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Thiamine Chloride Vitamin B1 Nutritional Supplements Vitamins And Derivatives Vitamin Ingredients CA
Thiamine Chloride Vitamin B1 Nutritional Supplements Vitamins And Derivatives Vitamin Ingredients CA

Thiamine Chloride Vitamin B1 Nutritional Supplements Vitamins And Derivatives Vitamin Ingredients CA

Thiamine Chloride Vitamin B1 Nutritional Supplements Vitamins And Derivatives Vitamin Ingredients

CAS No.:  67-03-8

Purity: ≥98%

Molecular weight:  337.27 g/mol

Molecular formula: C12H17ClN4OS·HCl

Appearance:White to white crystalline powder

Package:  1g10g100g1000g


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Thiamine Chloride Vitamin B1 Nutritional Supplements Vitamins And Derivatives Vitamin Ingredients CA

Thiamine Chloride Vitamin B1 Nutritional Supplements Vitamins And Derivatives Vitamin Ingredients CA

  • Originator:Sopharma

  • MF:C12H17ClN4OS·HCl

  • Purity:99%

  • Package:25kg/drum

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Product Details
Originator:
Sopharma
MF:
C12H17ClN4OS·HCl
Purity:
99%
Package:
25kg/drum
Color:
White Crystalline
Form:
Powder
Density:
1.3175 (rough Estimate)
Highlight: 

Thiamine Chloride vitamin b1

,

vitamin b1 99%

,67-03-8
Payment & Shipping Terms
Minimum Order Quantity
25kg
Price
USD
Packaging Details
drum   50cm✖60cm  fiber drum  or ziplock bag
Delivery Time
4-8 days
Payment Terms
L/C, T/T, Western Union
Supply Ability
1ton/per month
Product Description

Thiamine chloride VitaminB1 Nutritional Supplements Vitamins and Derivatives;Vitamin Ingredients;

Chemical Formula:

20230525160751_75087.png

Basic Parameters:

MW337.27
Melting point248 °C (decomp)
Storage tempKeep in dark place,Inert atmosphere,Room temperature
SolubilityDMSO : 6 mg/mL (19.95 mM)
Purity99%

Uses:

Vitamin B1 is used in method for cultivating tremella strain. Also, it is protein compound liquid comprising collagen and Rhodiola rosea extract or preparing injection to remove skin wrinkle.

Manufacturing Process:

2 Methods of preparation of thiamine:

1. 3-Ethoxypropionitrile reacted with diethoxymethoxy-ethane and 3-ethoxy- 2-methoxymethylenpropionitrile was obtained.

Then to the 3-ethoxy-2-methoxymethylenpropionitrile acetamidine was added and reaction mixture was stirred to give 4-amino-5-ethoxy-methyl-2- methylpyrimidine.

The 4-amino-5-ethoxy-methyl-2-methylpyrimidine was treated by hydrobromic acid to afford 4-amino-5-bromomethyl-2-methylpyrimidine hydrobromide.

The 4-amino-5-bromomethyl-2-methylpyrimidine hydrobromide reacted with 5-(2-hydroxyethyl)-4-methylthiazole in the presence of hydrobromic acid and as the result thiaminbromide was produced. For changing of the thiaminbromide to the thiamincloride the thiaminbromide was treated by AgCl.

2. To diethoxymethoxy-ethane malononitrile was added and ethoxymethylenmalononitrile was obtained. The ethoxymethylen-malononitrile reacted with acetamidine as a result 4-amino-5-cyano-2-methylpyrimidine was produced, which was reduced by H2/Raney-Ni to 4-amino-5-aminomethyl-2- methylpyrimidine.

To the 4-amino-5-aminomethyl-2-methylpyrimidine 1-acetoxy-3-chloropentan- 4-one was added in the presence CS2 and NH3, and reaction mixture was stirred, then to this mixture hydrochloric acid was added and thiamin (base) was obtained.

To thiamin (base) H2O2 and hydrocloricum acid are added, in the result reaction the thiamine chloride was obtained.


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