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Trityl candesartan

CAS No.
139481-72-4
Chemical Name:
Trityl candesartan
Synonyms
Triphenyl Candesartan;TRITYL CANDESARTAN;N-tityl candesartan;Trityl Candesaratan;N-Trityl Candesartan;N-trimethylcandesartan;Trityl Candesartan (C9);Tricycliccandesartan(C9);Candesartan Impurity 8;CANDESARTAN INTERMEDIATE A
CBNumber:
CB0763835
Molecular Formula:
C43H34N6O3
Molecular Weight:
682.77
MDL Number:
MFCD08436154
MOL File:
139481-72-4.mol
MSDS File:
SDS
Last updated:2026-07-16 07:06:08

Trityl candesartan Properties

Melting point 163-165°C
Boiling point 908.6±75.0 °C(Predicted)
Density 1.26±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly, Heated)
form Solid
pka 2.06±0.10(Predicted)
color White to Off-White

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H410
Precautionary statements  P264-P270-P301+P312-P330-P501-P273-P391-P501
REACH Registrations Active

Trityl candesartan price More Price(41)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological 022551 N-Trityl Candesartan 139481-72-4 10mg $453 2026-06-03 Buy
Biosynth FT28595 N-Trityl candesartan 139481-72-4 5g $354 2026-06-04 Buy
Biosynth FT28595 N-Trityl candesartan 139481-72-4 10g $531 2026-06-04 Buy
Biosynth FT28595 N-Trityl candesartan 139481-72-4 25g $885 2026-06-04 Buy
ChemScene CS-W006659 Trityl candesartan ≥98% 139481-72-4 5g $240 2026-06-04 Buy
Product number Packaging Price Buy
022551 10mg $453 Buy
FT28595 5g $354 Buy
FT28595 10g $531 Buy
FT28595 25g $885 Buy
CS-W006659 5g $240 Buy

Trityl candesartan Chemical Properties,Uses,Production

Chemical Properties

Off-White Solid

Uses

2-Ethoxy-1-((2''-(1-trityl-1H-tetrazol-5-yl)-[1,1''-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole-7-carboxylic Acid can be used as reagent/reactant in preparation of the anti-hypertensive drug candesartan cilexetil.

Uses

Candesartan analog as angiotensin II antagonist.

Synthesis

Triphenylmethyl Chloride

76-83-5

Candesartan

139481-59-7

Trityl candesartan

139481-72-4

I. 1-((2'-(2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylic acid (10 kg) was added to the reaction kettle along with dichloromethane (100 kg), and cooled down to 15°C. The temperature of the reaction system was increased to 15°C by adding triethylamine (4.5 kg). Triethylamine (4.5 kg) was slowly added dropwise, and after the dropwise addition was completed, the temperature of the reaction system was raised to 23 °C. Triphenylchloromethane (7kg) was added in batches and after completion of addition, the reaction was maintained at 23°C for 3.5 hours. The reaction progress was monitored by TLC (unfolding agent: dichloromethane/methanol=10:1, v/v, Rf=0.78). After completion of the reaction, the pH of the system was adjusted to 5.4 by adding 0.1 mol/L HCl (30 L), then 5 L of 9 mol/L HCl was added slowly to pH=2.2, and the reaction was allowed to stand for stratification to separate the aqueous and organic layers. The organic layer (about 60 L) was washed with saturated saline, transferred to a reduced pressure distillation unit, and dichloromethane was recovered under reduced pressure. Ethanol (65L) was added to the residue, warmed to 45°C and stirred for 3 hours until a large amount of white solid precipitated. The heating was stopped, cooled to room temperature, filtered, the filter cake was washed with a small amount of ethanol, and dried at 50°C under normal pressure for 12 hours to obtain 2-ethoxy-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole-7-carboxylic acid (white crystalline powder, 14.5 kg, yield 94.0%).

References

[1] Patent: CN105153124, 2018, B. Location in patent: Paragraph 0005; 0054; 0055; 0076; 0090
[2] Patent: WO2009/7986, 2009, A1. Location in patent: Page/Page column 13
[3] Patent: US2010/210852, 2010, A1. Location in patent: Page/Page column 5
[4] Patent: WO2009/7986, 2009, A1. Location in patent: Page/Page column 14

