跳转至内容
Merck
CN

19-2190

L-甲硫氨酸

SAJ special grade, ≥98.5%

别名:

L-2-氨基-4-(甲硫基)丁酸, (S)-2-氨基-4-(甲巯基)丁酸

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:
CH3SCH2CH2CH(NH2)CO2H
化学文摘社编号:
分子量:
149.21
EC Number:
200-562-9
UNSPSC Code:
12352112
PubChem Substance ID:
Beilstein/REAXYS Number:
1722294
MDL number:
Assay:
≥98.5%
Grade:
SAJ special grade
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


grade

SAJ special grade

assay

≥98.5%

form

solid

availability

available only in Japan

dilution

(for analytical testing)

mp

284 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CSCC[C@H](N)C(O)=O

InChI

1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1

InChI key

FFEARJCKVFRZRR-BYPYZUCNSA-N



Still not finding the right product?

Explore all of our products under L-甲硫氨酸


存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



Ronald O Ball et al.
The Journal of nutrition, 136(6 Suppl), 1682S-1693S (2006-05-17)
Sulfur amino acid metabolism has been receiving increased attention because of the link to chronic diseases such as cardiovascular disease, Alzheimer's disease, and diabetes. In addition, the role of cysteine and optimal intakes for physiological substrates such as glutathione are
B Almé et al.
Journal of lipid research, 18(3), 339-362 (1977-05-01)
A method is described for quantitative analysis of bile acids in urine. Urine is acidified and bile acids are extracted on an Amberlite XAD-2 column. Bile salts are converted to acids on an Amberlyst A-15 column and are separated into
Olga Z Karicheva et al.
Nucleic acids research, 39(18), 8173-8186 (2011-07-05)
Mutations in human mitochondrial DNA are often associated with incurable human neuromuscular diseases. Among these mutations, an important number have been identified in tRNA genes, including 29 in the gene MT-TL1 coding for the tRNA(Leu(UUR)). The m.3243A>G mutation was described