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Merck

11009

Sigma-Aldrich

L-精氨酸

BioUltra, ≥99.5% (NT)

别名:

(S)-2-氨基-5-胍基戊酸

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About This Item

线性分子式:
H2NC(=NH)NH(CH2)3CH(NH2)CO2H
CAS号:
分子量:
174.20
Beilstein:
1725413
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.26

產品線

BioUltra

化驗

≥99.5% (NT)

形狀

powder or crystals

光學活性

[α]20/D +27.0±0.5°, c = 5% in 5 M HCl

雜質

insoluble matter, passes filter test
≤0.3% foreign amino acids

燃燒殘留物

≤0.05% (as SO4)

損耗

≤0.1% loss on drying, 20 °C (HV)

顏色

white

pH值

10.5-12.0 (25 °C, 0.5 M in H2O)

mp

222 °C (dec.) (lit.)

溶解度

H2O: 0.5 M at 20 °C, clear, colorless

負離子痕跡

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤100 mg/kg

正離子痕跡

Al: ≤5 mg/kg
As: ≤0.1 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

&lambda ;

0.5 M in H2O

紫外吸收

λ: 260 nm Amax: ≤0.2
λ: 280 nm Amax: ≤0.1

應用

peptide synthesis

SMILES 字串

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

InChI

1S/C6H14N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h4H,1-3,7H2,(H,11,12)(H4,8,9,10)/t4-/m0/s1

InChI 密鑰

ODKSFYDXXFIFQN-BYPYZUCNSA-N

基因資訊

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應用


  • L-Arginine-Dependent Nitric Oxide Production in the Blood of Patients with Type 2 Diabetes: A Pilot, Five-Year Prospective Study.: This study examines the role of L-Arginine in nitric oxide production in diabetic patients, proposing its potential benefits for managing vascular complications in diabetes (Stoian et al., 2024).

生化/生理作用

一氧化氮合成酶的底物,可转化为瓜氨酸和一氧化氮 (NO)。通过与一氧化氮相关的机理诱导胰岛素释放。

其他說明

对植物原生质体表现出稳定作用;蛋白质在IEF的酸碱度漂移校正;各种微生物的生长要求

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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A.W. Galston et al.
Plant Sci. Lett., 11, 69-69 (1978)
CRC Handbook of Microbiology, 4, 1-1 (1974)
H. Delice et al.
Electrophoresis '79, 165-165 (1980)
Krishnan Suresh Kumar et al.
European journal of medicinal chemistry, 45(11), 5474-5479 (2010-08-21)
A new series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-ones were prepared through Schiff base formation of 3-amino-2-phenyl quinazoline-4(3)H-one with various substituted carbonyl compounds. Their chemical structures were elucidated by spectral studies. Cytotoxicity and antiviral activity were evaluated against herpes simplex virus-1 (KOS), herpes simplex
Kaoru Kumazaki et al.
Nature, 509(7501), 516-520 (2014-04-18)
Newly synthesized membrane proteins must be accurately inserted into the membrane, folded and assembled for proper functioning. The protein YidC inserts its substrates into the membrane, thereby facilitating membrane protein assembly in bacteria; the homologous proteins Oxa1 and Alb3 have

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