A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
DL-a-Aminosuberic acid 98+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 3054-7-7. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
DLAC
Non-ionic Detergents. Alternative Names: N-decyl-4-O-β-D-galactopyranosyl-D-gluconamide. CAS No. 70803-56-4. Molecular formula: C22H43NO11. Mole weight: 497.6. Appearance: Powder. Purity: ≥97%. IUPACName: (2R,3R,4R,5R)-N-decyl-2,3,5,6-tetrahydroxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanamide.
D-Lactal
D-Lactal is a vital ingredient commonly used in the biomedical industry for various applications. It plays a significant role in the treatment of liver diseases, particularly in promoting the regeneration of damaged liver cells. Moreover, D-Lactal is utilized in the formulation of drugs targeting gastrointestinal disorders, aiding in reducing inflammation and enhancing gut health. Synonyms: (2R,3R,5R)-4-((1R,2R,3S,4S,5R)-1,2,3,4,5,6-hexahydroxyhexyloxy)-2,3,5,6-tetrahydroxyhexanal. CAS No. 65207-55-8. Molecular formula: C12H20O9. Mole weight: 308.28.
D-lactate-2-sulfatase
Highly specific. Group: Enzymes. Synonyms: (S)-2-O-sulfolactate 2-sulfohydrolase (incorrect stereochemistry). Enzyme Commission Number: EC 3.1.6.17. CAS No. 93586-05-1. 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-3750; D-lactate-2-sulfatase; EC 3.1.6.17; 93586-05-1; (S)-2-O-sulfolactate 2-sulfohydrolase (incorrect stereochemistry). Cat No: EXWM-3750.
D-lactate dehydratase
The enzyme converts methylglyoxal to D-lactate in a single glutathione (GSH)-independent step. The other known route for this conversion is the two-step GSH-dependent pathway catalysed by EC 4.4.1.5 (lactoylglutathione lyase) and EC 3.1.2.6 (hydroxyacylglutathione hydrolase). Group: Enzymes. Synonyms: glyoxylase III. Enzyme Commission Number: EC 4.2.1.130. 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-4971; D-lactate dehydratase; EC 4.2.1.130; glyoxylase III. Cat No: EXWM-4971.
D-lactate dehydrogenase
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. Group: Enzymes. Synonyms: lactic acid dehydrogenase; lactic acid dehydrogenase; D-specific lactic dehydrogenase; D-(-)-lactate dehydrogenase (NAD); D-lactic acid dehydrogenase; D-lactic dehydrogenase. Enzyme Commission Number: EC 1.1.1.28. CAS No. 9028-36-8. D-LDH. 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-0187; D-lactate dehydrogenase; EC 1.1.1.28; 9028-36-8; lactic acid dehydrogenase; lactic acid dehydrogenase; D-specific lactic dehydrogenase; D-(-)-lactate dehydrogenase (NAD); D-lactic acid dehydrogenase; D-lactic dehydrogenase. Cat No: EXWM-0187.
D-lactate dehydrogenase (acceptor)
The zinc flavoprotein (FAD) from the archaeon Archaeoglobus fulgidus cannot utilize NAD+, cytochrome c, methylene blue or dimethylnaphthoquinone as acceptors. In vitro it is active with artificial electron acceptors such as 2,6-dichlorophenolindophenol, but the physiological acceptor is not yet known. Group: Enzymes. Synonyms: D-2-hydroxy acid dehydrogenase; D-2-hydroxy-acid dehydrogenase; (R)-2-hydroxy-acid:acceptor 2-oxidoreductase. Enzyme Commission Number: EC 1.1.99.6. CAS No. 9028-83-5. 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-0469; D-lactate dehydrogenase (acceptor); EC 1.1.99.6; 9028-83-5; D-2-hydroxy acid dehydrogenase; D-2-hydroxy-acid dehydrogenase; (R)-2-hydroxy-acid:acceptor 2-oxidoreductase. Cat No: EXWM-0469.
D-lactate dehydrogenase (cytochrome)
A flavoprotein (FAD). Group: Enzymes. Synonyms: lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D-(-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D-(-)-lactic cytochrome c reductase. Enzyme Commission Number: EC 1.1.2.4. CAS No. 37250-79-6. 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-0386; D-lactate dehydrogenase (cytochrome); EC 1.1.2.4; 37250-79-6; lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D-(-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D-(-)-lactic cytochrome c reductase. Cat No: EXWM-0386.
