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L-2-Aminobutyric Acid-[d6] is a labelled L-2-Aminobutyric Acid. L-2-Aminobutyric Acid is a non-proteogenic amino acid in the class of L-alpha-amino acids, which are commonly found in human kidney and liver tissues. Synonyms: L-2-Aminobutyric-2,3,3,4,4,4-d6 Acid; L-α-Aminobutyric Acid-d6; (S)-2-Aminobutanoic Acid-d6; H-L-Abu-OH-d6; (+)-2-Aminobutanoic Acid-d6; (+)-2-Aminobutyric Acid-d6; (+)-α-Aminobutyric Acid-d6; (2S)-2-Aminobutanoic Acid-d6; (S)-(+)-α-Aminobutyric Acid-d6; (S)-2-Aminobutyric Acid-d6; L-2-Amino-n-butyric Acid-d6; L-2-Aminobutanoic Acid-d6; L-2-Aminobutyric Acid-d6; L-Butyrine-d6; L-Ethylglycine-d6; L-Homoalanine-d6; L-α-Amino-n-butyric Acid-d6; NSC 97060-d6; S-Butyrine-d6. Grade: 95% by HPLC; 98% atom D. CAS No. 1276197-51-3. Molecular formula: C4H3D6NO2. Mole weight: 109.16.
L-2-Aminohexanoic acid amide (L-Norleucine amide) hydrochloride is a kind of biological materials or organic compounds that are widely used in life science research. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Norleucine amide hydrochloride; H-Nle-NH2 hydrochloride. CAS No. 94787-97-0. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-W099801.
L-2-Aminomethylphenylalanine
L-2-Aminomethylphenylalanine. Synonyms: L-Phe(2-CH2NH2)-OH. Grade: ≥ 99% by HPLC. CAS No. 158149-99-6. Molecular formula: C10H14N2O2. Mole weight: 194.23.
L-2-Amino methyl phenylalanine
L-2-Amino methyl phenylalanine. Group: Biochemicals. Grades: Reagent Grade. CAS No. 158149-99-6. Pack Sizes: 1g, 5g. US Biological Life Sciences.
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L-2-Carbamoylphenylalanine
L-2-Carbamoyl phenyl alanine. Group: Biochemicals. Alternative Names: (2S) -2-Amino-3- (2-carbamoylphenyl) propanoic acid. Grades: Highly Purified. Pack Sizes: 250mg, 500mg, 1g, 2g. US Biological Life Sciences.
Worldwide
L-2-Carbamoylphenylalanine 98+% (TLC)
L-2-Carbamoylphenylalanine 98+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 2.5g. US Biological Life Sciences.
L-2-Hydroxybutyric acid (CAS# 3347-90-8) is used in method for preparing Cationic Electrodeposition coating compounds. Synonyms: S-2-hydroxybutyric acid. CAS No. 3347-90-8. Molecular formula: C4H8O3. Mole weight: 104.1.
L-2-hydroxycarboxylate dehydrogenase (NAD+)
The enzyme from the archaeon Methanocaldococcus jannaschii acts on multiple (S)-2-hydroxycarboxylates including (2R)-3-sulfolactate, (S)-malate, (S)-lactate, and (S)-2-hydroxyglutarate. Note that (2R)-3-sulfolactate has the same stereo configuration as (2S)-2-hydroxycarboxylates. Group: Enzymes. Synonyms: (R)-sulfolactate:NAD+ oxidoreductase; L-sulfolactate dehydrogenase; (R)-sulfolactate dehydrogenase; L-2-hydroxyacid dehydrogenase (NAD+); ComC. Enzyme Commission Number: EC 1.1.1.337. CAS No. 81210-65-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0251; L-2-hydroxycarboxylate dehydrogenase (NAD+); EC 1.1.1.337; 81210-65-3; (R)-sulfolactate:NAD+ oxidoreductase; L-sulfolactate dehydrogenase; (R)-sulfolactate dehydrogenase; L-2-hydroxyacid dehydrogenase (NAD+); ComC. Cat No: EXWM-0251.
