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N-(2-Hydroxyethyl)hexamethyleneimine - 95%, high purity , CAS No.20603-00-3

    Grade & Purity:
  • ≥95%
In stock
Item Number
H168438
Grouped product items
SKU Size
Availability
Price Qty
H168438-250mg
250mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9.90
H168438-1g
1g
2
$15.90
H168438-5g
5g
3
$28.90
H168438-25g
25g
4
$95.90
H168438-100g
100g
2
$345.90
H168438-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,554.90

Basic Description

Synonyms EINECS 243-915-2 | SCHEMBL227313 | 2-(1-Azepanyl)ethanol | 1H-Azepine-1-ethanol, hexahydro- | 2-(azepan-1-yl)ethanol | WAY-358400-A | TS-01874 | NSC 50608 | J-013456 | DTXSID00174619 | 2-azaperhydroepinylethan-1-ol | FT-0608810 | 1-(4-methylphenyl)thioure
Specifications & Purity ≥95%
Storage Temp Argon charged
Shipped In Normal
Product Description

Application

N-(2-Hydroxyethyl)hexamethyleneimine is used in organic synthesis, building blocks. It is mainly involved as an intermediate in the synthesis of Bazedoxifene acetate.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Azepanes
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Azepanes
Alternative Parents Trialkylamines  1,2-aminoalcohols  Azacyclic compounds  Primary alcohols  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Azepane - 1,2-aminoalcohol - Tertiary amine - Tertiary aliphatic amine - Alkanolamine - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Amine - Organic oxygen compound - Alcohol - Aliphatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as azepanes. These are organic compounds containing a saturated seven member heterocycle, with one nitrogen atom.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 488186508
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488186508
IUPAC Name 2-(azepan-1-yl)ethanol
INCHI InChI=1S/C8H17NO/c10-8-7-9-5-3-1-2-4-6-9/h10H,1-8H2
InChIKey VMRYMOMQCYSPHS-UHFFFAOYSA-N
Smiles C1CCCN(CC1)CCO
Isomeric SMILES C1CCCN(CC1)CCO
Molecular Weight 143.231
Reaxy-Rn 104110
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104110&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

21 results found

Lot Number Certificate Type Date Item
A2220409 Certificate of Analysis Apr 03, 2025 H168438
A2220368 Certificate of Analysis Nov 07, 2024 H168438
J2418727 Certificate of Analysis Jun 18, 2024 H168438
J2422495 Certificate of Analysis Jun 18, 2024 H168438
K2419449 Certificate of Analysis Jun 18, 2024 H168438
I2115212 Certificate of Analysis Jun 17, 2024 H168438
H2126312 Certificate of Analysis Jun 17, 2024 H168438
F2001112 Certificate of Analysis Mar 14, 2023 H168438
A2309135 Certificate of Analysis Nov 03, 2022 H168438
A2309136 Certificate of Analysis Nov 03, 2022 H168438
A2306602 Certificate of Analysis Nov 03, 2022 H168438
A2306603 Certificate of Analysis Nov 03, 2022 H168438
A2306463 Certificate of Analysis Nov 03, 2022 H168438
A2306445 Certificate of Analysis Nov 03, 2022 H168438
A2306466 Certificate of Analysis Nov 03, 2022 H168438
A2306450 Certificate of Analysis Nov 03, 2022 H168438
A2306451 Certificate of Analysis Nov 03, 2022 H168438
B2427253 Certificate of Analysis Dec 11, 2021 H168438
A2429365 Certificate of Analysis Dec 11, 2021 H168438
A2220419 Certificate of Analysis Dec 11, 2021 H168438
I2221023 Certificate of Analysis Dec 11, 2021 H168438

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Chemical and Physical Properties

Solubility Fully miscible in water.
Sensitivity air sensitive
Boil Point(°C) 114-115°/23mm
Molecular Weight 143.230 g/mol
XLogP3 1.300
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 2
Exact Mass 143.131 Da
Monoisotopic Mass 143.131 Da
Topological Polar Surface Area 23.500 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 77.300
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Jiapeng Deng, Su Liu, Guoqing Li, Yien Zheng, Weifei Zhang, Jianjing Lin, Fei Yu, Jian Weng, Peng Liu, Hui Zeng.  (2023)  pH-sensitive charge-conversion cinnamaldehyde polymeric prodrug micelles for effective targeted chemotherapy of osteosarcoma in vitro.  Frontiers in Chemistry,  11  (1190596). 
2. Zhiqiang Lin, Junfeng Ding, Xuesi Chen, Chaoliang He.  (2023)  pH- and Temperature-responsive Hydrogels Based on Tertiary Amine-modified Polypeptides for Stimuli-responsive Drug Delivery.  Chemistry-An Asian Journal,  18  (8): (e202300021). 
3. Qianqian Qi, Xianwu Zeng, Licong Peng, Hailiang Zhang, Miao Zhou, Jingping Fu, Jianchao Yuan.  (2020)  Tumor-targeting and imaging micelles for pH-triggered anticancer drug release and combined photodynamic therapy.  JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION,     
4. Ming Zhao, Chunting He, Xueyun Zheng, Min Jiang, Zhiqiang Xie, Hongjiao Wei, Shujun Zhang, Ying Lin, Jiaheng Zhang, Xun Sun.  (2024)  Self-adjuvanting polymeric nanovaccines enhance IFN production and cytotoxic T cell response.  JOURNAL OF CONTROLLED RELEASE,  369  (556). 

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