D-lactate dehydrogenase (cytochrome c-553)
The enzyme from the sulfate-reducing bacterium Desulfovibrio vulgaris can also act on (R)-2-hydroxybutanoate. Group: Enzymes. Enzyme Commission Number: EC 1.1.2.5. CAS No. 37250-79-6. 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-0387; D-lactate dehydrogenase (cytochrome c-553); EC 1.1.2.5; 37250-79-6. Cat No: EXWM-0387.
D-Lactate dehydrogenase from Bacteria, Recombinant
In enzymology, a D-lactate dehydrogenase is an enzyme that catalyzes the chemical reaction: (D)-lactate + 2 ferricytochrome c<-> pyruvate + 2 ferrocytochrome c. Thus, the two substrates of this enzyme are (D)-lactate and ferricytochrome c, whereas its two products are pyruvate and ferrocytochrome c. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with a cytochrome as acceptor. This enzyme participates in pyruvate metabolism. It employs one cofactor, FAD. Group: Enzymes. Synonyms: EC 1.1.1.28; D-Lactic Dehydrogenase; 9028-36-8; (D)-lactate:ferricytochrome-c 2-oxidoreductase; lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D-(-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D-(-)-lactic cytochrome c reductase. Enzyme Commission Number: EC 1.1.1.28. CAS No. 9028-36-8. D-LDH. Mole weight: 44 kD (SDS-PAGE). Activity: > 800 U/mg Protein. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Bacteria. EC 1.1.1.28; D-Lactic Dehydrogenase; 9028-36-8; (D)-lactate:ferricytochrome-c 2-oxidoreductase; lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D-(-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D-(-)-lactic cytochrome c reductase. Cat No: NATE-1042.
D-lactate Dehydrogenase from E. coli, Recombinant
In enzymology, a D-lactate dehydrogenase is an enzyme that catalyzes the chemical reaction: (D)-lactate + 2 ferricytochrome c<-> pyruvate + 2 ferrocytochrome c. Thus, the two substrates of this enzyme are (D)-lactate and ferricytochrome c, whereas its two products are pyruvate and ferrocytochrome c. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with a cytochrome as acceptor. This enzyme participates in pyruvate metabolism. It employs one cofactor, FAD. This protein is fused with 6x his tag at n terminus and the protein has a calculated mw of 39.1 kda (353aa). Group: Enzymes. Synonyms: EC 1.1.1.28; D-Lactic Dehydrogenase; 9028-36-8; (D)-lactate:ferricytochrome-c . Enzyme Commission Number: EC 1.1.1.28. Purity: > 95% by SDS-PAGE. D-LDH. Mole weight: 39.1 kDa. Activity: > 200 units/mg. Storage: Store at +4°C for short term (1-2 weeks). For long term storage, aliquot and store at -70°C. Avoid repeated freeze/thaw cycles. Form: Liquid. Source: E. coli. EC 1.1.1.28; D-Lactic Dehydrogenase; 9028-36-8; (D)-lactate:ferricytochrome-c 2-oxidoreductase; lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D- (-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D- (-)-lactic cytochrome c reductase; D-lactate Dehydrogenase. Cat No: NATE-1654.
D-Lactate dehydrogenase, Microorganism
D-Lactate dehydrogenase, Microorganism (D-LDH) is an oxidoreductase that uses NAD + or NADP + as an acceptor and acts on the donor CH-OH group, and can catalyze the oxidation of D-lactate to pyruvate. D-Lactate dehydrogenase widely exists in bacteria and fungi, and is often used in biochemical research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: D-LDH. CAS No. 9028-36-8. Pack Sizes: 500 U; 1 KU. Product ID: HY-P2897.
D-Lactic acid 92+%
D-Lactic acid 92+%. Group: Biochemicals. Alternative Names: (R)-2-Hydroxypropionic acid; D-(R)-2-Hydroxypropionic acid; D-2-Hydroxypropanoic acid. Grades: Highly Purified. CAS No. 10326-41-7. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. US Biological Life Sciences.
Worldwide
D-Lactic acid 99+% (TLC)
D-Lactic acid 99+% (TLC). Group: Biochemicals. Alternative Names: (R)-2-Hydroxypropionic acid; D-(R)-2-Hydroxypropionic acid; D-2-Hydroxypropanoic acid. Grades: Reagent Grade. CAS No. 10326-41-7. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
D-(-)-Lactic acid lithium salt
100mg Pack Size. Group: Biochemicals, Building Blocks, Chiral Compounds, Salts. Formula: C3H5O3 ·Li. CAS No. 27848-81-3. Prepack ID 47196772-100mg. Molecular Weight 96.01. See USA prepack pricing.
