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Product Image Model- Price Item Name
(+)-(4,6-O-Benzylidene)methyl-alpha-D-glucopyranoside ST001459 ST001459 $61.00

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(+)-(4,6-O-Benzylidene)methyl-alpha-D-glucopyranoside ST001459

3162967

MFCD00370563

C14H18O6

282.29


IDENTIFIER
IDNUMBERNAMECASMDL
ST001459(+)-(4,6-O-Benzylidene)methyl-alpha-D-glucopyranoside3162-96-7MFCD00370563
IUPACNAME
2-methoxy-6-phenyl-2H-3,4,5,6,7,8,4a,8a-octahydro-5,7-dioxachromene-3,4-diol
Smiles
c1ccc(C2OC3C(C(O)C(OC3CO2)OC)O)cc1
Chem-Physical
FormulaMolecular WeightSALT
C14H18O6282.29
LogPLogSLipinskyAcceptors
-1-2.8246
DonorsRotation BondsChiral CentersN+O
2366
SOURCE
Derivative of glucose - natural carbohydrate
REFERENCE

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(+)-6-Aminopenicillanic acid ST055519 ST055519 $61.00

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(+)-6-Aminopenicillanic acid ST055519

551-16-6

MFCD03225429

C8H12N2O3S

216.26


IDENTIFIER
IDNUMBERNAMECASMDL
ST055519(+)-6-Aminopenicillanic acid551-16-6MFCD03225429
IUPACNAME
(2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carb oxylic acid
Smiles
N12C(SC([C@@H]2C(=O)O)(C)C)C(C1=O)N
Chem-Physical
FormulaMolecular WeightSALT
C8H12N2O3S216.26
LogPLogSLipinskyAcceptors
-0.89-2.3443
DonorsRotation BondsChiral CentersN+O
3135
SOURCE
Obtained from cultures of Penicillium chrysogenum
REFERENCE
Merck 13, 457

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(+)-alpha-Tocopherol acid succinate ST075423 ST075423 $61.00

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(+)-alpha-Tocopherol acid succinate ST075423

MFCD00198020

C33H54O5

530.79


IDENTIFIER
IDNUMBERNAMECASMDL
ST075423(+)-alpha-Tocopherol acid succinate893081MFCD00198020
IUPACNAME
3-{[(2R)-2-((4R,8R)-4,8,12-trimethyltridecyl)-2,5,7,8-tetramethylchroman-6-yl] oxycarbonyl}propanoic acid
Smiles
Cc1c2c(c(c(c1C)OC(CCC(=O)O)=O)C)CC[C](O2)(CCC[C@@H](CCC[C@@H](CCCC(C)C)C)C)C
Chem-Physical
FormulaMolecular WeightSALT
C33H54O5530.79
LogPLogSLipinskyAcceptors
12.27-8.2325
DonorsRotation BondsChiral CentersN+O
11835
SOURCE
Naturally occurring form of vitamin E; Richest sources are green vegetables, grains, and oils, particularly palm, safflower and sunflower oils. Isoln from wheat germ
REFERENCE
Merck 13, 9571

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(+)-Bicuculline ST057559 ST057559 $61.00

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(+)-Bicuculline ST057559

485494

MFCD00067279

C20H17NO6

367.36


IDENTIFIER
IDNUMBERNAMECASMDL
ST057559(+)-Bicuculline485-49-4MFCD00067279
IUPACNAME
(6R)-6-((5S)-6-methyl(5,6,7,8-tetrahydro-2H-1,3-dioxolano[4,5-g]isoquinolin-5- yl))-6-hydro-2H-1,3-dioxoleno[4,5-e]isobenzofuran-8-one
Smiles
c12c(c3C(O[C@H](c3cc2)([C@@H]2(c3cc4OCOc4cc3CCN2C)))=O)OCO1
Chem-Physical
FormulaMolecular WeightSALT
C20H17NO6367.36
LogPLogSLipinskyAcceptors
2.62-4.3446
DonorsRotation BondsChiral CentersN+O
0127
SOURCE
found in Dicentra cucullaria (L.) Bernh., Adlumia fungosa (Ait.) Greene, Fumariaceae, and several Corydalis species
REFERENCE
Merck 13, 1207

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(+)-Chelidonine monohydrate ST057180 ST057180 $61.00

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(+)-Chelidonine monohydrate ST057180

MFCD00266443

C20H19NO5

353.37


IDENTIFIER
IDNUMBERNAMECASMDL
ST057180(+)-Chelidonine monohydrate476-32-4MFCD00266443
IUPACNAME
13-methyl-6,7,13,14,12b,5b-hexahydro-2H,10H-1,3-dioxolano[4'',5''-8',7']phenan thridino[4',3'-2,1]benzo[4,5-d]1,3-dioxolen-6-ol
Smiles
c12c(C3C(N(C)C1)c1cc4OCOc4cc1CC3O)ccc1OCOc21
Chem-Physical
FormulaMolecular WeightSALT
C20H19NO5353.37
LogPLogSLipinskyAcceptors
2.14-4.1245
DonorsRotation BondsChiral CentersN+O
1136
SOURCE
Hexahydrobenzophenanthridine alkaloid. Occurs in nature in (+)-form, (-)-form and racemic form. Isoln of (+)-form from root of Chelidonium majus L., Stylophorum diphyllum (Michx.) Nutt., and Dicranostigma franchetianum (Prain) Fedde, Papaveraceae
REFERENCE
Merck 13, 2061

