1-Methylimidazole - 99%, high purity , CAS No.616-47-7

93 Citations
  • ≥99%
Item Number
M109227
Grouped product items
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M109227-25ml
25ml
In stock
$16.90
M109227-100ml
100ml
In stock
$24.90
M109227-250ml
250ml
In stock
$55.90
M109227-500ml
500ml
In stock
$85.90

Basic Description

Synonyms1-methylimidazole | 1-Methyl-1H-imidazole | 616-47-7 | N-Methylimidazole | 1H-Imidazole, 1-methyl- | IMIDAZOLE, 1-METHYL- | N-methylimidazol | 1-methylimidazol | n-methyl imidazole | DTXSID6052291 | CHEBI:113454 | P4617QS63Y | NSC-88064 | 1-methyl-imidazole | 1-methylimdazole | EINECS
Specifications & Purity≥99%
Storage TempArgon charged
Shipped InNormal
Note25g 售完停产

Associated Targets(Human)

CYP1A2 Tchem Cytochrome P450 1A2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2D6 Tclin Cytochrome P450 2D6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2C19 Tchem Cytochrome P450 2C19 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
DRD1 Tclin D(1A) dopamine receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP3A4 Tclin Cytochrome P450 3A4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2C9 Tchem Cytochrome P450 2C9 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HSD17B10 Tchem 3-hydroxyacyl-CoA dehydrogenase type-2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
FEN1 Tchem Flap endonuclease 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EPHX1 Tchem Epoxide hydrolase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ARSA Tbio Arylsulfatase A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EPHX1 Tchem Epoxide hydrolase 1 (644 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ARSA Tbio Cerebroside-sulfatase (655 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pyogenes (16140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
nfo Endonuclease 4 (425 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

Pubchem Sid488179620
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179620
IUPAC Name 1-methylimidazole
INCHI InChI=1S/C4H6N2/c1-6-3-2-5-4-6/h2-4H,1H3
InChi Key MCTWTZJPVLRJOU-UHFFFAOYSA-N
Canonical SMILES CN1C=CN=C1
Isomeric SMILES CN1C=CN=C1
WGK Germany 1
RTECS NI7000000
PubChem CID 1390
UN Number 2922
Packing Group II
Molecular Weight 82.1
Beilstein 105197
Reaxy-Rn 105197

Certificates

Certificate of Analysis(COA)

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39 results found

Lot NumberCertificate TypeDateItem
I22221019Certificate of AnalysisJun 18, 2024 M109227
I22221020Certificate of AnalysisJun 18, 2024 M109227
F2421345Certificate of AnalysisMar 27, 2024 M109227
F2421344Certificate of AnalysisMar 27, 2024 M109227
F2421376Certificate of AnalysisMar 27, 2024 M109227
E2212048Certificate of AnalysisFeb 22, 2024 M109227
E2212030Certificate of AnalysisFeb 22, 2024 M109227
A2203569Certificate of AnalysisOct 11, 2023 M109227
A2405326Certificate of AnalysisSep 13, 2023 M109227
A2405327Certificate of AnalysisSep 13, 2023 M109227
A2405328Certificate of AnalysisSep 13, 2023 M109227
A2405329Certificate of AnalysisSep 13, 2023 M109227
A2405330Certificate of AnalysisSep 13, 2023 M109227
I2318022Certificate of AnalysisSep 11, 2023 M109227
I2318025Certificate of AnalysisSep 11, 2023 M109227
H2314258Certificate of AnalysisApr 18, 2023 M109227
H2314254Certificate of AnalysisApr 18, 2023 M109227
H2314251Certificate of AnalysisApr 18, 2023 M109227
H2314250Certificate of AnalysisApr 18, 2023 M109227
H2314245Certificate of AnalysisApr 18, 2023 M109227
A2314206Certificate of AnalysisJan 06, 2023 M109227
A2314165Certificate of AnalysisJan 06, 2023 M109227
A2314166Certificate of AnalysisJan 06, 2023 M109227
A2314172Certificate of AnalysisJan 06, 2023 M109227
A2314173Certificate of AnalysisJan 06, 2023 M109227
A2314175Certificate of AnalysisJan 06, 2023 M109227
A2314176Certificate of AnalysisJan 06, 2023 M109227
A2314177Certificate of AnalysisJan 06, 2023 M109227
K2016036Certificate of AnalysisSep 13, 2022 M109227
K2016034Certificate of AnalysisSep 13, 2022 M109227
K2216273Certificate of AnalysisJul 01, 2022 M109227
K2216274Certificate of AnalysisJul 01, 2022 M109227
I22221018Certificate of AnalysisJul 01, 2022 M109227
I22221017Certificate of AnalysisJul 01, 2022 M109227
I22221016Certificate of AnalysisJul 01, 2022 M109227
I22221015Certificate of AnalysisJul 01, 2022 M109227
E2212052Certificate of AnalysisMar 21, 2022 M109227
E2212036Certificate of AnalysisMar 21, 2022 M109227
A2306234Certificate of AnalysisMar 21, 2022 M109227