D-(-)-Lactic acid sodium
D-(-)-Lactic acid ((R)-2-Hydroxypropionic acid ) sodium is an endogenous metabolite. Uses: Scientific research. Group: Natural products. Alternative Names: (R)-2-Hydroxypropionic acid sodium. CAS No. 920-49-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111095B.
D-(+)-Lactide
D-(+)-Lactide is the cyclic di-ester of lactic acid (L113490), an by product that is produced by muscle cells and red blood cells when the body breaks down carbohydrates for energy during times of low oxygen levels. Lactide can be polymerized to polylactic acid using a suitable catalyst go give materials of useful properties. Group: Biochemicals. Grades: Highly Purified. CAS No. 13076-17-0. Pack Sizes: 100mg, 500mg. Molecular Formula: C6H8O4. US Biological Life Sciences.
D-Lactose monohydrate. Synonyms: β-D-Gal-(1→4)-D-Glc, 4-O-β-D-Galactopyranosyl-D-glucose, Milk sugar. CAS No. 64044-51-5. Product ID: PE-0228. Molecular formula: C12H22O11 · H2O. Category: Diluent Excipients. Product Keywords: Pharmaceutical Excipients; Diluent Excipients; D-Lactose monohydrate; PE-0228; 64044-51-5; C12H22O11·H2O; 200-559-2; MFCD00166994; 64044-51-5. Purity: ≥99.5% (HPLC). EC Number: 200-559-2. Physical State: Solid. Solubility: H2O: 0.5 M at 20 °C, clear, colorless. Quality Level: 100. Application: D-Lactose is a disaccharide of D-glucose and D-galactose units found as a major sugar in milk. D-Lactose is used for the culture of lactic acid metabolizing bacteria, lactic acid bacteria. D-Lactose is used to identify and characterized galectins.
D-Lactose monohydrate
It is widely used as a carrier, diluent, and flow aid in dry powder inhalation formulations. Synonyms: Inhalation lactose (lactose monohydrate, open form); Gal1-b-4Glc; 4-O-β-D-Galactopyranosyl-D-glucose Monohydrate; Dilactose S; Lactose Monohydrate; Microtose; Pharmatose; Respitose; 4-O-b-D-Galactopyranosyl-D-glucopyranose monohydrate; b-D-Gal-(1,4)-D-Glc monohydrate; d-(+)-lactose monohydrate. Grades: ≥95%. CAS No. 64044-51-5. Molecular formula: C12H22O11.H2O. Mole weight: 360.31.
D(+)-Lactose monohydrate
1kg Pack Size. Group: Carbohydrates, Sugars. Formula: C12H22O11 ·H2O. CAS No. 10039-26-6. Prepack ID 17095289-1kg. Molecular Weight 360.31. See USA prepack pricing.
DL-Adrenaline
DL-Adrenaline is a hormone and a neurotransmitter secreted by the medulla of the adrenal glands. Synonyms: DL-Adrenaline; DL Adrenaline; Racepinefrine; Racepinephrine; DL-Epinephrine; DL Epinephrine; (+/-)-Adrenaline; rac Epinephrine. Grades: >98%. CAS No. 329-65-7. Molecular formula: C9H13NO3. Mole weight: 183.2.
D,L-Adrenochrome
D,L-Adrenochrome. Group: Biochemicals. Alternative Names: 3-Hydroxy-1-methyl-5,6-indolinedione,2,3-dihydro-3-hydroxy-1-methyl-1H-indole-5,6-dione. Grades: Highly Purified. CAS No. 54-06-8. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C9H9NO3. US Biological Life Sciences.
The substance mainly responsible for the red colors produced during the mild oxidation of adrenaline. Group: Biochemicals. Alternative Names: 3-Hydroxy-1-methyl-5,6-indolinedione; 2,3-Dihydro-3-hydroxy-1-methyl-1H-indole-5,6-dione. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
DL-Ala-Gly-OH 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 2.5g. US Biological Life Sciences.
Worldwide
DL-Alanine
DL-alanine, an orally active amino acid , is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. Alternative Names: DL-2-Aminopropionic acid. CAS No. 302-72-7. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-N2362.
