Fatty acid esters
Medchemexpress LLC 3-O-methyldopa (3-methoxy-L-tyrosine) | 300-48-1 | MFCD00037205; MFCD07784093 | 99.9% | 211.21 g/mol | C10H13NO4 | 5 MG
3-O-methyldopa (3-methoxy-L-tyrosine) is an analytical standard and a metabolic derivative of L-DOPA used for research and analytical applications. It can cross the blood-brain barrier and is used in studies of neuropharmacology, Parkinson's disease, and related nervous system disorders. Certificates of analysis are available for batch verification.
- Analytical standard suitable for quantitative analysis.
- Metabolite of L-DOPA that crosses the blood-brain barrier.
- Applicable to neuropharmacology and Parkinson's disease research.
- Supplied as solid and ready-to-use solution formats.
- High purity with batch-specific certificate of analysis available.
ABclonal Technology MonoMethyl-Histone H3-R2 Rabbit pAb
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails, instead, they contain a palindromic termination element. This gene is located separately from the other H3 genes that are in the histone gene cluster on chromosome 6p22-p21.3.
Medchemexpress LLC Dodecanoic acid, ethyl ester | 106-33-2 | HY-W009684 | 99.76% | 228.38 | 5 G
Ethyl Laurate is an organic compound commonly used as a flavoring and food additive. It can be used to make fruit, mint, and sweet flavors, and is widely used in food processing and cosmetic production. Additionally, this compound serves as a reagent and intermediate in certain organic synthesis reactions.
- Used as a flavoring and food additive.
- Can be used to create fruit, mint, and sweet flavors.
- Widely applied in food processing and cosmetic production.
- Functions as a reagent and intermediate in organic synthesis reactions.
- A biochemical reagent for life science-related research.
![Medchemexpress LLC Lauric acid-1-13C | 93639-08-8 | MFCD00002737 | >95.0% | 201.3 | C11[13C]H24O2 | 100mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000268458.png-250.jpg)
Medchemexpress LLC Lauric acid-1-13C | 93639-08-8 | MFCD00002737 | >95.0% | 201.3 | C11[13C]H24O2 | 100mg
Lauric acid-13C is the 13C labeled Lauric acid Lauric acid is a middle chain-free fatty acid with strong bactericidal properties The EC50s for P acnes S aureus S epidermidis are 2 6 4 g/mL respectively
Medchemexpress LLC Lauric acid | 143-07-7 | MFCD00002736 | 99.9% | 200.32 | C12H24O2 | 5g
Lauric acid is a middle chain-free fatty acid with strong bactericidal properties The EC50s for P acnes S aureus S epidermidis are 2 6 4 g/mL respectively[1]
Medchemexpress LLC 9-Hexadecenoic acid, methyl ester, (9Z)- | 1120-25-8 | 98.1% | 268.43 | 250 MG
Methyl palmitoleate, a fatty acid methyl ester, is an analogue of Palmitoleate with cytoprotective and growth-promoting properties. It inhibits the formation and aggregation of wax crystals and improves the low-temperature fluidity of biodiesel as a biodiesel additive.
- Fatty acid methyl ester
- Analogue of Palmitoleate
- Cytoprotective properties
- Growth-promoting properties
- Inhibits the formation and aggregation of wax crystals
- Improves the low-temperature fluidity of biodiesel
eMolecules 29823-18-5 | Ethyl 7-bromoheptanoate | Combi-Blocks | MFCD00037103 | 237.137 | C9H17BrO2 | 98.000 | CCOC(=O)CCCCCCBr | 25g | 232312167
Ethyl 7-bromoheptanoate | Combi-Blocks | 29823-18-5 | MFCD00037103 | 237.137 | C9H17BrO2 | 98.000 | CCOC(=O)CCCCCCBr | 25g | 232312167
Medchemexpress LLC Ethyl hydrogen pimelate | 33018-91-6 | MFCD00014383 | >98.0% | 188.22 g/mol | C9H16O4 | 1 G
Monoethyl pimelate (ethyl hydrogen pimelate) is the monoethyl ester of pimelic acid (C9H16O4; MW 188.22 g/mol). It is supplied as a high-purity research chemical used as a synthetic intermediate and building block in organic synthesis, offering consistent performance for esterification and related transformations.
- High purity (>98%) suitable for synthetic applications.
- Acts as a versatile ester building block for organic synthesis.
- Compatible with common organic solvents and reaction conditions.
- Provides consistent molecular properties (C9H16O4, 188.22 g/mol).
- Safety data sheet and certificate of analysis available.
Medchemexpress LLC Disodium succinate-13C2 | 83587-80-8 | 99.3% | 164.04 g/mol | C4H4Na2O4 | 5 MG
Disodium succinate-13C2 is the 13C2-stable-isotope labeled disodium salt of succinic acid supplied as a small-pack analytical standard for metabolic and biochemical research. It is used as an internal standard or tracer in mass spectrometry, NMR, and isotope-labeling experiments where high isotopic and chemical integrity are required.
- 13C2 stable isotope labeling for tracing and quantification.
- High chemical purity (reported 99.3%) for reliable analytical measurements.
- Small pack size suitable for micro-scale analytical workflows.
- Compatible with mass spectrometry and NMR applications.
- Provides a defined reagent for metabolic flux and isotope tracing studies.
[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C)[C@@H](O)c1ccccc1)OC)N(C)C(=O)[C@@H](NC(=O)[C@@H](NC)C(C)C)C(C)C | 5g | 859973523](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000472916.jpg-250.jpg)
eMolecules 474645-27-7 | Monomethyl auristatin E | Combi-Blocks, Inc. | MFCD22124498 | 717.993 | C39H67N5O7 | 95.000 | CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C)[C@@H](O)c1ccccc1)OC)N(C)C(=O)[C@@H](NC(=O)[C@@H](NC)C(C)C)C(C)C | 5g | 859973523
Monomethyl auristatin E | Combi-Blocks, Inc. | 474645-27-7 | MFCD22124498 | 717.993 | C39H67N5O7 | 95.000 | CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C)[C@@H](O)c1ccccc1)OC)N(C)C(=O)[C@@H](NC(=O)[C@@H](NC)C(C)C)C(C)C | 5g | 859973523