1-Hexyne - 97%, high purity , CAS No.693-02-7

  • ≥97%
Item Number
H106703
Grouped product items
SKUSizeAvailabilityPrice Qty
H106703-5ml
5ml
5
$11.90
H106703-10ml
10ml
2
$17.90
H106703-25ml
25ml
7
$34.90
H106703-100ml
100ml
4
$123.90

Basic Description

SynonymsEINECS 211-736-9 | H0140 | FT-0607892 | F0001-1799 | 1-Hexyne, 97% | AMY1242 | Q161638 | Hex-1-yne | CH3(CH2)3C#CH | NSC9709 | NSC-9709 | n-hexyne | UNII-5FZF2F38F5 | 5FZF2F38F5 | HEXYNE | CHEBI:176793 | MFCD00009504 | 1-hexyn | Butylacetylene | DTXSID308
Specifications & Purity≥97%
Storage TempArgon charged
Shipped InNormal
Product Description

1-Hexyne reacted with thianthrene cation radical tetrafluoroborate to form trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborate
Usually used in the synthesis of a tricyclic isoindolinone scaffold by undergoing hydrozirconation and ring-closing metathesis (RCM).

AI Insight

Names and Identifiers

Pubchem Sid488181720
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181720
IUPAC Name hex-1-yne
INCHI InChI=1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3
InChi Key CGHIBGNXEGJPQZ-UHFFFAOYSA-N
Canonical SMILES CCCCC#C
Isomeric SMILES CCCCC#C
WGK Germany 3
RTECS MQ9691000
PubChem CID 12732
UN Number 3295
Molecular Weight 82.14
Beilstein 635687
Reaxy-Rn 635687

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.

12 results found

Lot NumberCertificate TypeDateItem
K1905124Certificate of AnalysisMar 04, 2025 H106703
D2314052Certificate of AnalysisJan 07, 2025 H106703
D2501422Certificate of AnalysisJul 11, 2024 H106703
D2501429Certificate of AnalysisJul 11, 2024 H106703
H2206202Certificate of AnalysisMay 07, 2024 H106703
H2206205Certificate of AnalysisMay 07, 2024 H106703
H2206206Certificate of AnalysisMay 07, 2024 H106703
H2131252Certificate of AnalysisJun 06, 2023 H106703
H2131253Certificate of AnalysisJun 06, 2023 H106703
H2131254Certificate of AnalysisJun 06, 2023 H106703
H2131256Certificate of AnalysisJun 06, 2023 H106703
D2318192Certificate of AnalysisJul 23, 2022 H106703

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Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS07,   GHS02
Signal Danger
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H225:Highly Flammable liquid and vapor

H304:May be fatal if swallowed and enters airways

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P370+P378:In case of fire: Use ... to extinguish.

P210:Keep away from heat, hot surface, sparks, open flames and other ignition sources. - No smoking.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P233:Keep container tightly closed.

P240:Ground/bond container and receiving equipment.

P264:Wash hands [and …] thoroughly after handling.

P403+P235:Store in a well-ventilated place. Keep cool.

P303+P361+P353:IF ON SKIN (or hair): Take off Immediately all contaminated clothing. Rinse SKIN with water [or shower].

P271:Use only outdoors or in a well-ventilated area.

P241:Use explosion-proof [electrical/ventilating/lighting/.../] equipment.

P331:Do NOT induce vomiting.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P242:Use only non-sparking tools.

P243:Take precautionary measures against static discharge.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS MQ9691000
Reaxy-Rn 635687

Related Documents

Reviews

Customer Reviews

Citations of This Product

1. Yanan Liu, Jiaying Zhao, Junting Feng, Yufei He, Yiyun Du, Dianqing Li.  (2018)  Layered double hydroxide-derived Ni-Cu nanoalloy catalysts for semi-hydrogenation of alkynes: Improvement of selectivity and anti-coking ability via alloying of Ni and Cu.  JOURNAL OF CATALYSIS,  359  (251).  [PMID:] [10.1016/j.jcat.2018.01.009]
2. Yujing Zuo, Dengxu Wang, Jie Zhang, Shengyu Feng.  (2014)  Multifunctional alkoxysilanes prepared by thiol–yne “click” chemistry: their luminescence properties and modification on a silicon surface.  RSC Advances,  (108): (62827-62834).  [PMID:] [10.1039/C4RA13620A]

