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ChemicalBook >> CAS DataBase List >>N-Acetyltyramine

N-Acetyltyramine

CAS No.
1202-66-0
Chemical Name:
N-Acetyltyramine
Synonyms
N-(4-Hydroxyphenethyl)acetamide;N-ACETYLTYRAMINE;Acetyltyramine, N-;4-(2-Acetylaminoethyl)phenol;N-(2-(4-HYDROXYPHENYL)ETHYL)-;N-Acetyltyramine, 10 mM in DMSO;N-(p-Hydroxyphenethyl)acetamide;N-[2-(4-Hydroxyphenyl)ethyl]acetamide;N-Acetyl-2-(4-hydroxyphenyl)ethaneamine;Acetamide, N-[2-(4-hydroxyphenyl)ethyl]-
CBNumber:
CB4392228
Molecular Formula:
C10H13NO2
Molecular Weight:
179.22
MDL Number:
MFCD01670887
MOL File:
1202-66-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-14 16:49:18
Product description Number Pack Size Price
N-Acetyltyramine ≥95% (LC/MS-ELSD) SMB00019 1mg $770
N-(4-Hydroxyphenethyl)acetamide A3518 1G $91
N-(4-Hydroxyphenethyl)acetamide A3518 5G $274
N-Acetyltyramine ≥95% 9001373 5mg $90
N-Acetyltyramine ≥95% 9001373 25mg $306
More product size

N-Acetyltyramine Properties

Melting point 169 °C
Boiling point 424.1±28.0 °C(Predicted)
Density 1.122±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility Soluble in DMSO
pka 10.01±0.15(Predicted)
form A solid
color Light brown to brown
Major Application metabolomics
vitamins, nutraceuticals, and natural products
InChI 1S/C10H13NO2/c1-8(12)11-7-6-9-2-4-10(13)5-3-9/h2-5,13H,6-7H2,1H3,(H,11,12)
InChIKey ATDWJOOPFDQZNK-UHFFFAOYSA-N
SMILES N(CCc1ccc(cc1)O)C(=O)C
FDA UNII BZB50E9QVY
NIST Chemistry Reference N-(p-hydroxyphenethyl) acetamide(1202-66-0)
UNSPSC Code 12352205
NACRES NA.25

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)
GHS05
Signal word  Danger
Hazard statements  H318
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xi
Risk Statements  41
Safety Statements  26-39
WGK Germany  3
HS Code  2924297099
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Dam. 1
Toxicity mouse,LD50,intravenous,> 500mg/kg (500mg/kg),BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)SKIN AND APPENDAGES (SKIN): HAIR: OTHERCARDIAC: CARDIOMYOPATHY INCLUDING INFARCTION,Acta Pharmacologica et Toxicologica. Vol. 38, Pg. 474, 1976.
NFPA 704
0
3 0

N-Acetyltyramine price More Price(44)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SMB00019 N-Acetyltyramine ≥95% (LC/MS-ELSD) 1202-66-0 1mg $770 2026-04-30 Buy
TCI Chemical A3518 N-(4-Hydroxyphenethyl)acetamide 1202-66-0 1G $91 2026-04-30 Buy
TCI Chemical A3518 N-(4-Hydroxyphenethyl)acetamide 1202-66-0 5G $274 2026-04-30 Buy
Cayman Chemical 9001373 N-Acetyltyramine ≥95% 1202-66-0 5mg $90 2026-04-30 Buy
Cayman Chemical 9001373 N-Acetyltyramine ≥95% 1202-66-0 25mg $306 2026-04-30 Buy
Product number Packaging Price Buy
SMB00019 1mg $770 Buy
A3518 1G $91 Buy
A3518 5G $274 Buy
9001373 5mg $90 Buy
9001373 25mg $306 Buy

N-Acetyltyramine Chemical Properties,Uses,Production

Uses

N-[2-(4-Hydroxyphenyl)ethyl]acetamide maintains anti-tumor properties and is derived from a marine bacterium named Streptoverticillium. Cytotoxin.

Definition

ChEBI: N-acetyltyramine is a member of the class of tyramines that is tyramine in which one of the hydrogens of the amino group is replaced by an acetyl group. It has a role as a marine metabolite, a bacterial metabolite, an Aspergillus metabolite, an animal metabolite and a quorum sensing inhibitor. It is a member of acetamides and a member of tyramines. It is functionally related to a tyramine.

Synthesis

Tyramine

51-67-2

Acetic anhydride

108-24-7

N-Acetyltyramine

1202-66-0

General Steps: 1. In a dry reaction flask, add p-hydroxyphenethylamine and an appropriate amount of anhydrous dichloromethane and stir to dissolve. 2. Place the reaction vial in an ice-water bath and cool to 0-5°C. Slowly add the acetic anhydride dropwise, controlling the rate of addition to maintain a reaction temperature of not more than 10°C. 3. After the dropwise addition is complete, remove the ice water bath, allow the reaction mixture to warm slowly to room temperature, and continue to stir the reaction for 2-3 hours. 4. Upon completion of the reaction, the reaction mixture was poured into ice water and the pH adjusted to neutral with dilute hydrochloric acid. 5. The aqueous phase was extracted with dichloromethane, the organic phases were combined and dried over anhydrous sodium sulfate. 6. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to give the crude product N-acetyltyramine. 7. The crude product can be further purified by column chromatography or recrystallization.

References

[1] Patent: US9522908, 2016, B2. Location in patent: Page/Page column 57
[2] Biochemical Pharmacology, 1998, vol. 55, # 1, p. 37 - 43
[3] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2014, vol. 53, # 1, p. 83 - 89

N-Acetyltyramine Preparation Products And Raw materials

Global( 83)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32468 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 17705817739 info@dycnchem.com China 52704 58
Hebei Chuanghai Biotechnology Co., Ltd
+86-17732866630 mina@chuanghaibio.com China 18126 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39037 58
PT CHEM GROUP LIMITED
+86-85511178; +86-85511178 peter68@ptchemgroup.com China 35425 58
GIHI CHEMICALS CO.,LIMITED
+86-571-86217390; +8618058761490 info@gihichemicals.com China 49895 58
Sichuan Biosynce Pharmatech Co., Ltd.
diane@biosynce.com China 4871 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131956 58
Henan Rane Chemical Co., Ltd.
+86-18738066252 info@ranechem.com China 3000 58

View Lastest Price from N-Acetyltyramine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-Acetyltyramine pictures 2026-07-13 N-Acetyltyramine
1202-66-0
$29.00-78.00 99.95% 10g TargetMol Chemicals Inc.
N-ACETYLTYRAMINE Acetamide, N-[2-(4-hydroxyphenyl)ethyl]- N-[2-(4-Hydroxyphenyl)ethyl]acetamide N-(2-(4-HYDROXYPHENYL)ETHYL)- 4-(2-Acetylaminoethyl)phenol N-Acetyl-2-(4-hydroxyphenyl)ethaneamine N-(p-Hydroxyphenethyl)acetamide quorum-sensing,N-Acetyltyramine,leukemia,Inhibitor,cytotoxicity,murine,inhibit,P388,Bacterial,N Acetyltyramine,cells,NAcetyltyramine Acetyltyramine, N- N-Acetyltyramine, 10 mM in DMSO N-(4-Hydroxyphenethyl)acetamide 1202-66-0
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