Name | N-Boc-D-methionine |
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Synonyms |
D-Methionine, N-[(1,1-dimethylethoxy)carbonyl]-
N-(tert-Butoxycarbonyl)-D-methionine N-Boc-D-Methionine EINECS 226-043-7 N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-methionine BOC-D-Methionine MFCD00038256 (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid Boc-D-Met-OH Boc-L-Met-OH |
Description | Boc-D-Met-OH is a Methionine (HY-13694) derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 415.5±40.0 °C at 760 mmHg |
Melting Point | 47-50ºC |
Molecular Formula | C10H19NO4S |
Molecular Weight | 249.327 |
Flash Point | 205.1±27.3 °C |
Exact Mass | 249.103485 |
PSA | 100.93000 |
LogP | 2.15 |
Vapour Pressure | 0.0±2.1 mmHg at 25°C |
Index of Refraction | 1.500 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2930909090 |
~97% 5241-66-7 |
Literature: Merck and Co., Inc. Patent: US4863953 A1, 1989 ; |
~% 5241-66-7 |
Literature: Lyons, Anthony Q.; Pettit, Leslie D. Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1984 , p. 2305 - 2308 |
Precursor 2 | |
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DownStream 5 | |
HS Code | 2930909090 |
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Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |