by our customers, which are situated all round the world. Known for its best quality, clients can avail this Active Pharmaceutical Ingredient (API) at industry leading prices from us.
Specifications:
Approx. Rs 11,000 / Kg
Approx. Rs 650 / Kg
Approx. Rs 9,000 / KG
Product Name | Picosulfate Sodium BP/EP/USP |
Chemical Name | (2S,3aS,7aS)-1-[(2S)-2-{[(2S)-1-ethoxy-1-oxopentan-2-yl]amino}propanoyl]-octahydro-1H-indole-2-carboxylic acid |
CAS Number | 10040-45-6 |
Chemical Formula | C18H13NNa2O8S2 |
Molecular Mass | 481.41 g/mol |
Therapeutic Category | Antibacterial / steroidal anti-inflammatory |
Approx. Rs 8,000 / Kg
Product Name | Clopidogrel Bisulfate BP/EP/USP |
Chemical Name | (+)-(S)-methyl 2-(2-chlorophenyl)-2-(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate |
CAS Number | 113665-84-2 |
Chemical Formula | C16H16ClNO2S |
Molecular Mass | 321.82 g/mol |
Therapeutic Category | Antiplatelet |
Specification of Clopidogrel Bisulfate :
Test | Specification |
Description | White to off-white powder |
Solubility | Freely soluble in methanol |
Identification a) By IR b) Identification of RT by HPLC Assay method c) Sulphates | The IR spectrum of sample should be concordant with that of working standard. RT of principal peak in the sample Chromatogram should match that of standard Chromatogram. Should Respond to test for Sulphates |
Loss on drying (%, w/w) [ at 105°C for 2 hours] | NMT 0.50% |
Residue On Ignition | NMT 0.10% |
Related substances by HPLC | Impurity due to enantiometer A : NMT 0.20% Impurity due to enantiometer B : NMT 0.30% Impurity due to enantiometer C : NMT 1.00% Other Impurity : NMT 0.10% Total Impurity : NMT 1.50% |
Assay by HPLC on Dry basis (%w/w) | 97.00% - 101.50% |
Approx. Rs 1,600 / Kg
We are leading manufacturer and exporter of Caffeine and our product is made up of good quality.
We offer optimum quality Natural Caffeine to our valuable customers.
The offered extract is processed from green coffee bean, which is procured from well-known vendors.
This extract finds wide application in beverages, pharmaceuticals and foods processing industries.
Features:
Approx. Rs 800 / Kg
Meloxicam is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and fever reducer effects.
It is a derivative of oxicam, closely related to piroxicam, and falls in the enolic acid group of NSAIDs.
NAME OF PRODUCT : Meloxicam | |
CAS NO | 71125-38-7 |
Molar Mass | 351.403 G/Mol |
Bioavailability | 89% |
Protein Binding | 99.4% |
Approx. Rs 7,000 / PIECE
Product Name | Quinapyramine Chloride/Sulphate BP/EP/USP |
Chemical Name | - |
CAS Number | 23609-66-7 |
Chemical Formula | - |
Molecular Mass | g/mol |
Therapeutic Category | - |
Specification of Quinapyramine Chloride/Sulphate :
Test | Specification |
Description | A white, cream coloured or very pale yellow crystalline powder, odourless with a bitter taste |
Solubility | Soluble at 20°C in 2 parts of water almost in soluble in organic solvents. |
Identification | a). To 5 ml of a 1 % w/v solution in water add 1ml of potassium ferricyanide solution: a yellow precipitate is formed b). To 0.1gr add 0.2ml of fuming nitric acid. An immediate purple colour is produced c) It melts at about 266°C with decomposition d) Dissolve 0.1gr add 10 ml of water add 0.5ml of HCl, boil for 5 minutes cool and filter, the filtrate gives the reaction characteristic of sulphates. |
Acidity as pH | The pH of 10 % w/v solution in CO2 Free water it is not below 2.5 |
Arsenic | NMT 5 ppm |
Lead | NMT 10 ppm |
Loss on drying | NMT 1.5 % w/w determined by drying to constant weight at 130°C |
Sulphated ash | NMT 0.2 %w/w |
Assay | NLT 98.0 % w/w and NMT 102.0 % w/w calculated with reference to the substance dried under the prescribed conditions. |
Approx. Rs 350 / Kg
We are leading manufacturer and exporter of Ferrous Sulphate Pellets and our product is made up of good quality.
