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A76001

(±)-3-氨基-1,2-丙二醇

Name: (±)-3-氨基-1,2-丙二醇
Brand: ALDRICH

97%

别名:

(±)-3-氨基-1,2-羟丙烷, 1-氨基甘油, 2,3-二羟丙烷-1-胺, 3-氨基-2-羟丙醇

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关于此项目

线性分子式:

NH₂CH₂CH(OH)CH₂OH

化学文摘社编号:

616-30-8

分子量:

91.11

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891256

EC Number:

210-475-8

Beilstein/REAXYS Number:

1719121

MDL number:

MFCD00008140

Assay:

97%

Form:

liquid

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属性

Quality Level

200

assay

97%

form

liquid

refractive index

n20/D 1.492 (lit.)

bp

264-265 °C/739 mmHg (lit.)

density

1.175 g/mL at 25 °C (lit.)

SMILES string

NCC(O)CO

InChI

1S/C3H9NO2/c4-1-3(6)2-5/h3,5-6H,1-2,4H2

InChI key

KQIGMPWTAHJUMN-UHFFFAOYSA-N

说明

Application

(±)-3-氨基-1,2-丙二醇是被用作合成用于RNA干扰（RNAi）治疗的脂质样递送分子（类脂质）的一种反应物。它还用于合成生物活性模板以制备阳离子α-螺旋多肽和各种阳离子聚合物用于基因递送。

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Competitive inhibition of lipolytic enzymes. II. Preparation of 'monoacylamino' phospholipids.

R Dijkman et al.

Biochimica et biophysica acta, 1043(1), 67-74 (1990-03-12)

This paper describes the synthesis of a number of phosphatidylcholines and phosphatidylglycols, in which one fatty acyl ester group is replaced by an acylamino function. The phospholipids, both of the alpha- and beta-type, are prepared in racemic and enantiomeric pure

A specific receptor site for glycerol, a new sweet tastant for Drosophila: structure-taste relationship of glycerol in the labellar sugar receptor cell.

Takaya Koseki et al.

Chemical senses, 29(8), 703-711 (2004-10-07)

Glycerol, a linear triol, is a sweet tastant for mammals but it has not previously been recognized to stimulate the sense of taste in insects. Here we show by electrophysiological experimentation that it effectively stimulates the labellar sugar receptor cell

Conversion of a hemoglobin alpha chain aspartate(47) ester to N-(2,3-dihydroxypropyl)asparagine as a method for identification of the principal binding site for benzo[a]pyrene anti-diol epoxide.

B W Day et al.

Chemical research in toxicology, 4(3), 359-363 (1991-05-01)

Human hemoglobin was alkylated with (+/-)-7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BPDE) and then treated with aqueous (+/-)-3-amino-1,2-propanediol to convert alkylated carboxyl side chains to N-(2,3-dihydroxypropyl) amides. Tryptic peptides produced from the modified protein were subjected to affinity chromatography on phenylboronic

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货号	GTIN
A76001-5G	04061837634925
A76001-100G	04061837634918
A76001-25G	04061833385296