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(+)-Cinchonine ST056305 ST056305 $61.00

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(+)-Cinchonine ST056305

118-10-5

MFCD00180253

C19H22N2O

294.4


IDENTIFIER
IDNUMBERNAMECASMDL
ST056305(+)-Cinchonine118-10-5MFCD00180253
IUPACNAME
((5R)-5-vinylquinuclidin-2-yl)(1S)-4-quinolylmethan-1-ol
Smiles
c1(ccnc2c1cccc2)[C@@H]([C@H]1(CC2CC[N@@]1C[C@@H]2(C=C)))O
Chem-Physical
FormulaMolecular WeightSALT
C19H22N2O294.4HCl, H2O
LogPLogSLipinskyAcceptors
3.56-4.5341
DonorsRotation BondsChiral CentersN+O
1343
SOURCE
Occurs in most varieties of cinchona bark, especially in bark of Cinchona micrantha, Rubiaceae
REFERENCE
Merck 13, 2308

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(+)-Dehydroabietylamine ; Leelamine ST056281 ST056281 $61.00

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(+)-Dehydroabietylamine ; Leelamine ST056281

1446-61-3

MFCD05618226

C20H31N

285.47


IDENTIFIER
IDNUMBERNAMECASMDL
ST056281(+)-Dehydroabietylamine ; Leelamine1446-61-3MFCD05618226
IUPACNAME
[(4aS,1R,10aR)-1,4a-dimethyl-7-(methylethyl)-1,2,3,4,9,10,10a,4a-octahydrophen anthryl]methylamine
Smiles
c12[C]3(C(C(CN)(C)CCC3)CCc1cc(cc2)C(C)C)C
Chem-Physical
FormulaMolecular WeightSALT
C20H31N285.47
LogPLogSLipinskyAcceptors
7.19-5.5530
DonorsRotation BondsChiral CentersN+O
2131
SOURCE
a main ingredient of rosin amine, isolated from Rosin Gum
REFERENCE

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(+)-Emetine dihydrochloride hydrate ST056340 ST056340 $61.00

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(+)-Emetine dihydrochloride hydrate ST056340

316-42-7

MFCD04220906

C29H40N2O4

480.65


IDENTIFIER
IDNUMBERNAMECASMDL
ST056340(+)-Emetine dihydrochloride hydrate313222-95-6
IUPACNAME
(1R)-1-[((10S,11aS,9R)-9-ethyl-2,3-dimethoxy(5,6,7,11a-tetrahydropiperidino[2, 1-a]isoquinolin-10-yl))methyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline, c hloride, hydrate
Smiles
c12[C@H]3(N(CC([C@H](C[C@@H]4(c5cc(c(OC)cc5CCN4)OC))C3)CC)CCc2cc(OC)c(c1)OC).Cl.O
Chem-Physical
FormulaMolecular WeightSALT
C29H43ClN2O5535.12
LogPLogSLipinskyAcceptors
5.49-5.9535
DonorsRotation BondsChiral CentersN+O
3647
SOURCE
Derivative of Emetine, which is principal alkaloid of ipecac, the ground roots of Uragoga ipecacuanha
REFERENCE
Merk 13, 3591

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(+)-Isocorydine; artabotrine; luteanine ST057169 ST057169 $61.00

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(+)-Isocorydine; artabotrine; luteanine ST057169

475-67-2

MFCD01844805

C20H23NO4

341.41


IDENTIFIER
IDNUMBERNAMECASMDL
ST057169(+)-Isocorydine; artabotrine; luteanine475-67-2MFCD01844805
IUPACNAME
Smiles
c12c(C[C@H]3(c4c1c(c(cc4CCN3C)OC)OC))ccc(c2O)OC
Chem-Physical
FormulaMolecular WeightSALT
C20H23NO4341.41
LogPLogSLipinskyAcceptors
4.13-4.6544
DonorsRotation BondsChiral CentersN+O
1415
SOURCE
From tubers of Corydalis cava (L.) Schweigg. & Korte (C. tuberosa DC., Fumariaceae); Artabotrys suaveolens Blume, Anonaceae; Papaver oreophilum Rupr.; Phoebe clemensii Allen (Lauraceae) and others
REFERENCE
Merck 13, 5180

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(+)-Penicillamine ST025231 ST025231 $61.00

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(+)-Penicillamine ST025231

MFCD00064303

C5H11NO2S

149.21


IDENTIFIER
IDNUMBERNAMECASMDL
ST025231(+)-Penicillamine52-66-4MFCD00064303
IUPACNAME
(2R)-2-amino-3-methyl-3-sulfanylbutanoic acid
Smiles
C([C@H](C(S)(C)C)N)(=O)O
Chem-Physical
FormulaMolecular WeightSALT
C5H11NO2S149.21
LogPLogSLipinskyAcceptors
-0.13-2.2642
DonorsRotation BondsChiral CentersN+O
3413
SOURCE
forms in urine with penicillin intake
REFERENCE

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