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Hebei Nengqian Chemical Import and Export Co., LTD

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Hebei Nengqian Chemical Import and Export Co., LTD

Country: China (Mainland)

Business Type:Trading Company

Ms.Winnie

Tel: +86 18233902561

Mobile: +86 18233902561

Tel: +86 18233902561

Fax: 4001020630

URL: https://www.nengqianchemical.com/

Province/state: Hebei

City: Handan

Street: Congtai District, La Defense North

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Thalidomide50-35-1

CAS NO.50-35-1

  • FOB Price: USD: 15.00-50.00 /Metric Ton Get Latest Price
  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,D/A,D/P,T/T
  • Available Specifications:

    medical grade(1-50)Metric Tonmedical grade(50-500)Metric Ton

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Product Details

Keywords

  • Phthalimide,N-(2,6-dioxo-3-piperidyl)- (6CI,7CI,8CI)
  • 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)isoindoline
  • 3-PHTHALIMIDOGLUTARIMIDE

Quick Details

  • ProName: Thalidomide50-35-1
  • CasNo: 50-35-1
  • Molecular Formula: C13H10N2O4
  • Appearance: white Powder
  • Application: Uses Adenos-2-thione is used as a phar...
  • DeliveryTime: 5-7 woking day
  • PackAge: 5mg/vial, 10 vials per box
  • Port: Qingdao port, Tianjin port
  • ProductionCapacity: 3000 Kilogram/Month
  • Purity: >99%
  • Storage: Sealed in dry,2-8°C
  • Transportation: According to demand
  • LimitNum: 1 Kilogram
  • packing: According to your request

Superiority

Our Advantage 

Rich Experience 
Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. 

Quality service 
Company cooperates with research institutes. We strictly control the process of raw materials up to finished product. 
  
24 hour service 
Quick and clear response to customers questions. Warm after sale service, we will help to solve the problems in your usage. 

High quality 
Dedicated to serving customers first, we provide reasonable prices, high quality products. 

Details

Name thalidomide
Synonyms thalidomide
THALIDOMIDE
N-PHTHALOLYLGLUTAMIMIDE
α-Phthalimidoglutarimide
3-PHTHALIMIDOGLUTARIMIDE
2-phthalimidoglutarimide
N-(2,6-DIOXO-3-PIPERIDINYL)PHTHALIMIDE
2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione
2-(2,6-dioxo-3-piperidinyl)-1h-isoindole-1,3(2h)-dione
CAS 50-35-1
731-40-8
EINECS 200-031-1
InChI InChI=1/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)
InChIKey UEJJHQNACJXSKW-UHFFFAOYSA-N

50-35-1 - Physico-chemical Properties

Molecular Formula C13H10N2O4
Molar Mass 258.23
Density 1.2944 (rough estimate)
Melting Point 269-271°C
Boling Point 401.48°C (rough estimate)
Flash Point 262.1°C
Water Solubility <0.1 g/100 mL at 22 ºC
Solubility 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.6mg/mL
Vapor Presure 1.65E-10mmHg at 25°C
Appearance White solid
Color white
Maximum wavelength(λmax) ['300nm(lit.)']
Merck 14,9255
pKa 10.70±0.40(Predicted)
Storage Condition Keep in dark place,Sealed in dry,Room Temperature
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
Refractive Index 1.5300 (estimate)
Physical and Chemical Properties Melting point 269-271°C
water-soluble <0.1g/100 mL at 22°C
Use Sedatives, for various types of leprosy reactions such as Fever, erythema nodosum, neuralgia, Arthralgia, Lymph Node Tumefaction, etc. have a certain effect, no therapeutic effect on leprosy
In vitro study Thalidomide must be metabolized by the liver to form epoxides, which may be the active teratogenic metabolite. Thalidomide selectively inhibits the production of tumor necrosis factor alpha (TNF-α) by human monocytes stimulated by lipopolysaccharide and other agonists. Thalidomide exerts its inhibitory effect on tumor necrosis factor alpha by enhancing mRNA degradation. Thalidomide acts directly on MM cell lines and MM cells of patients resistant to melphalan, doxorubicin and dexamethasone by inducing apoptosis and G1 phase growth arrest. Thalidomide enhances the anti-MM activity of Semetasone, whereas interleukin-6 inhibits its activity. Thalidomide is a potent co-stimulatory molecule for primary human T cells in vitro to synergistically increase interleukin-2 mediated T cell proliferation and interferon gamma production via the T cell receptor complex. Thalidomide also increases primary CD8 cytotoxic T cell responses induced by allogeneic dendritic cells in the absence of CD4 T cells.
In vivo study Thalidomide(200 mg/kg) caused inhibition of vascularized corneal regions in rabbits, with inhibition rates ranging from 30% to 51% in three experiments, with a median inhibition rate of 36%.

