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Key Documents

Altri documenti

W373605

Sigma-Aldrich

L-tirosina

FG

Sinonimo/i:

3-(4-idrossifenil)-L-alanina, Acido (S)-2-ammino-3-(4-idrossifenil)propionico

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About This Item

Formula condensata:
4-(HO)C6H4CH2CH(NH2)CO2H
Numero CAS:
60-18-4
Peso molecolare:
181.19
Numero FEMA:
3736
Beilstein:
392441
Numero CE:
200-460-4
Numero MDL:
MFCD00002606
Codice UNSPSC:
12164502
eCl@ss:
32160406
ID PubChem:
24901863
Numero Flavis:
17.022
NACRES:
NA.21

Origine biologica

corn

Grado

FG

Conformità normativa

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 173.65

Attività ottica

[α]20/D −10.6°, c = 4 in 1 M HCl

Punto di fusione

>300 °C (dec.) (lit.)

Solubilità

water: soluble 0.479 g/L at 25 °C

applicazioni

flavors and fragrances

Allergene alimentare

no known allergens

Organolettico

odorless

Stringa SMILE

N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI

1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1
OUYCCCASQSFEME-QMMMGPOBSA-N

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Descrizione generale

L-Tyrosine is an important amino acid mainly used as a dietary supplement.
L-tyrosine, an aromatic amino acid, is used common dietary supplement that has a wide range of applications in food and pharmaceutical industry. It is a precursor for preparing industrially important compounds such as 3,4-dihydroxy-L-phenylalanine (L-DOPA), melanin and p-hydroxystyrene. L-tyrosine can be synthesized by different biotechnological methods which are ecofriendly.

Altre note

Precursore aminoacidico della dopamina e di altre catecolamine

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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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L-Phenylalanine 99%, FCC

Sigma-Aldrich

W358509

L-Phenylalanine

D-Tyrosine ReagentPlus®, 99%

Sigma-Aldrich

855456

D-Tyrosine

L-Isoleucine 99%, FCC, FG

Sigma-Aldrich

W527602

L-Isoleucine

L-Phenylalanine reagent grade, ≥98%

Sigma-Aldrich

P2126

L-Phenylalanine

3,4-Dihydroxy-L-phenylalanine ≥98% (TLC)

Sigma-Aldrich

D9628

3,4-Dihydroxy-L-phenylalanine

Christine Nicole S Santos et al.
Applied and environmental microbiology, 74(4), 1190-1197 (2007-12-25)
We present the development of a simple, high-throughput screen for identifying bacterial strains capable of L-tyrosine production. Through the introduction of a heterologous gene encoding a tyrosinase, we were able to link L-tyrosine production in Escherichia coli with the synthesis
Keisuke Saito et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(19), 7690-7695 (2013-04-20)
Using quantum mechanics/molecular mechanics calculations and the 1.9-Å crystal structure of Photosystem II [Umena Y, Kawakami K, Shen J-R, Kamiya N (2011) Nature 473(7345):55-60], we investigated the H-bonding environment of the redox-active tyrosine D (TyrD) and obtained insights that help
Hideki Hara et al.
Nature immunology, 14(12), 1247-1255 (2013-11-05)
The inflammasome adaptor ASC contributes to innate immunity through the activation of caspase-1. Here we found that signaling pathways dependent on the kinases Syk and Jnk were required for the activation of caspase-1 via the ASC-dependent inflammasomes NLRP3 and AIM2.
Verena Rahm et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(4), 546-550 (2014-02-26)
Low-grade gliomas (LGGs) may harbor malignant foci, which are characterized by increased tumor cellularity and angiogenesis. We used diffusion-weighted MR imaging (apparent diffusion coefficient [ADC]) and PET with the amino acid O-(2-(18)F-fluorethyl)-L-tyrosine ((18)F-FET) to search for focal changes of diffusion
Tina Lütke-Eversloh et al.
Applied microbiology and biotechnology, 77(4), 751-762 (2007-10-31)
The aromatic amino acid L-tyrosine is used as a dietary supplement and has promise as a valuable precursor compound for various industrial and pharmaceutical applications. In contrast to chemical production, biotechnological methods can produce L-tyrosine from biomass feedstocks under environmentally
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