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19213 Results for: "cis-2,6-Dimethylpiperazine"

cis-2,6-Dimethylpiperazine 99

Supplier: Thermo Fisher Scientific

cis-2,6-Dimethylpiperazine 99

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cis-2,6-Dimethylpiperazine 98+%

Supplier: Apollo Scientific

cis-2,6-Dimethylpiperazine 98+%

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2,6-Dimethylpiperazine, Sigma-Aldrich®

Supplier: Merck

2,6-Dimethylpiperazine, Sigma-Aldrich®

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2,6-Dimethylpiperazine

Supplier: Molekula

2,6-Dimethylpiperazine

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4-(cis-3,5-Dimethylpiperazin-1-yl)-3-fluoroaniline

Supplier: Apollo Scientific

4-(cis-3,5-Dimethylpiperazin-1-yl)-3-fluoroaniline

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tert-Butyl (2R,6R)-2,6-dimethylpiperazine-1-carboxylate 95%

Supplier: Apollo Scientific

tert-Butyl (2R,6R)-2,6-dimethylpiperazine-1-carboxylate 95%

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(2S,6S)-tert-Butyl 2,6-dimethylpiperazine-1-carboxylate 97%

Supplier: Apollo Scientific

(2S,6S)-tert-Butyl 2,6-dimethylpiperazine-1-carboxylate 97%

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cis-2,6-Dimethylpiperidine 95%

Supplier: Apollo Scientific

cis-2,6-Dimethylpiperidine 95%

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cis-2,6-Dimethylmorpholine 97%

Supplier: Apollo Scientific

cis-2,6-Dimethylmorpholine 97%

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cis-2,6-Dimethylmorpholine 97

Supplier: Thermo Fisher Scientific

cis-2,6-Dimethylmorpholine 97

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cis-2,6-Dimethylmorpholine 97%

cis-2,6-Dimethylmorpholine 97%

Supplier: Thermo Fisher Scientific

cis-2,6-Dimethylmorpholine 97%

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2,6-Dimethylpiperidin (mixture of cis- and trans-isomers)

Supplier: Apollo Scientific

2,6-Dimethylpiperidin (mixture of cis- and trans-isomers)

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2,6-Dimethylpiperidin (mixture of cis- and trans-isomers) predominantly cis 99%

Supplier: Thermo Fisher Scientific

Used as a base for the isolation of naturally-occurring carboxylic acids as their crystalline salts

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2,6-Dichloro-4-iodopyridine 97

Supplier: Thermo Fisher Scientific

2,6-Dichloro-4-iodopyridine 97

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2,6-Dichloro-4-iodopyridine 98%

Supplier: Apollo Scientific

2,6-Dichloro-4-iodopyridine 98%

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trans,cis-2,6-Nonadienal 90 remainder mainly trans,trans-isomer

Supplier: Thermo Fisher Scientific

trans,cis-2,6-Nonadienal 90 remainder mainly trans,trans-isomer

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cis-4-Cyclopentene-1,3-diol

Supplier: Apollo Scientific

cis-4-Cyclopentene-1,3-diol

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Citral cis- and trans-mixture 95%

Citral cis- and trans-mixture 95%

Supplier: Thermo Fisher Scientific

Citral cis- and trans-mixture 95%

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cis-4-Cyclohexene-1,2-dicarboxylic acid 98

Supplier: Thermo Fisher Scientific

cis-4-Cyclohexene-1,2-dicarboxylic acid 98

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cis-4-Aminocyclohexanol hydrochloride 97%

Supplier: Apollo Scientific

cis-4-Aminocyclohexanol hydrochloride 97%

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cis-(6-Hydroxymethyl-cyclohex-3-enyl)-carbamic acid tert-butyl ester

Supplier: Apollo Scientific

cis-(6-Hydroxymethyl-cyclohex-3-enyl)-carbamic acid tert-butyl ester

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Ponceau Xylidine ≥60 % (dye content), Sigma-Aldrich®

Supplier: SIGMA ALDRICH MICROSCOPY

Ponceau Xylidine has been used as part of the Goldner’s trichome stain to stain thin sections. It has also been used to prepare Fuchsin-Ponceau solution to stain an amyotrophic lateral sclerosis tissue-engineered

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Citral cis- and trans- mixture 95%

Supplier: Thermo Fisher Scientific

Citral cis- and trans- mixture 95%

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cis-4-Cyclohexene-1,2-dicarboxylic acid 95%

Supplier: Apollo Scientific

cis-4-Cyclohexene-1,2-dicarboxylic acid 95%

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Nerol 97

Supplier: Thermo Fisher Scientific

Nerol 97

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Nerol 97%

Nerol 97%

Supplier: Thermo Fisher Scientific

Nerol 97%

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N-Benzylmaleimide

Supplier: Apollo Scientific

N-Benzylmaleimide

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Ponceau Xylidine, pure

Ponceau Xylidine, pure

Supplier: Thermo Fisher Scientific

CAS No.: 3761-53-3

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Anti-CD33 Rabbit Polyclonal Antibody (Cy5®)

Supplier: Bioss

Putative adhesion molecule of myelomonocytic-derived cells that mediates sialic-acid dependent binding to cells. Preferentially binds to alpha-2,6-linked sialic acid (By similarity). The sialic acid recognition site may be masked by cis interactions with sialic acids on the same cell surface.

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Anti-CD33 Rabbit Polyclonal Antibody (Cy3®)

Supplier: Bioss

Putative adhesion molecule of myelomonocytic-derived cells that mediates sialic-acid dependent binding to cells. Preferentially binds to alpha-2,6-linked sialic acid (By similarity). The sialic acid recognition site may be masked by cis interactions with sialic acids on the same cell surface.

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