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TacroliMus 8-Propyl Analog (USP)

dihydro-fk 506

CAS: 104987-30-6

Molecular Formula: C44H71NO12

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TacroliMus 8-Propyl Analog (USP) - Names and Identifiers

Name dihydro-fk 506
Synonyms Dihydro-FK506
dihydro-fk 506
TsukubaMycin B
Dihydro-FK506 DIHYDRO-FK506
TacroliMus 8-Propyl Analog (USP)
Tacrolimus EP Impurity E (Dihydro Tacrolimus)
15,19-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone, 5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-[(1E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-propyl-, (3S,4R,5S,8R,9E,12S,14S,...
CAS 104987-30-6
EINECS 806-466-9
InChI InChI=1S/C44H71NO12/c1-10-13-31-19-25(2)18-26(3)20-37(54-8)40-38(55-9)22-28(5)44(52,57-40)41(49)42(50)45-17-12-11-14-32(45)43(51)56-39(29(6)34(47)24-35(31)48)27(4)21-30-15-16-33(46)36(23-30)53-7/h19,21,26,28-34,36-40,46-47,52H,10-18,20,22-24H2,1-9H3/b25-19+,27-21+/t26-,28+,29+,30-,31+,32-,33+,34-,36+,37-,38-,39+,40+,44+/m0/s1

TacroliMus 8-Propyl Analog (USP) - Physico-chemical Properties

Molecular FormulaC44H71NO12
Molar Mass806.03
Density1.18±0.1 g/cm3(Predicted)
Melting Point87-94°C
Boling Point875.5±75.0 °C(Predicted)
Solubility Soluble in DMSO
AppearanceWhite powder
pKa9.97±0.70(Predicted)
Storage Condition2-8℃

TacroliMus 8-Propyl Analog (USP) - Risk and Safety

HS Code2934990002

TacroliMus 8-Propyl Analog (USP) - Introduction

Tacrolimus Impurity 6, also known as Tacrolimus EP Impurity E or Tacrolimus 8-Propylene Analog, is a chemical compound that is closely related to the immunosuppressant drug Tacrolimus (also known as FK506). It is categorized as an impurity, which means it is an unintended product or byproduct that can be found during the manufacturing process of Tacrolimus.

As an analog of Tacrolimus, Tacrolimus Impurity 6 shares a similar chemical structure but may have slightly different properties and effects. It is primarily used for analytical purposes in pharmaceutical research and development. Researchers utilize impurities like Tacrolimus Impurity 6 to identify, analyze, and quantify the impurities present in Tacrolimus formulations.

It is important to note that Tacrolimus Impurity 6 should not be used for human consumption or as a therapeutic agent, as its safety and efficacy have not been established for such purposes. Instead, its significance lies in its role as a reference standard, helping researchers ensure the quality, purity, and potency of Tacrolimus drugs on the market.

In summary, Tacrolimus Impurity 6 (Tacrolimus EP Impurity E or Tacrolimus 8-Propylene Analog) is an impurity commonly detected in Tacrolimus formulations. It serves as a reference standard for research purposes, allowing scientists to study and monitor impurities in order to ensure the quality of Tacrolimus medications.

Last Update:2024-04-09 19:05:42
TacroliMus 8-Propyl Analog (USP)
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View History
TacroliMus 8-Propyl Analog (USP)
4-(((2-氯嘧啶-5-基)氧基)甲基)哌啶-1-羧酸叔丁酯
N-[2-[(4-AMINO-3-METHYLPHENYL)ETHYLAMINO]ETHYL]METHANESULFONAMIDE SESQUISULFATE MONOHYDRATE
苄基二(2-羟乙基)甲基氢氧化铵
1-叔丁基二甲硅基咪唑[叔丁基二甲基硅化剂]
2-(3-硝基苯亚甲基)-3-氧代丁酸(2-甲氧基乙基)酯
Benzaldehyde, 4-[(2-methoxyethoxy)methoxy]-
(ALPHAS)-ALPHA-氨基环己烷丁酸
CUPRIC CHLORIDE DIHYDRATE ACS REAGENT
4-氰基吡啶 N-氧化物(托匹司他中间体)
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