Merck
CN

14960

Sigma-Aldrich

双(2-羟丙基)胺

≥98.0% (T)

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别名:
1,1′-亚氨基二-2-丙醇, 二异丙醇胺
线性分子式:
NH[CH2CH(OH)CH3]2
CAS号:
分子量:
133.19
Beilstein:
605363
EC 号:
MDL编号:
PubChem化学物质编号:

质量水平

检测方案

≥98.0% (T)

形式

solid

杂质

≤1% water

bp

249-250 °C/745 mmHg (lit.)

mp

42-45 °C (lit.)

溶解性

H2O: miscible
alcohol: miscible

密度

1.004 g/mL at 25 °C (lit.)

SMILES string

CC(O)CNCC(C)O

InChI

1S/C6H15NO2/c1-5(8)3-7-4-6(2)9/h5-9H,3-4H2,1-2H3

InChI key

LVTYICIALWPMFW-UHFFFAOYSA-N

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此商品
1102488.0326415156
Bis(2-hydroxypropyl)amine ≥98.0% (T)

Sigma-Aldrich

14960

双(2-羟丙基)胺

Amino-2-propanol 93%

Sigma-Aldrich

110248

1-氨基-2-丙醇

1,1-Iminodi-2-propanol for synthesis

Sigma-Aldrich

8.03264

1,1-Iminodi-2-propanol

Bispyrazolone for TLC derivatization, for the det.of cyanide, ≥98.0%

Supelco

15156

双吡唑啉酮

form

solid

form

-

form

solid

form

powder

bp

249-250 °C/745 mmHg (lit.)

bp

160 °C (lit.)

bp

249 °C/1013 hPa

bp

-

mp

42-45 °C (lit.)

mp

−2 °C (lit.)

mp

40.0-48.0 °C

mp

-

solubility

H2O: miscible, alcohol: miscible

solubility

-

solubility

870 g/L

solubility

formic acid: 50 mg/mL, clear, yellow

density

1.004 g/mL at 25 °C (lit.)

density

0.973 g/mL at 25 °C (lit.)

density

0.99 g/cm3 at 20 °C

density

-

应用

用双(2-羟丙基)胺(二异丙醇胺)研究了其对中国仓鼠卵巢(CHO)细胞胆碱摄取和磷脂合成的影响

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

275.0 °F - closed cup

闪点(°C)

135 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

危险化学品

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其他客户在看

Slide 1 of 7

1 of 7

Two cases of contact dermatitis due to diisopropanolamine.
Yoshihiro Umebayashi
The Journal of dermatology, 32(2), 145-146 (2005-05-24)
W T Stott et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46(2), 761-766 (2007-11-09)
Aminoalcohols differ in mammalian toxicity at least in part based upon their ability to alter the metabolism of phospholipids and to cause depletion of the essential nutrient choline in animals. This study examined the incorporation of diisopropanolamine (DIPA) into phospholipids
S A Saghir et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45(10), 2047-2056 (2007-06-23)
This study was conducted to determine the relative dermal bioavailability (absorption), distribution, metabolism, and excretion (ADME) of diisopropanolamine (DIPA), an alcohol amine used in a number of industrial and personal care products. Groups of 4 female Fischer 344 rats received
K A Johnson et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45(10), 1838-1845 (2007-05-18)
The repeated dose oral and dermal toxicity of diisopropanolamine (DIPA) was evaluated in rats and compared to the reported toxicity of the related secondary alcohol amine, diethanolamine (DEA). Fischer 344/DuCrl rats were given up to 750 mg/kg/day by dermal application
L M Gieg et al.
Canadian journal of microbiology, 45(5), 377-388 (1999-08-14)
Diisopropanolamine (DIPA) is a "sweetening agent" used to remove hydrogen sulfide from sour natural gas, and it is a contaminant at some sour gas treatment facilities in western Canada. To investigate the biodegradation of this alkanolamine, 14C-DIPA was used in

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