50-35-1 - Risk and Safety

Hazard Symbols T - Toxic
Toxic
Risk Codes R46 - May cause heritable genetic damage
R61 - May cause harm to the unborn child
R21 - Harmful in contact with skin
R25 - Toxic if swallowed
R62 - Possible risk of impaired fertility
R22 - Harmful if swallowed
Safety Description S53 - Avoid exposure - obtain special instructions before use.
S22 - Do not breathe dust.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs UN 2811 6.1/PG 3
WGK Germany 3
RTECS TI4375000
HS Code 29337900
Hazard Class 6.1(b)
Packing Group III
Toxicity LD50 oral in mouse: 2gm/kg

50-35-1 - Standard

Authoritative Data Verified Data

This product is (±)-N-(2, 6-dioxo-3-piperidinyl)-phthalimide. The content of C13H10N204 shall be 98.0% ~ 102.0% calculated as dry product.

 

50-35-1 - Trait

Authoritative Data Verified Data

  • This product is white to off-white powder; Odorless.
  • This product is dissolved in N,N-dimethylformamide or pyridine, very slightly dissolved in water, methyl spirit or ethanol, insoluble in ether and chloroform.

 

50-35-1 - Differential diagnosis

Authoritative Data Verified Data

  1. take about 0.1g of this product, put it in a test tube, add 10ml of sodium hydroxide solution, heat to boiling, that is, produce ammonia odor, let it cool, add ninhydrin lOmg, and the surrounding area of indene is blue.
  2. The infrared absorption spectrum of this product should be consistent with that of the reference product (General rule 0402).

 

50-35-1 - Exam

Authoritative Data Verified Data

Related substances

take about 0.lg of this product, weigh it accurately, put it in a 50ml measuring flask, add an appropriate amount of acetonitrile-water-phosphoric acid (50:50:0.1), ultrasonic to dissolve and dilute to the scale, shake well, take 10ml accurately, put it in a 100ml measuring flask, add 10ml of phosphoric acid solution (1-100), dilute it to scale with water, shake well, and use it as a test solution, add acetonitrile to dissolve and dilute to prepare a solution containing 1 mg per 1 ml as solution (1); Take an appropriate amount of phthalic acid reference substance, weigh it accurately, and use acetonitrile-water (80:5). Dissolve and quantitatively dilute to make a solution containing 1 mg per 1 ml, take an appropriate amount with precision, and quantitatively dilute with acetonitrile to make a solution containing 0 mg per 1 ml. 1 mg of the solution, as solution (2); Precision measure the solution (1), (2) each 2ml, put the same 100ml measuring flask, with acetonitrile-water-phosphoric acid (50:50:0.1) dilute to the scale, shake well, take 10ml accurately, put it in a 100ml measuring flask, add 10ml of phosphoric acid solution (1-100), dilute to the scale with water, shake well, as a control solution. According to the test of high performance liquid chromatography (General rule 0512), silica gel bonded with eighteen alkyl silane was used as the filler (×, 4um or equivalent column); Acetonitrile-water-phosphoric acid (5:95:0.1) as mobile phase A, acetonitrile-water-phosphoric acid (15:85:0.1) as mobile phase B; Flow rate was 2ml per minute; Gradient elution was carried out according to the following table; Detection wavelength was 218nm. Take the reference solution 200 u1, inject human liquid chromatograph, adjust the flow rate, so that the retention time of thalidomide peak is about 14 minutes; The relative retention time of phthalic acid peak and thalidomide peak is about 0.3. Take 200 u1 of the test solution and the reference solution respectively, inject the human liquid chromatograph and record the chromatogram. In the chromatogram of the test solution, if there are impurity peaks, the area of the phthalic acid peak shall be calculated according to the external standard method, and the single impurity shall not exceed 0.1%, and the total amount of the impurity shall not exceed 0.3%.

residual solvent

take 0.lg of this product, precision weighing, put it in 10ml measuring flask, add dimethyl sulfoxide to dissolve and dilute to the scale, shake, as a test solution; Take an appropriate amount of N,N-dimethylformamide, precision weighing, quantitative dilution with dimethyl sulfoxide to make a solution containing 8.8ug per 1 ml, shake, as a reference solution. According to the test of residual solvent determination (General 0861 third method), polyethylene glycol (PEG-20M) is used as stationary liquid; The initial temperature is 50°C, the temperature is maintained for 3 minutes, and the temperature is raised to 200°C at a rate of 20°C per minute, it was maintained for 7 minutes; The inlet temperature was 250°C; The detector temperature was 280°C. The sample solution and the reference solution were respectively 1 u1 and injected into the gas chromatograph. According to the external standard method to calculate the peak area, N,N-dimethylformamide residues should comply with the provisions.

loss on drying

take this product and dry it at 105°C for 4 hours, and the weight loss shall not exceed 0.5% (General rule 0831).

ignition residue

take l.Og of this product and check it according to law (General rule 0841). The residue left shall not exceed 0.3%.

