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Merck

H10401

Hexamethyleneimine

99%

Synonym(s):

1-Azacycloheptane, Azepane, HMI, Perhydroazepine, Hexahydro-1H-azepine, Homopiperidine

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About This Item

Empirical Formula (Hill Notation):
C6H13N
CAS Number:
111-49-9
Molecular Weight:
99.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24895424
EC Number:
203-875-9
Beilstein/REAXYS Number:
1084
MDL number:
MFCD00006934
Assay:
99%
Form:
liquid

Key Documents

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InChI

1S/C6H13N/c1-2-4-6-7-5-3-1/h7H,1-6H2

InChI key

ZSIQJIWKELUFRJ-UHFFFAOYSA-N

SMILES string

C1CCCNCC1

vapor pressure

7.4 mmHg ( 21.1 °C)

assay

99%

form

liquid

refractive index

n20/D 1.466 (lit.)

bp

138 °C/749 mmHg (lit.)

density

0.88 g/mL at 25 °C (lit.)

Quality Level

100

Related Categories

Application

Hexamethyleneimine (HMI) can be used in the preparation of:
  • zeolitic catalysts such as MCM-22 and MCM-49
  • SAPO-35, a molecular sieve
  • various microporous aluminosilicates and titanosilicates
  • organic-inorganic hybrid pervoskite


It can also been used in the total synthesis of various natural products and bioactive molecules such as (−)-balanol, indole estrogens, derivatives of daunorubicin and (+)-cetiedil.

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Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1C - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

64.4 °F - closed cup

flash_point_c

18 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ9491
MKCX8975
MKCX8974
MKCX7840
MKCV3437

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A novel titanosilicate with MWW structure. I. Hydrothermal synthesis, elimination of extra framework titanium, and characterizations.
Wu P, et al.
The Journal of Physical Chemistry B, 105(15), 2897-2905 (2001)
Direct Dual?Template Synthesis of MWW Zeolite Monolayers.
Margarit VJ, et al.
Angewandte Chemie (International Edition in English), 127(46), 13928-13932 (2015)
Formal total synthesis of (-)-balanol: Concise approach to the hexahydroazepine segment based on RCM.
Furstner A and Thiel OR
The Journal of Organic Chemistry, 65(6), 1738-1742 (2000)
J R Lundkvist et al.
Journal of medicinal chemistry, 33(12), 3182-3189 (1990-12-01)
A series of conformationally restricted analogues of the partial muscarinic agonist N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide (BM 5; 1) was synthesized. Three of the racemic derivatives were resolved into the enantiomers. The compounds were investigated for muscarinic and antimuscarinic activity in the isolated guinea
SAPO-35 Molecular Sieve: Synthesis, Characterization, and Adsorbate Interactions of Cu (II) in CuH? SAPO-35.
Prakash AM, et al.
Chemistry of Materials, 10(3), 932-941 (1998)
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