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China Northwest Factory Manufacturer Cobamamide Cas 13870-90-1 For stock delivery

China Northwest Factory Manufacturer Cobamamide Cas 13870-90-1 For stock delivery

  • Purity
    99.9%
  • Use
    Health Care
  • Origin
    China
  • Package
    1KG/Tin 25KG/Drum*Carton
  • Manufacturer
    XI'AN LEADER BIOCHEMICAL ENGINEERING CO.,LTD
  • Place of Origin
    CHINA
  • Brand Name
    Leader
  • Certification
    ISO,GMP,SGS,HALA,KOSER,HACCP
  • Model Number
    LD
  • Minimum Order Quantity
    25KGS
  • Price
    Negotiate
  • Packaging Details
    25KG/Drum
  • Delivery Time
    2-3 working days
  • Payment Terms
    Western Union, MoneyGram, T/T, L/C
  • Supply Ability
    10MTS/Month

China Northwest Factory Manufacturer Cobamamide Cas 13870-90-1 For stock delivery

5'-Deoxyadenosylcobalamin Basic information
Product Name: 5'-Deoxyadenosylcobalamin
Synonyms: DIMETHYLBENZIMIDAZOLYLCOBAMIDE COENZYME, 5,6-;DMBC COENZYME;COENZYME B12;COBAMAMIDE;COBAMAMIDE/DIBENCOZIDE;COBAMIDE;5'-deoxyadenosylcobalamin;5'-DEOXYADENOSYLCOBALAMINE
CAS: 13870-90-1
MF: C72H100CoN18O17P
MW: 1579.58
EINECS: 237-627-6
Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;PHARMACEUTICALS
Mol File: 13870-90-1.mol
5'-Deoxyadenosylcobalamin Structure
 
5'-Deoxyadenosylcobalamin Chemical Properties
storage temp. 2-8°C
pka 3.5(at 25℃)
Water Solubility 26g/L(24 ºC)
Merck 13,2476
BRN 4122932
 
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
RTECS GG3800000
F 8
HS Code 2936260000
Toxicity LD50 oral in guinea pig: 5gm/kg
MSDS Information
Provider Language
SigmaAldrich English
 
5'-Deoxyadenosylcobalamin Usage And Synthesis
Originator Actimide,Tobishi
Uses emulsifying agent
Definition ChEBI: A member of the class of cobalamins that is vitamin B12 in which the cyano group is replaced by a 5'-deoxyadenos-5'-yl moiety. It is one of the two metabolically active form of vitamin B12.
Manufacturing Process Isopropylidine adenosine was converted to the p-toluene sulphonyl (tosyl) ester by reaction with tosyl chlorine solution, following the method of Clark et al. (1951) [J. Chem. Soc. 2952]. Because of its tendency to cyclization, the reagent was used directly it was ready. A reaction flask with separating funnels was set up in such a way that the whole system could be evacuated and filled with pure nitrogen two or three times, to eliminate all oxygen, and reagents could then be added when desired, in the closed system.
The flask contained 700.0 mg hydroxocobalamin in 20 ml of water, one funnel 200.0 mg sodium borohydride in 10 ml of water, and another the crude isopropylidine adenosine tosyl ester made from 500 mg isopropylidine adenosine dissolved in 10 ml of 50% aqueous methanol. On adding the borohydride to the vitamin, the color changed instantly from red to brown, then slowly to a greenish black. After 15 min the isopropylidine adenosine tosyl ester was added, and the colour slowly changed to a red-brown. After 45 min at room temperature air was admitted and the mixture was shaken to reoxidise any remaining reduced vitamin B12. The alkaline solution was neutralized with dilute hydrochloric acid and extracted with phenol carbon tetrachloride 3:1 in small portions till the aqueous layer was nearly colorless. The combined extracts were washed with water, mixed with about ten parts of carbon tetrachloride- 10:1 and shaken with small portions of water till all red color was removed.
The product was purified by chromatography on columns of DEAE (diethyl aminoethyl) cellulose (3 x 1) followed by CM (carboxymethyl) cellulose (6 x 1), developed with water. Nearly all the color washed quickly through DEAE cellulose. The effluent and washes were applied to the CM cellulose column, which was further developed with water. Elution was continued as long as this fraction continued to emerge, in a total of 850 ml. One half of this fraction (425 ml) was concentrated to a few ml under reduced pressure; it crystallized slowly after adding to slight turbidity. So cobamamide was obtained.
Therapeutic Function Anabolic, Analgesic
Agricultural Uses Cobamide enzyme is the cobalt complex formed between the cobalt-porphyrin ring structure and the nucleotide in vitamin B12 co-enzyme.