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Tris(2-aminoethanol) chromium(III) complex trihydrate, also known as chromium(III) tris(2-aminoethanol) trihydrate or Cr(III)-TAC, is a coordination complex of chromium with the chemical formula [Cr(C2H8NO)3]·3H2O. It consists of a central chromium(III) ion coordinated to three 2-aminoethanol ligands, with each ligand donating two oxygen atoms from its hydroxyl groups and one nitrogen atom from its amine group. The complex also contains three water molecules of crystallization. tris(2-aminoethanol) chromium(III) complex trihydrate is used as a dietary supplement to support insulin function and glucose metabolism, particularly for individuals with diabetes or chromium deficiency. It is known for its potential role in improving blood sugar control and may have applications in weight management and athletic performance. However, it is important to note that the safety and efficacy of chromium supplements, including this complex, are subjects of ongoing research and debate.

38819-71-5

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38819-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38819-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,1 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38819-71:
(7*3)+(6*8)+(5*8)+(4*1)+(3*9)+(2*7)+(1*1)=155
155 % 10 = 5
So 38819-71-5 is a valid CAS Registry Number.

38819-71-5Downstream Products

38819-71-5Relevant academic research and scientific papers

Protonation and aquation of chromium(III)/ethanolamine complexes in aqueous solution

Kolosci, Lois,Schug, Kenneth

, p. 3053 - 3056 (2008/10/08)

Several Cr(III) complexes with amino alcohols have been prepared, and the solution chemistry of the tris(2-aminoethanol) complex has been studied in detail. Addition of excess strong acid to solutions containing Cr(Eta)30 (Eta = bidentate aminoalkoxy) results in the following sequence of reactions: stage I, instantaneous protonation to produce bidentate Cr(EtaH)33+ (EtaH = 2-aminoethanol); stage II, rapid (complete in ~10 min at 20°C) conversion to monodentate Cr(EtaH)3(OH2)33+ by ring opening at the alcohol function; stage III, slower stepwise aquation of the N-bonded ethanolamine to produce Cr(OH2)63+. The first-order rate constants in stage III (25°C, μ = 0.10) are k3→2 = 2.3 × 10-4 s-1, k2→1 = 1.7 × 10-5 s-1, and k1→0 = 6.4 × 10-7 s-1. Aquation rates in stages II and III (k1→0) are much faster than normal for Cr(III) complexes but have a precedent in the Cr(III)/ethylene glycol system.

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