L-2-hydroxycarboxylate dehydrogenase [NAD(P)+]
The enzyme from the archaeon Methanocaldococcus jannaschii catalyses the reversible oxidation of (2R)-3-sulfolactate and (S)-malate to 3-sulfopyruvate and oxaloacetate, respectively (note that (2R)-3-sulfolactate has the same stereochemical configuration as (2S)-2-hydroxycarboxylates). The enzyme can use both NADH and NADPH, although activity is higher with NADPH. The oxidation of (2R)-3-sulfolactate was observed only in the presence of NADP+. The same organism also possesses an NAD+-specific enzyme with similar activity, cf. EC 1.1.1.337, L-2-hydroxycarboxylate dehydrogenase (NAD+). Group: Enzymes. Synonyms: MdhII; lactate/malate dehydrogenase. Enzyme Commission Number: EC 1.1.1.375. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0293; L-2-hydroxycarboxylate dehydrogenase [NAD(P)+]; EC 1.1.1.375; MdhII; lactate/malate dehydrogenase. Cat No: EXWM-0293.
L-2-hydroxyglutarate dehydrogenase
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with other acceptors. The systematic name of this enzyme class is (S)-2-hydroxyglutarate:acceptor 2-oxidoreductase. Group: Enzymes. Synonyms: α-ketoglutarate reductase; α-hydroxyglutarate dehydrogenase; L-α-hydroxyglutarate dehydrogenase; hydroxyglutaric dehydrogenase; α-hydroxyglutarate oxidoreductase; L-α-hydroxyglutarate:NAD+ 2-oxidoreductase; α-hydroxyglutarate dehydrogenase (NAD+ specific); (S)-2-hydroxyglutarate:(acceptor) 2-oxidoreductase. Enzyme Commission Number: EC 1.1.99.2. CAS No. 9028-80-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0449; L-2-hydroxyglutarate dehydrogenase; EC 1.1.99.2; 9028-80-2; α-ketoglutarate reductase; α-hydroxyglutarate dehydrogenase; L-α-hydroxyglutarate dehydrogenase; hydroxyglutaric dehydrogenase; α-hydroxyglutarate oxidoreductase; L-α-hydroxyglutarate:NAD+ 2-oxidoreductase; α-hydroxyglutarate dehydrogenase (NAD+ specific); (S)-2-hydroxyglutarate:(acceptor) 2-oxidoreductase. Cat No: EXWM-0449.
L-2-Hydroxyglutaric Acid
L-2-Hydroxyglutaric Acid. CAS No. 13095-48-2. Product ID: ACM13095482. Molecular formula: C5H8O5. Mole weight: 148.11. Alfa Chemistry - ISO 9001:32057 Certified.
L-2-Hydroxyglutaric acid disodium
L-2-Hydroxyglutaric acid disodium is an epigenetic modifier and putative oncometabolite in renal cancer. L-2-Hydroxyglutaric acid disodium can inhibit histone demethylases and hence promote histone methylation[1]. L-2-Hydroxyglutaric acid inhibits mitochondrial creatine kinase (Mi-CK) activity with Km and Ki of 2.52 mM and 11.13 mM, respectively[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-2-Hydroxyglutaric acid disodium. CAS No. 63512-50-5. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W015114.
L-2-Hydroxyglutaric acid disodium (Standard)
L-2-Hydroxyglutaric acid (disodium) (Standard) is the analytical standard of L-2-Hydroxyglutaric acid (disodium). This product is intended for research and analytical applications. L-2-Hydroxyglutaric acid disodium is an epigenetic modifier and putative oncometabolite in renal cancer. L-2-Hydroxyglutaric acid disodium can inhibit histone demethylases and hence promote histone methylation[1]. L-2-Hydroxyglutaric acid inhibits mitochondrial creatine kinase (Mi-CK) activity with Km and Ki of 2.52 mM and 11.13 mM, respectively[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-2-Hydroxyglutaric acid disodium (Standard). CAS No. 63512-50-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W015114R.
Phenylglycine. CAS No. 2935-35-5. Categories: l-phenylglycine.