References

1. Zhiguo Li,Champika N Weeraman,Julianne M Gibbs-Davis.  (2014-05-08)  Following the azide-alkyne cycloaddition at the silica/solvent interface with sum frequency generation..  Chemphyschem : a European journal of chemical physics and physical chemistry,  15  ((11)): (2247-2251).  [PMID:24800780]
2. Emma Oakton,Gianvito Vilé,Daniel S Levine,Eva Zocher,David Baudouin,Javier Pérez-Ramírez,Christophe Copéret.  (2014-09-03)  Silver nanoparticles supported on passivated silica: preparation and catalytic performance in alkyne semi-hydrogenation..  Dalton transactions (Cambridge, England : 2003),  43  ((40)): (15138-15142).  [PMID:25178410]
3. He Nan,Cheng Zhang,Amrit Venkatesh,Aaron J Rossini,Jared L Anderson.  (2017-06-26)  Argentation gas chromatography revisited: Separation of light olefin/paraffin mixtures using silver-based ionic liquid stationary phases..  Journal of chromatography. A,  1523  (316-320).  [PMID:28647149]
4. Davide Albani,Masoud Shahrokhi,Zupeng Chen,Sharon Mitchell,Roland Hauert,Núria López,Javier Pérez-Ramírez.  (2018-07-08)  Selective ensembles in supported palladium sulfide nanoparticles for alkyne semi-hydrogenation..  Nature communications,  ((1)): (2634-2634).  [PMID:29980682]
5. Hyomin Jin,Seonah Kim,Hye Jin Bae,Ji Hye Lee,Hyonseok Hwang,Myung Hwan Park,Kang Mun Lee.  (2019-01-10)  Effect of Planarity of Aromatic Rings Appended to o-Carborane on Photophysical Properties: A Series of o-Carboranyl Compounds Based on 2-Phenylpyridine- and 2-(Benzo[b]thiophen-2-yl)pyridine..  Molecules (Basel, Switzerland),  24  ((1)):   [PMID:30621119]
6. Bettina Miller,Shuli Mao,Kara M George Rosenker,Joshua G Pierce,Peter Wipf.  (2012-09-29)  Synthesis of a library of tricyclic azepinoisoindolinones..  Beilstein journal of organic chemistry,  (1091-1097).  [PMID:23019435]
7. Mauricio M Victor,Ravir R Farias,Danielle L da Silva,Paulo H F do Carmo,Maria A de Resende-Stoianoff,Cláudio Viegas,Patrícia F Espuri,Marcos J Marques.  (2018-10-27)  Synthesis and Evaluation of Antifungal and Antitrypanosomastid Activities of Symmetrical 1,4-Disubstituted-1,2,3-Bistriazoles Obtained by CuAAC Conditions..  Medicinal chemistry (Shariqah (United Arab Emirates)),  15  ((4)): (400-408).  [PMID:30360747]
8. Yanan Liu, Jiaying Zhao, Junting Feng, Yufei He, Yiyun Du, Dianqing Li.  (2018)  Layered double hydroxide-derived Ni-Cu nanoalloy catalysts for semi-hydrogenation of alkynes: Improvement of selectivity and anti-coking ability via alloying of Ni and Cu.  JOURNAL OF CATALYSIS,  359  (251).  [PMID:] [10.1016/j.jcat.2018.01.009]
9. Yujing Zuo, Dengxu Wang, Jie Zhang, Shengyu Feng.  (2014)  Multifunctional alkoxysilanes prepared by thiol–yne “click” chemistry: their luminescence properties and modification on a silicon surface.  RSC Advances,  (108): (62827-62834).  [PMID:] [10.1039/C4RA13620A]

Solution Calculators