- Chemical Name: 2-heptadecyl-1H-benzimidazole
- CAS No.: 5805-27-6
Factory Sells Best Quality 2-heptadecyl-1H-benzimidazole 5805-27-6 with USP
- Molecular Formula: C24H40 N2
- Molecular Weight: 356.595
- Vapor Pressure: 4E-10mmHg at 25°C
- Boiling Point: 512.9°Cat760mmHg
- Flash Point: 248.4°C
- PSA： 28.68000
- Density: 0.949g/cm3
- LogP: 7.97680
2-heptadecyl-1H-benzimidazole(Cas 5805-27-6) Usage
|
Family |
Benzimidazole |
|
Physical state |
Solid |
|
Color |
White to off-white |
|
Molecular weight |
359.56 g/mol |
|
Applications |
Corrosion inhibitor, lubricant additive, antimicrobial compound
|
|
Specific content |
HDBI is a synthetic chemical compound
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|
General Description |
2-heptadecyl-1H-benzimidazole, also known as HDBI, is a synthetic chemical compound belonging to the benzimidazole family. It is a white to off-white solid substance with a molecular formula of C24H37N2 and a molecular weight of 359.56 g/mol. HDBI is commonly used as a corrosion inhibitor in industrial applications, particularly for protecting metals such as steel and copper from rust and corrosion. It is also utilized as an additive in lubricants and oils to improve their performance and protect machinery from wear and tear. Additionally, HDBI has shown potential as a biologically active compound with antimicrobial and antifungal properties, making it a promising candidate for various agricultural and pharmaceutical applications. |
InChI:InChI=1/C24H40N2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-24-25-22-19-17-18-20-23(22)26-24/h17-20H,2-16,21H2,1H3,(H,25,26)
5805-27-6 Relevant articles
A silver-induced metal-organic gel based on biscarboxyl-functionalised benzimidazole derivative: Stimuli responsive and dye sorption
Zhang, You-Ming,You, Xing-Mei,Yao, Hong,Guo, Ying,Zhang, Peng,Shi, Bing-Bing,Liu, Jun,Lin, Qi,Wei, Tai-Bao
, p. 39 - 47 (2014)
A multi-responsiveness supramolecular me...
First simple and mild synthesis of 2-alkylbenzimidazoles involving a supported enzymatic catalyst
Renard, Gilbert,Lerner, Dan A.
, p. 1417 - 1420 (2007)
A new enzymatic synthesis is described f...
Trichloroisocyanuric Acid/Triphenylphosphine-Mediated Synthesis of Benzimidazoles, Benzoxazoles, and Benzothiazoles
Rezazadeh, Soodabeh,Akhlaghinia, Batool,Razavi, Nasrin
, p. 145 - 155 (2015/05/05)
A new and efficient method for preparati...
A novel synthetic method for the preparation of aliphatic aldehydes from the corresponding carboxylic acids
Guo, Yuan,Lu, Zhenhuan,Yao, Libo,Shi, Zhen
scheme or table, p. 489 - 492 (2012/01/05)
A novel synthetic method for the prepara...
Enzyme-mediated domino synthesis of 2-alkylbenzimidazoles in solvent-free system: A green route to heterocyclic compound
Wang, Li,Li, Chao,Wang, Na,Li, Kun,Chen, Xi,Yu, Xiao-Qi
body text, p. 16 - 20 (2010/12/19)
Solvent-free domino acylation/cyclizatio...
5805-27-6 Process route
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95-54-5
1,2-diamino-benzene
-
-
57-11-4
stearic acid
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![2-heptadecyl-1H-benzo[d]imidazole](/upload/2026/10/8a4dd47426e8452fbb4979fbd378f316_e211741d-18c7-4a5c-be2d-fe7bacad3eae.png)
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5805-27-6
2-heptadecyl-1H-benzo[d]imidazole
| Conditions | Yield |
|---|---|
|
With
Lypozyme(R);
In
cyclohexane;
at 37 ℃;
for 72h;
|
65%
|
|
|
|
|
at 140 - 150 ℃;
|
|
|
Microwave irradiation;
|
|
|
at 210 ℃;
for 1.5h;
Inert atmosphere;
|
-
-
C36 H50 O2 P(1+) *Cl(1-)
-
-
95-54-5
1,2-diamino-benzene
-
-
5805-27-6
2-heptadecyl-1H-benzo[d]imidazole
| Conditions | Yield |
|---|---|
|
In
1,4-dioxane;
for 2.5h;
Reflux;
|
5805-27-6 Upstream products
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876492-81-8
N?(2?aminophenyl)stearamide
-
95-54-5
1,2-diamino-benzene
-
57-11-4
stearic acid
-
105-28-2
2-heptadecyl-2-imidazoline