Trityl candesartan Preparation Products And Raw materials

Global( 242)Suppliers
Supplier Tel Email Country ProdList Advantage
Adamas Reagent, Ltd. 400-6009262 15618770481 yhx@titansci.com China 14098 59
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15350 60
XiaoGan ShenYuan ChemPharm co,ltd 15527621225; 15527621225 1791901229@qq.com China 6746 52
BioBioPha Co., Ltd. 0871-65217109 y.liu@mail.biobiopha.com China 5641 65
S.Z. PhyStandard Bio-Tech. Co., Ltd. 0755-83725681-603 China 4484 50
Moltt Biocem Co., Ltd. +86-21-38682181 15900741819 China 281 55
Shanghai Huikai Chemical Technology Co., Ltd. 021-61995394 18916691159 chemicalsea@163.com China 1970 58
HBCChem, Inc. +1-510-219-6317 sales@hbcchem.com United States 10628 60
Quality Control Solutions Ltd. 0755-66853366 13670046396 orders@qcsrm.com China 18188 56
Wuxi Zhongkun Biochemical Technology Co., Ltd. 0510-85629785 18013409632; sales@reading-chemicals.com China 15165 58

View Lastest Price from Trityl candesartan manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Trityl candesartan pictures 2026-07-16 Trityl candesartan
139481-72-4
1kg 98% 1000kgs Shaanxi Dideu New Materials Co. Ltd
Trityl Candesartan pictures 2025-04-15 Trityl Candesartan
139481-72-4
$120.00 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
Trityl candesartan pictures 2022-09-29 Trityl candesartan
139481-72-4
$28.00-30.00 1Kg 99.0% up 50 tons per month Xinxiang Hongqi District Houyuan Trading Co.,Ltd
  • Trityl candesartan pictures
  • Trityl candesartan
    139481-72-4
  • $28.00-30.00
  • 99.0% up
  • Xinxiang Hongqi District Houyuan Trading Co.,Ltd
Candesartan N1-Trityl IMpurity 2-Ethoxy-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole-7-c 2-Ethoxy-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole- 2-ethoxy-1-[[(2'-(1-triphenylmethyl-1h-tetrazol-5-yl)biphenyl-4-yl)methyl]benzimidazole-7-carboxylic acid TRITYL CANDESARTAN (Trityl candesartan)2-Ethoxy-1-[[2-(2-Triphenyl Methyl)-2H-Tetrazole-5-YL](1,1-Biphenyl)-4-YL]Methyl]Benzimidazole-2-Carboxylic Acid 1H-Benzimidazole-7-carboxylic acid, 2-ethoxy-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]- 2-Ethoxy-1-[[(2’-(1-triphenylmethyl-1H-tetrazol-5-yl)biphenyl-4-yl-)methyl]benzimidazole-7-carboxylicacid Triphenyl Candesartan TRITYL CANDESARTAN ( FOR CANDESARTAN CILEXETIL ) TritylCandesartan[CandesartabCilexetilIntermediates] TritylCandesartan,CandesartanCilexetil (1H)-Benzimidazole-7-carboxylicacid CANDESARTAN INTERMEDIATE A 2-ethoxy-3-[[4-[2-[1-(triphenylmethyl)-5-tetrazolyl]phenyl]phenyl]methyl]-4-benzimidazolecarboxylic acid Candesartan Cilexetil Impurity 9 2-Ethoxy-1-[[2-(2-Triphenylmethyl)-2H-Tetrazole-5-Yl](1,1-Biphenyl)-4-Yl]-Methyl]Benzimidazole-7-Carboylicacid 2-ethoxy-1-[[(2-(1-triphenylmethyl-1Htetrazol-5-yl)biphenyl-4-yl-) N-Trityl Candesartan Trityl candesartan/2-Ethoxy-1-[[(2'-(1-triphenylmethyl-1H-tetrazol-5-yl)biphenyl-4-yl)methyl]benzimidazole-7-carboxylic acid 2-ETHOXY-1-[[(2-(1-TRIPHENYLMETHYL-1H-TETRAZOL-5-YL)BIPHENYL)METHYL] BENZIMIDAZOLE-7-CARBOXYLIC ACID Candesartan Impurity 8 1H-benzimidazole-7-carboxylic acid, 1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-2-ethoxy Candesartan Cilexetil Impurity 14 Trityl Candesartan (C9) N-trimethylcandesartan Trityl candesartan USP/EP/BP 2-Ethoxy-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole-7-carboxylic Acid DISCONTINUED 2-Ethoxy-1-[[2?-[2-(Triphenylmethyl)-2H-Tetrazol-5- Yl][1,1?-Biphenyl]-4-Yl]Methyl]-1H-Benzimidazole-7- Carboxylic Acid [N-Trityl Candesartan] Candesartan Cilexetil Intermediate 5 N-tityl candesartan 2-Ethoxy-1-[[2'-(N-triphenylmethyltetrazol-5-yl)-biphenyl-4-yl]methyl]benzimidazole-7-carboxylic acid Trityl Candesaratan 2-Ethoxy-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-benzo[d]imidazole-7-carboxylic acid Triphenyl candesartan ester Trityl candesartan (Candesartan Cilexetil Impurity) Tricycliccandesartan(C9) 139481-72-4 C43H34N6O3 Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Intermediates of Candesartan Candesartan Cilexetil API intermediates INTERMEDIATESOF Intermediates