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D22401

Sigma-Aldrich

1,8-Diaminooctane

98%

Synonym(s):

1,8-Octanediamine, Octamethylenediamine

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About This Item

Linear Formula:
NH2(CH2)8NH2
CAS Number:
373-44-4
Molecular Weight:
144.26
Beilstein:
1735426
EC Number:
206-764-3
MDL number:
MFCD00008248
UNSPSC Code:
12352100
PubChem Substance ID:
24893667
NACRES:
NA.22
form:
crystals
Assay:
98%
Pricing and availability is not currently available.

Quality Level

100

Assay

98%

form

crystals

bp

225-226 °C (lit.)

mp

50-52 °C (lit.)

SMILES string

NCCCCCCCCN

InChI

1S/C8H20N2/c9-7-5-3-1-2-4-6-8-10/h1-10H2

InChI key

PWGJDPKCLMLPJW-UHFFFAOYSA-N

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Application

1,8-Diaminooctane is generally used as crosslinker or spacer during the synthesis of variety of molecular cages, macrocycles and microporous materials.[1][2][3][4][5]

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314,H317

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

222.8 °F - DIN 51758

Flash Point(C)

106 °C - DIN 51758

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL3740
STBL2042
STBK9424
STBK9961
STBK0863

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Jong-Hun Noh et al.
Current microbiology, 74(12), 1417-1424 (2017-08-22)
The isolated Chryseobacterium ginsengiterrae sp. nov DCY68
Template synthesis of Co (II) complexes of tetraazamacrocycles.
Rai PK, et al.
Zeitschrift fur Naturforschung, B: Chemical Sciences, 47(12), 1701-1706 (1992)
Solvent-free covalent functionalization of multi-walled carbon nanotubes and nanodiamond with diamines: looking for cross-linking effects.
Basiuk EV, et al
Applied Surface Science, 259, 465-476 (2012)
Inclusion of a small molecule in a big cage: preparation and structure of catena-[catena-(.alpha.,.omega.-diaminooctane) cadmium-.mu.-tetracyanonickelate]-toluene (1/1).
Hasegawa T, et al.
Inorganic Chemistry, 30(7), 1441-1444 (1991)
Synthesis of New Aza Macrocyclic Diamides 2, 2??Diaminodiphenyl Sulfide Using Crab?Like Method.
Shockravi A and Kamali M
Journal of Heterocyclic Chemistry, 49(3), 499-503 (2012)
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