244422
1-Hexyne
97%
Synonym(s):
Butylacetylene, n-Butylacetylene
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About This Item
Linear Formula:
CH3(CH2)3C≡CH
CAS Number:
Molecular Weight:
82.14
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39010407
UNSPSC Code:
12352100
EC Number:
211-736-9
MDL number:
Beilstein/REAXYS Number:
635687
Assay:
97%
Form:
liquid
vapor pressure
253 mmHg ( 37.7 °C)
Quality Level
assay
97%
form
liquid
impurities
<2% 1-bromobutane
refractive index
n20/D 1.399 (lit.)
bp
71-72 °C (lit.)
mp
−132 °C (lit.)
density
0.715 g/mL at 25 °C (lit.)
SMILES string
CCCCC#C
InChI
1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3
InChI key
CGHIBGNXEGJPQZ-UHFFFAOYSA-N
General description
1-Hexyne reacted with thianthrene cation radical tetrafluoroborate to form trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborate.
Application
1-Hexyne was used in the synthesis of a tricyclic isoindolinone scaffold by undergoing hydrozirconation and ring-closing metathesis (RCM).
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signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-4.0 °F - closed cup
flash_point_c
-20 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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David A Bichara et al.
The Journal of arthroplasty, 33(8), 2666-2670 (2018-05-23)
Wear resistance of ultrahigh molecular weight polyethylene (UHMWPE) is improved via ionizing radiation crosslinking and subsequent high temperature melting for improved toughness. Our group has previously reported that crosslinking can also be achieved chemically using organic peroxides. However, volatile peroxide
Bettina Miller et al.
Beilstein journal of organic chemistry, 8, 1091-1097 (2012-09-29)
Hydrozirconation of 1-hexyne, the addition to in situ prepared N-acyliminium species, and ring-closing metathesis (RCM) were key steps in the preparation of a tricyclic isoindolinone scaffold. An unusual alkene isomerization process during the RCM was identified and studied in some
Mauricio M Victor et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 15(4), 400-408 (2018-10-27)
The trypanosomatids, such as the protozoan Leishmania spp., have a demand by ergosterol, which is not present in the membrane from mammal cells. The suppression of the synthesis of ergosterol would be a new target of compounds with leishmanicidal activity
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 244422-100ML | 04061825759920 |
| 244422-25ML | 04061825759937 |