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T90344

Sigma-Aldrich

Tyramine

≥98.0%

Synonym(s):

2-(4-Hydroxyphenyl)ethylamine, 4-(2-Aminoethyl)phenol, 4-Hydroxyphenethylamine

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5 G
¥472.57
25 G
¥343.57

¥472.57

Available to ship on2025年4月27日Details

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5 G
¥472.57
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About This Item

Linear Formula:
HOC6H4CH2CH2NH2
CAS Number:
51-67-2
Molecular Weight:
137.18
Beilstein:
1099914
EC Number:
200-115-8
MDL number:
MFCD00008193
UNSPSC Code:
12352100
PubChem Substance ID:
24900582
NACRES:
NA.22

¥472.57

Available to ship on2025年4月27日Details

Request a Bulk Order

Quality Level

200

Assay

≥98.0%

bp

175-181 °C/8 mmHg (lit.)

mp

160-162 °C (lit.)

SMILES string

NCCc1ccc(O)cc1

InChI

1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2

InChI key

DZGWFCGJZKJUFP-UHFFFAOYSA-N

Gene Information

rat ... Drd2(24318)

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Show Differences

1 of 4

This Item
65390T2879V900670
酪胺 ≥98.0%

T90344

酪胺

3-甲氧基酪胺 盐酸盐 99% (AT)

65390

3-甲氧基酪胺 盐酸盐

酪胶 盐酸盐 ≥98%

T2879

酪胶 盐酸盐

酪胺 Vetec™, reagent grade, 99%

V900670

酪胺

assay

≥98.0%

assay

99% (AT)

assay

≥98%

assay

99%

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

-

bp

175-181 °C/8 mmHg (lit.)

bp

-

bp

-

bp

175-181 °C/8 mmHg (lit.)

mp

160-162 °C (lit.)

mp

212-215 °C, 213-215 °C (lit.)

mp

271-274 °C (lit.)

mp

160-162 °C (lit.)

Gene Information

rat ... Drd2(24318)

Gene Information

-

Gene Information

human ... ADORA2A(135), ADORA2B(136), ADORA3(140)

Gene Information

-

Application

  • Tyramine is extensively used in the preparation of a variety of hydrogels for biomedical applications.[1][2]
  • It is used as a key precursor in the total synthesis of (−)-mesembrine[3] and (−)-galanthamine.[4]
  • It can also be used in the preparation of tyramine-functionalized graphene quantum dots (GQDs) as fluorescence reporters for optical sensing of metabolites.[5]

Biochem/physiol Actions

Can enter catecholaminergic terminals and be released as a false transmitter.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    BCCL3777
    BCCK5829
    BCCG5676
    BCCF3845
    BCCC6853

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    Total Synthesis of (−)-Galanthamine by Remote Asymmetric Induction.
    Kodama, Sumiaki et al.
    Angewandte Chemie (International Edition in English), 43(20), 2659-2661 (2004)
    Ultrasensitive profiling of metabolites using tyramine-functionalized graphene quantum dots.
    Li N, et al.
    ACS Nano, 10(3), 3622-3629 (2016)
    Simona Distinto et al.
    European journal of medicinal chemistry, 48, 284-295 (2012-01-10)
    Monoamine oxidase B (MAO-B) is a promising target for the treatment of neurodegenerative disorders. We report the synthesis and the biological evaluation of halogenated derivatives of 1-aryliden-2-(4-phenylthiazol-2-yl)hydrazines. The fluorinated series shows interesting activity and great selectivity toward the human recombinant
    In situ forming hydrogels based on tyramine conjugated 4-Arm-PPO-PEO via enzymatic oxidative reaction.
    Park KM, et al.
    Biomacromolecules, 11(3), 706-712 (2010)
    Desymmetrization of cyclohexadienones via cinchonine derived thiourea-catalyzed enantioselective aza-Michael reaction and total synthesis of (−)-Mesembrine
    Gu Q and You S-L
    Chemical Science, 2(8), 1519-1522 (2011)
    View All Related Papers

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