Ferrous sulfate is used to fortify foods and to treat iron-deficiency anemia.
PRESENTATION Ferrous Sulfate Pellets are available in 60%, 65%, 67.5%, 72%, 75%, 80% and 85% strengths. Ferrous Fumerate Pellets are available in 75% strength.
Customized strength of pellets also can be supplied as per the choice of the customers. These are in ready to fill form.
Approx. Rs 15,000 / kg
We are leading manufacturer and exporter of Procyclidine HCL BP and our product is made up of good quality.
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Product Name | Procyclidine HCL BP/EP/USP |
Chemical Name | 1-Pyrrolidinepropanol, A-Cyclohexyl-A-Phenyl-, Hydrochloride |
CAS Number | 1508-76-5 |
Chemical Formula | C28H29F2N3O |
Molecular Mass | 323.90 G/Mol |
Therapeutic Category | Anticholinergic Agent |
Specification of Procyclidine HCL :
Test | Specification |
Characteristics | White Crystalline Powder, Odorless Or Almost Odorless |
Solubility | Sparingly Soluble In Water, Soluble In Ethanol (96%) Practically Soluble In Acetone And Ether |
Identification | A. By IR B C (Chloride) |
Acidity | [ 4.5-6.5] |
Related Substances | Complies With Test Of BP |
Sulphated Ash | Limit: Not More Than 0.1 % |
Loss On Drying | Limit: Not More Than 0.5 % |
Assay | Limit: Between 98% To 101 % On Dried Basis |
Melting Point [I.H.S] | Limit: Between 221º C To 223ºC |
Approx. Rs 13,000 / Kg
Product Name | Residronate Sodium BP/EP/USP |
Chemical Name | 1-hydroxy-2-(3-pyridinyl)ethylidene]bis[phosphonic acid] |
CAS Number | 115436-72-1 |
Chemical Formula | C7H10NNaO7P2 |
Molecular Mass | 305.09 g/mol |
Therapeutic Category | Bisphosphonate |
Approx. Rs 4,000 / KG
Product Name | Amlodipine Base/Besylate BP/EP/USP |
Chemical Name | - |
CAS Number | 88150-42-9 |
Chemical Formula | C20H25ClN2O5 |
Molecular Mass | 408.88 g/mol |
Therapeutic Category | Antihypertensive |
Instructions of Amlodipine Base/Besylate :
Test | Specification |
Description | A white or almost white powder |
Solubility | Slightly soluble in water, freely soluble in methanol, sparingly soluble in ethanol, slightly soluble in 2-propanol |
Identification a) I.R b) U.V | The IR spectrum of sample is concordant with working standard spectrum. The solution shows absorption maximum at 360 nm. |
Optical Rotation | -0.1° to +0.1° |
Water content by KF | NMT 0.5 % w/w |
Sulphated Ash | NMT 0.2 % w/w |
Related substances (by HPLC) | Impurities D NMT 0.3 % All impurities other than impurity D NMT 0.3 % |
Assay (By HPLC on anhydrous basis) | NLT 97.0 % NMT 102.0 % w/w |
Related substances (by TLC ) | Total Impurities NMT 0.3 % Individual impurity NMT 0.1 % |
Description | A white or almost white powder |
Approx. Rs 15,000 / Kg
Product Name | Loratadine BP/EP/USP |
Chemical Name | Ethyl 4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylate |
CAS Number | 79794-75-5 |
Chemical Formula | C22H23ClN2O2 |
Molecular Mass | 382.88 g/mol |
Therapeutic Category | antidepressants |
Instructions of Loratadine :
Test | Specification |
Description | White off-white powder |
Solubility | Freely soluble in acetone, in chloroform, in methanol and in toluene, insoluble in water |