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L-(+)-2-Phenylglycine-d5
Labeled L-Phenylglycine. Group: Biochemicals. Alternative Names: (αS)-α-Amino-benzeneacetic-d5 Acid; L-2-Phenyl-glycine-d5; (+)-(S)-Phenylglycine-d5; (+)-Phenylglycine-d5; (2S)-Amino-2-phenylethanoic-d5 Acid. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
L-(+)-2-Phenylglycine-[d5]
L-(+)-2-Phenylglycine-[d5] is a labelled L-α-Phenyl-glycine, which is a metabolite of glycine. Synonyms: L-(+)-2-Phenylglycine-d5; (+)-Phenylglycine-d5; L-2-Phenyl-glycine-d5; (+)-(S)-Phenylglycine-d5; (2S)-Amino-2-phenylethanoic-d5 Acid. Grade: 95% by HPLC; 98% atom D. CAS No. 1246820-68-7. Molecular formula: C8H4D5NO2. Mole weight: 156.2.
L2 Polyethylene Packaging Profile
Offering valuable protection for glass, appliances, furniture, windows, and even used in garage doors, our polyethylene packaging profiles have a plethora of uses to protect your valuables. Simply purchase the channel you need in any size, and you will be able to adequately protect your belongings during a move. Moving is not a delicate process, and we want to protect your things with our polyethylene packaging profiles; their foam base will protect from breaking, scratches, and nicks.
An intermediate in the synthesis of Perindopril. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
L-(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid benzyl ester tosylate salt
L-(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid benzyl ester tosylate salt. Group: Biochemicals. Alternative Names: [2S-(2a,3a-b,7a-b)]-Octahydro-1H-indole-2-carboxylic acid phenylmethyl ester tosylate salt. Grades: Highly Purified. CAS No. 904062-52-9. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C23H29NO5S. US Biological Life Sciences.
Worldwide
L319
L319 is an ionizable cationic lipidoid and can be used for synthetic liposomes, from the patent WO-2011153493-A2, compound 1[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Di((Z)-Non-2-en-1-yl) 9-((4-(dimethylamino)butanoyl)oxy)heptadecanedioate. CAS No. 1351586-50-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139298.
L-3,5-Diiodotyrosine methyl ester hydrochloride. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
L-364,373
L-364,373. Group: Biochemicals. Grades: Purified. CAS No. 103342-82-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
L-364,373
L-364,373 (R-L3) is a voltage-gated Kv7.1 (KCNQ1)/mink channels activator. L-364,373 activates Iks (slow delayed rectifier potassium current) and shortens action potential duration in guinea pig cardiac myocytes, and suppresses early afterdepolarizations in rabbit ventricular myocytes[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: R-L3. CAS No. 103342-82-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-108591.
L-365260
L-365260 is an orally active and selective antagonist of non-peptide gastrin and brain cholecystokinin receptor (CCK-B), with Kis of 1.9 nM and 2.0 nM, respectively. L-365260 interacts in a stereoselective and competitive manner with guinea pig stomach gastrin and brain CCK receptors. L-365260 can enhance Morphine analgesia and prevents Morphine tolerance[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 118101-09-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106840.
L-365,260
L-365,260. Group: Biochemicals. Grades: Purified. CAS No. 118101-09-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
L-368,899 hydrochloride
L-368,899 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 160312-62-9. Pack Sizes: 1mg, 10mg. US Biological Life Sciences.
Worldwide
L-368,899 hydrochloride
L-368,899 hydrochloride is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist, with IC50s of 8.9 nM and 26 nM for rat uterus and human uterus oxytocin receptor, respectively. L-368,899 hydrochloride used as a tocolytic agent[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 160312-62-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108677.
L-371,257
L-371,257. Group: Biochemicals. Grades: Purified. CAS No. 162042-44-6. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
L-3-Amino methyl phenylalanine
L-3-Amino methyl phenylalanine. Group: Biochemicals. Alternative Names: (2S) -2-Amino-3-[3- (aminomethyl) phenyl]propanoic acid. Grades: Highly Purified. CAS No. 57213-47-5. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
L-3-Amino methyl phenylalanine 98+%
L-3-Amino methyl phenylalanine 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences.