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H7021

Sigma-Aldrich

2-Hydroxyhexadecanoic acid

≥98% (capillary GC)

Sinonimo/i:

2-Hydroxypalmitic acid, DL-α-Hydroxypalmitic acid

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About This Item

Formula condensata:
CH3(CH2)13CH(OH)COOH
Numero CAS:
764-67-0
Peso molecolare:
272.42
Numero CE:
212-129-1
Numero MDL:
MFCD00014343
Codice UNSPSC:
12352211
ID PubChem:
24895781
NACRES:
NA.25

Livello qualitativo

200

Saggio

≥98% (capillary GC)

Tipo di lipide

saturated FAs

Temperatura di conservazione

2-8°C

Stringa SMILE

CCCCCCCCCCCCCCC(O)C(O)=O

InChI

1S/C16H32O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15,17H,2-14H2,1H3,(H,18,19)
JGHSBPIZNUXPLA-UHFFFAOYSA-N

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Azioni biochim/fisiol

2-Hydroxyhexadecanoic acid (2OH-HDA) is used as a representative of the saturated long-chain hydroxyl fatty acids group, members of which have potential roles in anti-inflammatory action, neuroprotection, and bactericide and anti-cancer defense.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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2-Hydroxyisocaproic acid 99%

Sigma-Aldrich

219819

2-Hydroxyisocaproic acid

12-Hydroxystearic acid United States Pharmacopeia (USP) Reference Standard

USP

1331008

12-Hydroxystearic acid

12-Hydroxyoctadecanoic acid 99%

Sigma-Aldrich

219967

12-Hydroxyoctadecanoic acid

DL-β-Hydroxymyristic acid ≥98%

Sigma-Aldrich

H4148

DL-β-Hydroxymyristic acid

(±)-3-Hydroxydecanoic acid ≥98%

Sigma-Aldrich

H3648

(±)-3-Hydroxydecanoic acid

Ricinoleic acid ≥95%

Sigma-Aldrich

R7257

Ricinoleic acid

Elena E Pohl et al.
Biochimica et biophysica acta, 1778(5), 1292-1297 (2008-03-04)
Hydroxyl group-containing fatty acids play an important role in anti-inflammatory action, neuroprotection, bactericide and anti-cancer defense. However, the mechanism of long-chain hydroxy fatty acids (HFA) transport across plasma membranes is still disputed. Two main hypotheses have been suggested: firstly, that
Tomotake Morita et al.
Bioscience, biotechnology, and biochemistry, 75(8), 1597-1599 (2011-08-09)
Cryptococcus humicola JCM 1461 efficiently produced cellobiose lipids (CLs), bolaform biosurfactants. The main product was identified as 16-O-(2″,3″,4″,6'-tetra-O-acetyl-β-cellobiosyl)-2-hydroxyhexadecanoic acid. The production yield of CLs reached 13.1 g/L under the intermittent feeding of glucose. The critical micelle concentrations (CMC) of the
J A Hamilton
Prostaglandins, leukotrienes, and essential fatty acids, 60(5-6), 291-297 (1999-09-02)
In early research on fatty acid transport, passive diffusion seemed to provide an adequate explanation for movement of fatty acids through the membrane bilayer. This simple hypothesis was later challenged by the discovery of several proteins that appeared to be
T Kaneshiro et al.
Lipids, 28(5), 397-401 (1993-05-01)
Fumonisin B1 is a sphingolipid-like compound that enhances the accumulation of yeast sphingolipids and 2-hydroxy fatty acids. These lipids occur both as freely extractable and cell bound components in yeast fermentations. Both free and bound 2-hydroxy fatty acids produced by
S Hamanaka et al.
Biochimica et biophysica acta, 961(3), 374-377 (1988-08-12)
Monoglycosylceramides were isolated from pig epidermal cells which had been prepared free from dermal elements. The most polar glycolipid among the five isolated monoglycosylceramides was galactosylceramide. The galactosylceramide was composed of alpha-hydroxypalmitic acid and 16- and 18-carbon chain sphingenine, being
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