Heavy metals

The residue left under the item of ignition residue shall not contain more than 20 parts per million of heavy metal when examined by law (General rule 0821).

 

50-35-1 - Content determination

Authoritative Data Verified Data

measured by high performance liquid chromatography (General 0512).

chromatographic conditions and system suitability test

silica gel bonded with eighteen alkyl silane was used as the filler; Acetonitrile-water-phosphoric acid (15:85:0.1) was used as the mobile phase; The detection wavelength was 237nm. The number of theoretical plates shall not be less than 7000 based on the thalidomide peak.

assay

take about 0.1kg of this product, weigh it accurately, put it in a 100ml measuring flask, add 80ml of acetonitrile, dissolve it by ultrasound, let it cool, dilute it to the scale with acetonitrile, shake it well, take 10ml accurately, put it in a 100ml measuring flask, add 10ml of phosphoric acid solution (1-100), dilute with water to the scale, and shake well. 20 u1 was accurately measured, and human liquid chromatography was injected, and the chromatogram was recorded. Another thalidomide reference substance was taken, and the same method was used for determination. According to the external standard method to calculate the peak area, that is.

 

50-35-1 - Category

Authoritative Data Verified Data

immunomodulatory drugs.

 

50-35-1 - Storage

Authoritative Data Verified Data

sealed storage.

 

50-35-1 - Thalidomide tablets

Authoritative Data Verified Data

This product contains thalidomide (C13H10N204) should be 93.0% to 107.0% of the label.

trait

This product is white or off-white.

identification

  1. take an appropriate amount of the fine powder of this product (about 0.lg of thalidomide), and show the same reaction according to the identification (1) Test under thalidomide.
  2. in the chromatogram recorded under the content determination item, the retention time of the main peak of the test solution should be consistent with the retention time of the main peak of the reference solution.

examination

  • Related substances take an appropriate amount of this product's fine powder (about 0.lg equivalent to thalidomide), weigh it accurately, put it in a 50ml measuring flask, and add an appropriate amount of acetonitrile-water-phosphoric acid (50:50: 0.1), ultrasonic dissolution and dilution of thalidomide to the scale, shake well, filter, precise amount of filtrate 10ml, put 100ml flask, add 10ml phosphoric acid solution (1-100), dilute to the scale with water, as a test solution. The determination was carried out according to the method for related substances of thalidomide. In the chromatogram of the test solution, if there are impurity peaks, the phthalic acid peak area shall be calculated according to the external standard method, and the single impurity shall not exceed 0.1% of the label amount and the total impurity shall not exceed 0.3% of the label amount.
  • the dissolution of this product, according to the dissolution and release determination method (General 0931 second method), with polyoxyethylene lauryl ether solution [take 5% polyoxyethylene lauryl ether solution 2.5ml, add hydrochloric acid solution (2-100) diluted to 1000ml] as the dissolution medium, the rotation speed is 75 rpm, operate according to law, after 60 minutes, take the solution filtration, continue filtrate as test solution. Take an appropriate amount of thalidomide reference substance, weigh it precisely, dissolve it with acetonitrile and dilute it quantitatively to make a solution containing 0.25mg(25mg specification) or 0.5mg(50mg specification) per 1 ml, take 10ml accurately, put in a 100ml measuring flask, Add 10ml of phosphoric acid solution (1-100), dilute with water to the scale, shake well, and use as a reference solution. According to the method under the content determination item, the dissolution amount of each tablet was calculated by the peak area according to the external standard method. The limit is 70% of the labeled amount and shall be in accordance with the provisions.
  • others shall be in accordance with the relevant provisions under the item of tablets (General rule 0101).