DL-Alanine
DL-Alanine. Group: Biochemicals. Grades: Highly Purified. CAS No. 302-72-7. Pack Sizes: 1kg, 2kg, 5kg. Molecular Formula: C3H7NO2. US Biological Life Sciences.
Worldwide
DL-Alanine
DL-Alanine, a racemic mixture of D- and L-alanine, is used as a model reagent for development of amino acid racemic resolution techniques. DL-Alanine is used in mixed ligand (chelate) studies with transition metals such as Cu(II), Zn(ll) and Cd(ll). Group: Amino acids. Alternative Names: (±)-2-Aminopropionic acid. CAS No. 302-72-7. Molecular formula: CH3CH(NH2)COOH. Mole weight: 89.09. Canonical SMILES: CC(N)C(O)=O. ECNumber: 206-126-4. Catalog: ACM302727-2.
DL-Alanine
1kg Pack Size. Group: Amino Acids. Formula: C3H7NO2. CAS No. 302-72-7. Prepack ID 44733272-1kg. Molecular Weight 89.09. See USA prepack pricing.
DL-Alanine
Alanine (abbreviated as Ala or A; encoded by the codons GCU, GCC, GCA, and GCG) is an α-amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated -NH3+ form under biological conditions), an α-carboxylic acid group (which is in the deprotonated -COO- form under biological conditions), and a side chain methyl group, classifying it as a nonpolar (at physiological pH), aliphatic amino acid. It is non-essential in humans, meaning the body can synthesize it.The L-isomer (left-handed) of alanine is one of the 20 amino acids encoded by the human genetic code. L-Alanine is second only to leucine in rate of occurrence, accounting for 7.8% of the primary structure in a sample of 1,150 proteins. The right-handed form, D-Alanine occurs in bacterial cell walls and in some peptide antibiotics. Synonyms: DL-Ala-OH; (R,S)-2-Aminopropionic acid. Grades: 98.5-101.0% (Assay by titration). CAS No. 302-72-7. Molecular formula: C3H7NO2. Mole weight: 89.09.
DL-Alanine
DL-Alanine is a racemic mixture of alanine, a non-essential alpha-amino acid. Alanine is one of the most common residues for protein synthesis and is involved in the metabolism of tryptophan and vitamin pyridoxine. Furthermore, alanine is an important source of energy for muscles and central nervous system. It strengthens the immune system, helps in the metabolism of sugars and organic acids, and displays a cholesterol-reducing effect in animals. CAS No. 302-72-7. Product ID: PAP-0005. Molecular formula: C3H7NO2. Category: Amino acid. Product Keywords: Amino Acid Series; DL-Alanine; PAP-0005; Amino acid; C3H7NO2; 302-72-7. Color: White. EC Number: 206-126-4. Physical State: Crystals or Crystalline Powder. Solubility: H2O: soluble. Storage: Keep in dark place,Inert atmosphere,Room temperature. Applications: DL-alanine is an amino acid, a racemic compound of L- and D-alanine. DL-alanine, together with aqueous silver nitrate, is used for nanoparticle generation as a reducing agent and an end-sealing agent. DL-alanine can be used for the chelation of Cu(II), Zn(II), Cd(11) and other transition metals. DL-alanine is a sweetener, placed in the same group as glycine and saccharin sodium. DL-alanine plays a key role in the glucose-alanine cycle between tissues and the liver. Boiling Point: 212.9±23.0 °C(Predicted). Melting Point: 289 °C (dec.) (lit.). Density: 1,424 g/cm3. Product Description: DL-alanine is an amino acid, a rac
DL-Alanine-13C-1
DL-Alanine- 13 C-1 is the 13 C-labeled DL-Alanine. DL-alanine, an amino acid, is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine, and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver[1][2][3][4][5][6]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: DL-2-Aminopropionic acid- 13 C-1. CAS No. 102029-81-2. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-N2362S.
DL-Alanine-13C-3
DL-Alanine- 13 C-3 is the 13 C-labeled DL-Alanine. DL-alanine, an amino acid, is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine, and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver[1][2][3][4][5][6]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: DL-2-Aminopropionic acid- 13 C-3. CAS No. 131157-42-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N2362S1.
DL-Alanine 99+%
DL-Alanine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences.
DL-Alanine ethyl ester hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 617-27-6. Pack Sizes: 50g, 100g. Molecular Formula: C5H11NO2·HCl. US Biological Life Sciences.
