N-Heptafluorobutyrylimidazole - for GC derivatization , CAS No.32477-35-3

CAS: 32477-35-3 Cat. No.: H121494 Molecular Weight: 264.10 Beilstein Registry Number: 4488026 EC Number: 251-063-8
AVAILABLE TO ORDER
GRADE & PURITY for GC derivatization ? GC-derivatization grade — reagents to make analytes GC-amenable (volatile/stable). Use before GC to derivatize polar or thermally labile compounds.
Synonyms
1-(Heptafluorobutyryl)imidazole | 1-(Perfluorobutyryl)imidazole | NSC 151966
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Size
Status
Price
Qty
1g
H121494-1g
2
$19.90
5g
H121494-5g
3
$59.90
25g
H121494-25g
1
$189.90
Enter a quantity for the sizes you want to add.
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Why this grade

for GC derivatization for GC derivatization for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
1-(Heptafluorobutyryl)imidazole | 1-(Perfluorobutyryl)imidazole | NSC 151966
Specifications & Purity
for GC derivatization
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
for GC derivatization
Names and Identifiers
Canonical SmilesC1=CN(C=N1)C(=O)C(C(C(F)(F)F)(F)F)(F)F
IUPAC Name2,2,3,3,4,4,4-heptafluoro-1-imidazol-1-ylbutan-1-one
InChIKeyMSYHGYDAVLDKCE-UHFFFAOYSA-N
INCHI1S/C7H3F7N2O/c8-5(9,6(10,11)7(12,13)14)4(17)16-2-1-15-3-16/h1-3H
Isomeric SMILES C1=CN(C=N1)C(=O)C(C(C(F)(F)F)(F)F)(F)F
WGK Germany 3
Molecular Weight 264.10
Beilstein 4488026
Reaxy-Rn 4488026
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4488026&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassAzoles
SubclassImidazoles
Intermediate Tree Nodes Substituted imidazoles
Direct ParentCarbonylimidazoles
Alternative Parents N-acylimidazoles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organofluorides  Organic oxides  Hydrocarbon derivatives  Alkyl fluorides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents N-acylimidazole - Imidazole-1-carbonyl group - N-substituted imidazole - Heteroaromatic compound - Azacycle - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as carbonylimidazoles. These are substituted imidazoles in which the imidazole ring bears a carbonyl group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

22 results found

Lot NumberCertificate TypeDateItem
B2628566Certificate of AnalysisJan 20, 2026 H121494
B2628591Certificate of AnalysisJan 20, 2026 H121494
B2628431Certificate of AnalysisJan 20, 2026 H121494
L2522060Certificate of AnalysisJul 24, 2025 H121494
H2515304Certificate of AnalysisJul 24, 2025 H121494
H2515303Certificate of AnalysisJul 24, 2025 H121494
H2515302Certificate of AnalysisJul 24, 2025 H121494
F2502121Certificate of AnalysisJul 05, 2024 H121494
F2505089Certificate of AnalysisJul 05, 2024 H121494
G2426426Certificate of AnalysisJul 05, 2024 H121494
G2426429Certificate of AnalysisJul 05, 2024 H121494
L2318277Certificate of AnalysisNov 23, 2023 H121494
L2318278Certificate of AnalysisNov 23, 2023 H121494
L2318279Certificate of AnalysisNov 23, 2023 H121494
G2408070Certificate of AnalysisNov 30, 2022 H121494
D2315335Certificate of AnalysisNov 30, 2022 H121494
C2311112Certificate of AnalysisNov 30, 2022 H121494
J2317016Certificate of AnalysisNov 30, 2022 H121494
C2311097Certificate of AnalysisNov 30, 2022 H121494
F2217279Certificate of AnalysisJun 17, 2022 H121494
F2213242Certificate of AnalysisJun 17, 2022 H121494
J2231123Certificate of AnalysisJun 24, 2021 H121494

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Chemical and Physical Properties
SensitivityMoisture Sensitive;air&light&heat sensitive
Refractive Index1.385
Flash Point(°F)170.6 °F
Flash Point(°C)77°C
Boil Point(°C)160-162°C
Melt Point(°C)10-13°C
Molecular Weight264.100 g/mol
XLogP32.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count9
Rotatable Bond Count2
Exact Mass264.013 Da
Monoisotopic Mass264.013 Da
Topological Polar Surface Area34.900 Ų
Heavy Atom Count17
Formal Charge0
Complexity314.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Zhongfei Zhang, Puyu Yang, Boyan Gao, Guoren Huang, Man Liu, Liangli Lucy Yu.  (2019)  Synthesis of 2-Monochloropanol Fatty Acid Esters and Their Acute Oral Toxicities in Swiss Mice.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:30874433] [10.1021/acs.jafc.9b01083]
2. Yonglin Li, Yancai Li, Yan Guo, Jie Qiang, Yongsheng Cao, Guoyi Qu, Yuan Gao, Qi Li, Xiuzhu Yu.  (2024)  Understanding the formation and mitigation of chloropropanol esters during traditional Chinese cooking using a lipase hydrolysis-based method.  FOOD CHEMISTRY,      [PMID:39647382] [10.1016/j.foodchem.2024.142303]
3. Bing Wang, Fuwei Xie, Mantang Chen, Pingping Shang, Lining Pan, Huapeng Cui, Yaqiong Qin, Li Zhang, Jizhao Guo, Xiaobing Zhang, Cong Nie, Xiaoyu Wang, Shaofeng Liu.  (2025)  A simple derivatization and highly sensitive gas chromatography-mass spectrometry method for the determination of glycidol and 2-/3-monochloropropanediol in heated tobacco product aerosol.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:40865308] [10.1016/j.chroma.2025.466310]
Solution Calculators
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