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Chemical and Physical Properties

SolubilityMiscible with water.
SensitivityHygroscopic & Air sensitive
Refractive Index1.4955-1.4975
Flash Point(°F)197.6 °F
Flash Point(°C)92 °C
Boil Point(°C)198°C
Melt Point(°C)-6°C

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS05
Signal Danger
Hazard Statements

H311:Toxic in contact with skin

H314:Causes severe skin burns and eye damage

H302:Harmful if swallowed

H227:Combustible liquid

Precautionary Statements

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

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 ...

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

P260:Do not breathe dust/fume/gas/mist/vapors/spray.

P270:Do not eat, drink or smoke when using this product.

P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

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

P363:Wash contaminated clothing before reuse.

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

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P317:Get emergency medical help.

P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes.

P316:Get emergency medical help immediately.

WGK Germany 1
RTECS NI7000000
Reaxy-Rn 105197
Class 8 (6.1)

Related Documents

Citations of This Product

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74. Sameer Hussain, Xi Chen, Chaofeng Wang, Yi Hao, Xuemeng Tian, Yulian He, Jing Li, M. Shahid, Parameswar Krishnan Iyer, Ruixia Gao.  (2022)  Aggregation and Binding-Directed FRET Modulation of Conjugated Polymer Materials for Selective and Point-of-Care Monitoring of Serum Albumins.  ANALYTICAL CHEMISTRY,  94  (30): (10685–10694).  [PMID:35849826]
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76. Yunlong Yang, Yuanlong Guo, Jili Yuan, Haibo Xie, Chengtao Gao, Tianxiang Zhao, Qiang Zheng.  (2022)  Agile Construction of Porous Organic Frameworks Pending Carboxylic Acids and Imidazolium-Based Ionic Liquids for the Efficient Fixation of CO2 to Cyclic Carbonates.  ACS Sustainable Chemistry & Engineering,  10  (24): (7990–8001).  [PMID:]
77. Pengqi Wan, Wei Guo, Yuxiu Duan, Mingxiao Deng, Chunsheng Xiao.  (2022)  Photosensitizer-Polypeptide Conjugate with Synergistic Antibacterial Efficacy.  MACROMOLECULAR BIOSCIENCE,  22  (7): (2200105).  [PMID:35526119]
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88. Xu Liao, Baoyou Pei, Ruixun Ma, Lingzheng Kong, Xilin Gao, Jiao He, Xiaoyan Luo, Jinqing Lin.  (2022)  Hypercrosslinked Ionic Polymers with High Ionic Content for Efficient Conversion of Carbon Dioxide into Cyclic Carbonates.  Catalysts,  12  (1): (62).  [PMID:]
89. Haolan Gou, Yingying Zhao, Yanglong Zhou, Wei Wei, Xiaoma Fei, Xiaojie Li, Xiaoya Liu.  (2021)  Effects of different imidazole accelerators on curing behavior and cross-linked network of epoxy resin/phenolic resin/benzoxazine ternary system.  POLYMERS FOR ADVANCED TECHNOLOGIES,  33  (2): (610-626).  [PMID:]
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Solution Calculators