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(S)-(-)-二氨基丙烷二盐酸盐

(S)-(-)-二氨基丙烷二盐酸盐名称

[ CAS 号 ]:
19777-66-3

[ 中文名 ]:
(S)-(-)-二氨基丙烷二盐酸盐

[ 英文名 ]:
(S)-(-)-1,2-Diaminopropane dihydrochloride

[中文别名 ]:

[英文别名 ]:

(S)-(−)-Propylenediamine dihydrochloride
(2S)-propane-1,2-diamine dihydrochloride
1,2-Propanediamine, (2S)-, hydrochloride (1:2)
(S)-diaminopropane dihydrochloride
(S)-(-)-Diaminopropane Hydrochloride
S-(-)-1,2-diaminopropane dihydrochloride
R-(-)-1,2-propanediamine dihydrochloride
(S)-1,2-diaminopropane
(S)-1,2-propanediamine*2HCl
(S)-1,2-Diaminopropane Dihydrochloride

(S)-(-)-二氨基丙烷二盐酸盐物理化学性质

[ 沸点 ]:
215.8ºC at 760 mmHg

[ 熔点 ]:
227-229ºC

[ 分子式 ]:
C₃H₁₂Cl₂N₂

[ 分子量 ]:
147.047

[ 闪点 ]:
84.3ºC

[ 精确质量 ]:
146.037750

[ PSA ]:
52.04000

[ LogP ]:
2.29690

[ 外观性状 ]:
固体;White to Almost white powder to crystal

[ 蒸汽压 ]:
0.12mmHg at 25°C

[ 储存条件 ]:
存放于惰性气体之中;避免湿气 (吸湿)

[ 水溶解性 ]:
水溶性：可溶

(S)-(-)-二氨基丙烷二盐酸盐MSDS

(S)-(-)-二氨基丙烷二盐酸盐安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
2811.0

[ WGK德国 ]:
3

[ 危险类别 ]:
6.1

[ 海关编码 ]:
2921290000

(S)-(-)-二氨基丙烷二盐酸盐合成路线

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(S)-(-)-二氨基丙烷二盐酸盐海关

[ 海关编码 ]: 2921290000

[ 中文概述 ]:
2921290000. 其他无环多胺及其衍生物及它们的盐. 增值税率:17.0%. 退税率:9.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2921290000 other acyclic polyamines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

(S)-(-)-二氨基丙烷二盐酸盐文献

Capillary gas chromatographic determination of methylglyoxal from serum of diabetic patients by precolumn derivatization with 1,2-diamonopropane.

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 873(1) , 15-9, (2008)

Capillary gas chromatographic (GC) determination of methylglyoxal (MGo) was developed on the basis of precolumn derivatization with 1,2-diaminopropane (DAP) at pH 3. The elution was carried out on an ...

Optically active derivatives of imidazolines. alpha-Adrenergic blocking properties.

J. Med. Chem. 23 , 1232, (1980)

The synthesis and alpha-adrenergic blocking activity of a series of optically active 2,4-disubstituted imidazolines are presented. The substituted analogues of naphazoline, tolazoline, and clonidine p...

Stereochemical studies of adrenergic drugs. Optically active derivatives of imidazolines.

J. Med. Chem. 19 , 1382, (1976)

The synthesis of (R)-(+)-4-methyl-2-(1-naphthylmethyl)imidazoline hydrochloride (2) and (S)-(-)-4-methyl-2-(1-naphthylmethyl)imidazoline hydrochloride (3) is presented. The synthesis involves the prep...

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