ChemicalBook--->CAS DataBase List--->3211-76-5

3211-76-5

3211-76-5 Structure

3211-76-5 Structure
IdentificationMore
[Name]

L-(+)-Selenomethionine
[CAS]

3211-76-5
[Synonyms]

2-AMINO-4-(METHYLSELENO)BUTANOIC ACID
L-(+)-2-AMINO-4-(METHYLSELENO)BUTANOIC ACID
L-(+)-SELENOMETHIONINE
L-SELENOMETHIONINE
(S)-(+)-2-AMINO-4-(METHYLSELENO)BUTANOIC ACID
(S)-2-AMINO-4-(METHYLSELENO)BUTYRIC ACID
SELENO-L-METHIONINE
SELENOMETHIONINE, L-(+)-
SEMET
L(+)-SELENOMETHIONINE 99+% E.E.
(S)-2-AMINO-4-(METHYLSELENYL)BUTYRIC ACID
L(+)-Selenomethionine, ee 99+%, 99+%
Butanoic acid, 2-amino-4-(methylseleno)-, (2S)-
L-SELENOMETHIONINE SELENO-L-METHIONINE L-SE-MET-OH
L-selenomethionine (L-se-Met-OH)
BUTYRICACID,2-AMINO-4-(METHYLSELENYL)-,L-
L-SELENOMETHIONINE 0.5%
L-SELENOMETHIONINE USP
THALLIUM ETHYLSUFATE
(S)-(+)-2-Amino-4-(methylseleno)butanoic acid, (S)-2-Amino-4-(methylseleno)butyric acid, L-Selenomethionine, Seleno-L-methionine
[EINECS(EC#)]

608-705-0
[Molecular Formula]

C5H11NO2Se
[MDL Number]

MFCD00037210
[Molecular Weight]

196.11
[MOL File]

3211-76-5.mol
Chemical PropertiesBack Directory
[Appearance]

Solid
[Melting point ]

265 °C
[alpha ]

18 º (c=1, 1N HCl)
[Boiling point ]

320.8±37.0 °C(Predicted)
[refractive index ]

18 ° (C=0.5, 2mol/L HCl)
[storage temp. ]

−20°C
[solubility ]

H2O: 50 mg/mL
[form ]

powder
[pka]

2.26±0.10(Predicted)
[color ]

white to off-white
[Water Solubility ]

soluble
[Merck ]

8441
[Cosmetics Ingredients Functions]

ANTIOXIDANT
[InChI]

InChI=1S/C5H11NO2Se/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1
[InChIKey]

RJFAYQIBOAGBLC-BYPYZUCNSA-N
[SMILES]

C(O)(=O)[C@@H](N)CC[Se]C
[LogP]

0.152 (est)
[CAS DataBase Reference]

3211-76-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

T,N
[Risk Statements ]

R23/25:Toxic by inhalation and if swallowed .
R33:Danger of cumulative effects.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S20/21:When using, do not eat, drink or smoke .
S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
[RIDADR ]

UN 3283 6.1/PG 2
[WGK Germany ]

3
[RTECS ]

EK7713840
[F ]

10
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29309090
[Storage Class]

6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
[Hazard Classifications]

Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1
STOT RE 2
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sodium hydroxide-->Hydrochloric acid-->Methanol-->Diethyl ether-->Sulfuric acid-->Tetrahydrofuran-->Sodium-->N,N-Dimethylformamide-->Sodium chloride-->Acetone-->Ammonia-->Sodium bicarbonate-->Benzene-->Hydrogen peroxide-->Iodomethane-->Hydrogen bromide-->Magnesium-->Benzyl chloride-->Phosphorus pentoxide-->Selenium-->Tributyl borate-->L-Methionine-->Methyllithium
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

L-(+)-Selenomethionine(3211-76-5).msds
Hazard InformationBack Directory
[Chemical Properties]

Solid
[Uses]

A compound shown to increase expression of glutathione peroxidase
[Definition]

ChEBI: The L-enantiomer of selenomethionine.
[General Description]

Seleno-L-Methionine (SeMet), an organic form of selenium is found in Cupriavidus metallidurans.
[Biochem/physiol Actions]

Seleno-L-Methionine (SeMet) is capable of repressing atopic dermatitis (AD)-like skin lesions. It can also prevent the expression of total immunoglobulin E (IgE) and interleukin 4 (IL-4). It can cause ecotoxicity as it is absorbed by fish through diet.
[Synthesis]

L-Homoserine lactone hydrochloride

2185-03-7

Methaneselenol, sodium salt (9CI)

37773-10-7

L-Selenomethionine

3211-76-5

Under nitrogen protection, 13.75 g of L-homoserine lactone hydrochloride was mixed with 40 mL of N,N-dimethylformamide (DMF) and stirred until completely dissolved. Subsequently, 15.2 g of methyl selenate (CAS:37773-10-7) was dissolved in 20 mL of DMF and slowly added to the above reaction system. The reaction was heated and refluxed for 2 hours. Upon completion of the reaction, the pH of the reaction system was adjusted to 6.0 with aqueous acetic acid and a white solid was precipitated. The resulting solid was dissolved in a mixed solvent of water and ethanol for recrystallization to obtain L-selenomethionine. The total yield of this synthetic route was 72.11%, the chemical purity of the product was greater than 99% and the enantiomeric excess value (ee) was greater than 99%.

[References]

[1] Patent: CN106928110, 2017, A. Location in patent: Paragraph 0028; 0030
Spectrum DetailBack Directory
[Spectrum Detail]

L-Selenomethionine(3211-76-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

L(+)-Selenomethionine, ee 99+%, 99+%(3211-76-5)
[Sigma Aldrich]

3211-76-5(sigmaaldrich)
[TCI AMERICA]

L-Selenomethionine,>98.0%(T)(3211-76-5)
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