Content determination

Take 20 tablets of this product, precision weighing, fine grinding, precision weighing appropriate amount (about equivalent to thalidomide O.lg ), put it in a 100ml measuring flask, add 80ml of acetonitrile, sonicate thalidomide to dissolve, let it cool, dilute with acetonitrile to the scale, shake well, filter, take 10ml of continued filtrate with precision, put it in a 100ml measuring flask, Add 10ml of phosphoric acid solution (1-100), dilute it to the scale with water, shake it well, and use it as a test solution, and measure it according to the method under the thalidomide content determination item.

category

Same as thalidomide.

specification

(l)25mg (2)50mg

storage

light shielding, sealed storage.

Our company specializes in processing and selling chemical raw materials, chemical products, pharmaceutical intermediates, veterinary medicine intermediates, dye intermediates, pigments, cosmetics raw materials and chemical reagents,  

Our company has a number of sales team, service and information feedback vertical integration of a sound marketing network, products are sold throughout the country and exported to South Asia, Europe, America, Africa and other more than 20 countries and regions.  

Companies adhering to the "pursuit of quality, innovation and development" business philosophy, to serve as a foundation, for the survival by the quality, seek development by science and technology, adhere to quilty comes first,fair price,good sense of customer service and responsibility. in the future hebei Nengqian import and export trade Co.,Ltd will always hold "integrity, innovation" business philosophy, to achieve honesty management, on the way of specialization, internationalization,  Keep moving!  

Superiority
As a reliable partner for Chinese market, we are specialized in chemical raw materials; consolidate sourcing, marketing, sales, distribution and after-sale services, providing our partners with sourcing evaluation, technology supports, toll/contract manufacture, investment solution and suitable partnership establishment in China.
Service we can provide:
1. provide costomers with "one-stop"packaging service,from manufacture ,research,development,production,export and so on
2. Quality control, before shipment.
3. Prompt shipment with professional documents
4. Packing as your request, with photo before shipment
5.Mix and different products in ONE PCL,increase the working efficiency for customers.
6.We can export from many China main ports,convenient for the customes provide logistics services.
Our advantages: 

1, High quality with competitive price:

1) Standard:BP/USP/EP/Enterprise standard

2) All Purity≥99%

3) We are manufacturer and can provide high quality products with factory price.

 2, Fast and safe delivery

1) Parcel can be sent out in 24 hours after payment.Tracking number available

2) Secure and discreet shipment.Various transportation methods for your choice.

3) Customs pass rate ≥99%

4) We have our own agent/remailer/distributor who can help us ship our products very fast and safe,

and we have stock in there for transferring.

Product Packaging

1) 1kg/bag (1kg net weight, 1.1kg gross weight, packed in an aluminum foil bag)

2) 25kg/drum (25kg net weight, 28kg gross weight; Packed in a cardboard-drum with two plastic-bags inside; Drum Size: 510mm high, 360mm diameter)

 Storage

Stored in a cool and dry well-closed container. Keep away from moisture and strong light/heat.

Delivery

Usually within3-5 working days after full payment.

transport

EMS,DHL, TNT, UPS ,FEDEX, BY AIR, BY SEA

DHL Express, FedEx and EMS for quantity less than 50KG, usually called as DDU service; 

Sea shipping for quantity over 500KG; And air shipping is available for 50KG above;

For high value products, please select air shipping and DHL express for safe;

Our Service:
1. Fast Delivery: We can delivery within 24 hours upon receipt of your payment.
2. Quality can be promised. Hot sell to Worldwide.
3. Payment Terms: T/T,, t/t
4. Free Sample available at any time.
5. Tracking your order at any time. Inform your order's further new situation at any time.
6. Package: Professional packing with professional materials.

FAQ: 
1.Are you a trade company or factory   
We are a  factory with our own trading company.  

2.How do you control the quality   
Our factory is equipped with professional technicians to control quality, out inspectors take sample for testing every 2 hours to ensure the quality of our production. We also accept BV, SGS or any other Third-party inspection.   

3.How long is lead time  
We deliver goods within 3 days for small order, 7-10 days for bulk order.   

4. Where is your factory located How can I visit the factory   
 Our factory located in HEBEI, China.

5.Can i get some samples 
  Yes, we can supply free sample, but the shipping cost be paid by our customers. 

6.How to start orders or make payments 
  Proforma invoice will be sent first after confirmation of order, enclosed our bank information.Payment by T/T,  

7. How to confirm the Product Quality before placing orders 
  You can get free samples for some products,you only need to pay the shipping cost or arrange a courier to us and take the samples. 
8. How long is lead time

We deliver goods within 3 days for small order, 7-10 days for bulk order.

9.How do you treat quality complaint

First of all, our quality control will reduce the quality problem to near zero. If there is a realquality problem caused by us, we will send you free goods for replacement or refund your loss.