Identification A ) Infrared spectrum (In Mineral oil) B ) HPLC | The IR absorption spectrum of the preparation of the test specimen, exhibits maxima only at the same wavelengths as that of a similar preparation of the corresponding Loratadine working standard The retention time of the major peak in the chromatogram of the assay preparation corresponds to that in the chromatogram of the standard preparation as obtained in the assay |
Melting point (°C) | Between 132 and 137 |
Loss on drying (%, w/w) | NMT 0.5 |
Residue on ignition (%,w/w) | NMT 0.1 |
Heavy metals (%,w/w) | NMT 0.001 |
Related compounds (By HPLC) Related compounds A Related compounds B Each individual unknown impurity Total impurities | NMT 0.1 NMT 0.1 NMT 0.1 NMT 0.3 |
Assay By HPLC (%w/w) (On dried basis) | NLT 98.5 and NMT 101.0 |
Additional Tests Residual solvent/Organic volatile impurities (By GC with HSS,ppm) | Tetrahydrofuran : NMT 500 Toluene : NMT 500 Di-isopropyl ether : NMT 500 Triethylamine : NMT 50 |
Approx. Rs 1,800 / Kg
Product Name | Bromhexine Hydrochloride BP/EP/USP |
Chemical Name | N-(2-Amino-3,5-dibromobenzyl)-N-methylcyclohexanamine hydrochloride |
CAS Number | 611-75-6 |
Chemical Formula | C14H20Br2N2 HCL |
Molecular Mass | 412.59 g/mol |
Therapeutic Category | Antimucolytic |
Specification of Bromhexine Hydrochloride :
Test | Specification |
Characteristics | White crystalline powder |
Solubility | Alcohol : 100 to 1000 parts Methylene Dichloride : 100 to 1000 parts Water : 1000 to 10000 parts |
Identification | IR test : Complies with standard Thin Layer Chromatography : Complies with standard Chemical Test : Complies with test Primary Aromatic Amine Test : Complies with amine test Chloride test : Complies with chloride test |
Appearance of solution | Complies with test |
uv test | 208 to 211 nm |
Related substance (HPLC) | Identified impurity : Impurity A : NMT 0.1 % Impurity B : NMT 0.1 % Impurity C : NMT 0.1 % Impurity D : NMT 0.1 % Impurity E : NMT 0.1 % Unknown impurity : Impurity 1 : NMT 0.1 % Impurity 1 : NMT 0.1 % Total impurities : Not More Than 0.3 % |
Residual solvents | Alcohol : NMT 5000 ppm Toluene : NMT 890 ppm |
Foreign particles | Not detected |
Loss on drying | Not More Than : 1.0 % |
Approx. Rs 13,000 / Kg
Product Name | Residronate Sodium BP/EP/USP |
Chemical Name | 1-Hydroxy-2-(3-Pyridinyl)Ethylidene]Bis[Phosphonic Acid] |
CAS Number | 115436-72-1 |
Chemical Formula | C7H10NNaO7P2 |
Molecular Mass | 305.09 G/Mol |
Therapeutic Category | Bisphosphonate |
Approx. Rs 12,500 / Kg
Approx. Rs 6,000 / KG
Product Name | Haloperidol BP/EP/USP |
Chemical Name | 4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidyl]-1-(4-fluorophenyl)-butan-1-one |
CAS Number | 52-86-8 |
Chemical Formula | C21H23ClFNO2 |
Molecular Mass | 375.9 g/mol |
Therapeutic Category | antipsychotic |
Specification of Haloperidol :
Test | Specification |
Description | A white or almost white powder. |
Solubility | Practically insoluble in water, soluble in alcohol, in methanol in methylene chloride. |
First Identification B) IR E) Chloride test | The IR spectrum of sample should match with that of standard. A curdy, white precipitate is produced |
