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CAS 15671-27-9

:

Sulfitocobalamin

Description:
Sulfitocobalamin, with the CAS number 15671-27-9, is a derivative of vitamin B12, specifically a form of cobalamin that contains a sulfonate group. It is characterized by its complex cobalt-centered structure, which is essential for its biological activity. This compound is typically a reddish-purple crystalline solid, reflecting the characteristic color of cobalamin derivatives. Sulfitocobalamin is soluble in water, which facilitates its use in various biochemical applications, particularly in the treatment of vitamin B12 deficiency. Its stability can be influenced by factors such as pH and light exposure, making proper storage conditions crucial. In biological systems, sulfitocobalamin can participate in enzymatic reactions, contributing to processes like DNA synthesis and red blood cell formation. Additionally, it may serve as a source of bioavailable cobalt, which is vital for numerous enzymatic functions. Overall, sulfitocobalamin plays a significant role in nutrition and biochemistry, particularly in relation to cellular metabolism and energy production.
Formula:C62H89CoN13O17PS
InChI:InChI=1S/C62H90N13O14P.Co.H2O3S/c1-29-20-39-40(21-30(29)2)75(28-70-39)57-52(84)53(41(27-76)87-57)89-90(85,86)88-31(3)26-69-49(83)18-19-59(8)37(22-46(66)80)56-62(11)61(10,25-48(68)82)36(14-17-45(65)79)51(74-62)33(5)55-60(9,24-47(67)81)34(12-15-43(63)77)38(71-55)23-42-58(6,7)35(13-16-44(64)78)50(72-42)32(4)54(59)73-56;;1-4(2)3/h20-21,23,28,31,34-37,41,52-53,56-57,76,84H,12-19,22,24-27H2,1-11H3,(H15,63,64,65,66,67,68,69,71,72,73,74,77,78,79,80,81,82,83,85,86);;(H2,1,2,3)/q;+3;/p-3
InChI key:InChIKey=IUJJHFFFUXMHFY-UHFFFAOYSA-K
SMILES:[O-](S(=O)O)[Co+3]1234[N]=5C6(C)C7[N-]1C(C(C)(C7CC(N)=O)CCC(=O)NCC(C)OP(=O)([O-])OC8C(O)C(N9C=[N]2C=%10C9=CC(C)=C(C)C%10)OC8CO)=C(C)C%11=[N]3C(=CC%12=[N]4C(=C(C)C5C(CCC(N)=O)C6(CC(N)=O)C)C(CC(N)=O)(C)C%12CCC(N)=O)C(C)(C)C%11CCC(N)=O
Synonyms:
  • Cobalamin, sulfito-
  • Cobalaminsulfonic acid
  • Cobinamide, Co-(sulfito-κO)-, dihydrogen phosphate (ester), inner salt, 3′-ester with (5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosyl-1H-benzimidazole-κN<sup>3</sup>)
  • Cobinamide, hydroxide sulfite (1:1) (salt), dihydrogen phosphate (ester), inner salt, 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosyl-1H-benzimidazole
  • Cobinamide, sulfite (1:1) (salt), dihydrogen phosphate (ester), 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosylbenzimidazole
  • Cobinamide, sulfite (1:1) (salt), dihydrogen phosphate (ester), inner salt, 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosyl-1H-benzimidazole
  • Cobinamide, sulfite phosphate, 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosylbenzimidazole
  • Sulfiotcobalamine
  • Sulfitocobalamin
  • Vitamin B<sub>12</sub>-sulfonic acid
  • See more synonyms
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Found 4 products.
  • Sulphitocobalamin

    CAS:
    Formula:C62H88CoN13O14P·HO3S
    Molecular weight:1329.38 81.07

    Ref: 4Z-V-035003

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  • Sulfitocobalamin Sodium Salt

    CAS:
    <p>Applications Sulfitocobalamin Sodium Salt is a useful synthetic intermediate in the synthesis of Hydroxocobalamin Acetate (H826800); a physiological analog of vitamin B12 where the CN group is replaced with OH. Exists in aqueous solution as an equilibrium mixture of the hydroxy isomer and the ionic aqua isomer (aquacobalamin). Precursor of the coenzymes methylcobalamin and cobamamide. Coordination Compound. Vitamin (hematopoietic).<br>References Kaczka, E.A., et al.: Science, 112, 354 (1950); Friedrich, W., et al.: Vitamins, 837 (1988); Forsyth, J.C., et al.: Clin. Toxicol., 31, 277 (1993)<br></p>
    Formula:C62H88CoN13NaO17PS
    Color and Shape:Neat
    Molecular weight:1432.4

    Ref: TR-S699360

    10mg
    394.00€
    100mg
    2,640.00€
  • Sulfitocobalamin sodium salt

    CAS:
    <p>Sulfitocobalamin sodium salt is a bacterial strain that is used as a probiotic. It has been shown to be biocompatible and can be used with human liver cells in laboratory studies. Sulfitocobalamin sodium salt is also effective in treating bowel disease, because it reduces the inflammatory response by inhibiting pro-inflammatory cytokine production and preventing the damage of mucosal cells. Sulfitocobalamin sodium salt has been shown to inhibit growth of infectious bacteria, such as Salmonella enterica serovar Typhimurium and Helicobacter pylori, which cause diseases like hepatitis and corrinosis. The molecule also has biological properties that are used for the treatment of inflammation, ulcerative colitis, and other diseases caused by infectious agents.</p>
    Formula:C62H88CoN13NaO17PS
    Purity:Min. 95%
    Molecular weight:1,432.4 g/mol

    Ref: 3D-FS173315

    10mg
    863.00€
    25mg
    1,193.00€
  • Sulphitocobalamin

    CAS:
    Formula:C62H88CoN13O14PHO3S
    Molecular weight:1329.38 : 81.07

    Ref: ST-EA-CP-H13003

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