Worldwide
D,L-Alanine Ethyl Ester, Hydrochloride
D,L-Alanine Ethyl Ester, Hydrochloride. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5g. US Biological Life Sciences.
Worldwide
DL-Alanine ethyl ester hydrochloride 99+%
DL-Alanine ethyl ester hydrochloride 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g. US Biological Life Sciences.
Worldwide
DL-Alanine methyl ester hydrochloride
DL-Alanine methyl ester hydrochloride. Group: Biochemicals. Grades: Reagent Grade. CAS No. 13515-97-4. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences.
Worldwide
DL-Alanine Methyl Ester Hydrochloride
White crystals, hygroscopic. CAS No. 13515-97-4. Pack Sizes: 50g. Product ID: FR-0007. M.P. 157-158. Mole weight: 139.58.
Frinton Laboratories
DL-Alaninol
A reagent used in the synthesis of polyunsaturated fatty acid amides. Synonyms: H-DL-Ala-ol; (±)-2-Amino-1-propanol; 2-Aminopropan-1-ol; 2-Amino-1-propanol. Grades: 98+ %. CAS No. 6168-72-5. Molecular formula: C3H9NO. Mole weight: 75.11.
DL-Alaninol Methyl Ether
Used in the preparation of heterocyclic compounds, as integrase inhibiting antiviral agents. Group: Biochemicals. Alternative Names: (±)-1-Methoxy-2-propanamine; (±)-1-Methoxy-2-propylamine; 1-Methoxy-2-aminopropane; 1-Methoxy-2-propanamine; 1-Methoxy-2-propylamine; 1-Methoxyisopropylamine; 1-Methyl-2-methoxyethylamine; 2-Amino-1-methoxypropane; 2-Methoxy-1-methylethylamine; 2-Methoxyisopropylamine; DL-Alaninol methyl ether; Methoxyisopropylamine; [1-(Methoxy)propan-2-yl]amine. Grades: Highly Purified. CAS No. 37143-54-7. Pack Sizes: 10g. US Biological Life Sciences.
Worldwide
D,L-Alanosine
D,L-Alanosine. Group: Biochemicals. Alternative Names: 3-(Hydroxynitrosoamino)-D,L-alanine. Grades: Highly Purified. CAS No. 5854-95-5. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C3H7N3O4. US Biological Life Sciences.
Worldwide
DL-Alanosine-15N2
D,L-Alanosine-15N2 is an antibiotic substance from the fermentation of Streptomyces alanosinicus, which is an experimental insect reproduction inhibitor. Group: 15n labeled compounds. Alternative Names: 3-(Hydroxynitrosoamino)-DL-alanine-15N2. CAS No. 1219187-51-5. Molecular formula: C3H7N15N2O4. Mole weight: 151.09. Appearance: Crystalline. Canonical SMILES: NC(C[15N](O)[15N]=O)C(O)=O. Density: 1.8±0.1 g/cm3. Catalog: ACM1219187515.
An antibiotic substance. An experimental insect reproduction inhibitor. Group: Biochemicals. Alternative Names: 3-(Hydroxy-15N-nitroso-15N-amino)-D,L-alanine. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
DL-a-Lipoic acid NHS 99+% (NMR)
DL-a-Lipoic acid NHS 99+% (NMR). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
DL-allo-Isoleucine
Synonyms: DL-allo-Ile-OH; (2RS,3SR)-2-Amino-3-methylpentanoic acid; (2RS,3SR)-2-Amino-3-methylvaleric acid; DL allo Ile OH. Grades: ≥ 99% (HPLC). CAS No. 3107-4-8. Molecular formula: C6H13NO2. Mole weight: 131.17.
DL-allo-Isoleucine 99+%
DL-allo-Isoleucine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
Dl-allo-threonine
Heterocyclic Organic Compound. CAS No. 114-98-9. Purity: 0.96. Catalog: ACM114989.
Dl-Aloesol is produced from the endophytic fungus HCCB06030. Synonyms: 7-Hydroxy-2-(2'-hydroxypropyl)-5-methylchromone; DL-Aloesol; 4H-1-Benzopyran-4-one, 7-hydroxy-2-(2-hydroxypropyl)-5-methyl-. Grades: 98.5%. CAS No. 104871-04-7. Molecular formula: C13H14O4. Mole weight: 234.25.