Second Identification A) Melting Range C) TLC D) Chemical Test E) Test for chloride | Between 150 ºC 153ºC Position size of principal spot obtained with sample shall be similar with that of standard. A violet colour is produced and becomes brownish red after 20 min A curdy, white precipitate is produced. |
Appearance of solution | The solution is clear and not more intensely coloured than reference solution Y7 |
Related substances by HPLC | Individual impurity : NMT 0.5% Total impurities : NMT 1.0% |
Heavy metals | NMT 20 ppm |
Loss on drying | NMT 0.5% |
Sulphated Ash | NMT 0.1% |
Assay (on dried basis) | NLT 99% and NMT 101% |
Approx. Rs 1,700 / Kg
Product Name | Progunil HCL BP/EP/USP |
Chemical Name | 1-(4-chlorophenyl)-5-isopropyl-biguanide hydrochloride |
CAS Number | 637-32-1 |
Chemical Formula | C11H17Cl2N5 |
Molecular Mass | 290.19 g/mol |
Therapeutic Category | Antimalarial |
Specification of Progunil :
Test | Specification |
Description | White crystalline powder, odorless. |
Solubility | Practically insoluble in chloroform and ether, slightly soluble in water soluble in ethanol |
Identification | Test A,B,C D should be comply |
Acidity or Alkalinity | NMT 0.2% |
Sulphated Ash | NMT 0.1% w/w |
4-Chloro Aniline | NMT 250 PPM |
Loss on drying @ 105oC for 3 hrs | NMT 0.5% w/w |
Related Substances By HPLC | 1. Single Impurity : NMT 0.7% 2. Total Impurity : NMT 1.0% |
Assay | NLT 98.5% w/w and NMT equivalent of 101.0% w/w of C11H16CLN5, HCL calculated with references to the dried substances |
Approx. Rs 6,500 / KG
We are leading manufacturer and exporter of Etoricoxib Intermediate and our product is made up of good quality.
Etoricoxib is a COX-2 selective inhibitor.
Current therapeutic indications are: treatment of rheumatoid arthritis, psoriatic arthritis, osteoarthritis, ankylosing spondylitis, chronic low back pain, acute pain and gout.
Approx. Rs 7,500 / Kg
NAME OF PRODUCT : Pantoprazole | |
TEST | STANDARDS |
Description | White To Off White Powder. |
Solubility | Freely Soluble In Water, Methanol In Dehydrated Alcohol; Practically Insoluble In Hexane In Dichloride Methane. |
Identification A) Infrared Absorption B) By HPLC C) Test For Sodium | The Infrered Absorption Spectrum Is Concordant With The Spectrum Obtained From Pantoprazole Sodium Working Standard. The Retention Time Of The Major Peak In The Chromatogram Of The Assay Preparation Correaponds To That In The Chromatogram Of The Standard Preparation As Obtained In The Assay A Dense Precipitate Is Formed Sodium Compounds Impart An Intense Yellow Color |
Water Content (By KF,% W/W) | Between 5.0 8.0 |
Heavy Metals (% W/W) | NMT 0.002 |
Related Compounds (By HPLC, % W/W) Related Compound A Related Compound B Related Compound C Related Compound D F Related Compound E Individual Impurity Total Impurities | NMT 0.20 NMT 0.15 NMT 0.10 NMT 0.20 NMT 0.10 NMT 0.10 NMT 0.5 |
Approx. Rs 75,000 / Kg
Approx. Rs 12,000 / Kg
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Sanjay Totre
(Managing Director)
Yashica Pharmaceuticals Private Limited
Syndicate, Thane,
Maharashtra,
India