Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

D13208

Sigma-Aldrich

1,4-Diaminobutane

99%

Synonym(s):

1,4-Butanediamine, Putrescine, Tetramethylenediamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
NH2(CH2)4NH2
CAS Number:
110-60-1
Molecular Weight:
88.15
Beilstein:
605282
EC Number:
203-782-3
MDL number:
MFCD00008235
UNSPSC Code:
12352100
PubChem Substance ID:
24893255
NACRES:
NA.22

Quality Level

200

Assay

99%

form

solid

expl. lim.

9.08 %

refractive index

n20/D 1.457 (lit.)

bp

158-160 °C (lit.)

mp

25-28 °C (lit.)

density

0.877 g/mL at 25 °C (lit.)

SMILES string

NCCCCN

InChI

1S/C4H12N2/c5-3-1-2-4-6/h1-6H2

InChI key

KIDHWZJUCRJVML-UHFFFAOYSA-N

Gene Information

rat ... Odc1(24609)

Looking for similar products? Visit Product Comparison Guide

Application

GABA precursor in many biological systems and synthon for amido-ureas.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H290,H302,H311,H314,H330

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

Flash Point(F)

113.0 °F - closed cup

Flash Point(C)

45 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH1830
BCCG8197
BCCG1932
BCCF5326
BCCD9230

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Journal of the Chemical Society. Perkin Transactions 1, 3179-3179 (1992)
M C de Mello et al.
Neurochemistry international, 22(3), 249-253 (1993-03-01)
Cultured retina cells from chick embryos took up [3H]putrescine and approx 10.8% of the incorporated amine was converted into [3H]GABA. The putrescine-derived GABA accumulated in a pool that was released in the medium at a rate corresponding to 3.66% of
Lingling Mao et al.
Journal of the American Chemical Society, 141(48), 19099-19109 (2019-11-08)
Hybrid halide double perovskites are a class of compounds attracting growing interest because of their richness of structure and property. Two-dimensional (2D) derivatives of hybrid double perovskites are formed by the incorporation of organic spacer cations into three-dimensional (3D) double
Juhani Jänne et al.
European journal of biochemistry, 271(5), 877-894 (2004-03-11)
The polyamines putrescine, spermidine and spermine are organic cations shown to participate in a bewildering number of cellular reactions, yet their exact functions in intermediary metabolism and specific interactions with cellular components remain largely elusive. Pharmacological interventions have demonstrated convincingly
Chi Yang et al.
PloS one, 7(10), e47314-e47314 (2012-10-17)
The phosphate starvation response in bacteria has been studied extensively for the past few decades and the phosphate-limiting signal is known to be mediated via the PhoBR two-component system. However, the global DNA binding profile of the response regulator PhoB
View All Related Papers

Protocols

HPLC Analysis of Biogenic Amines on Ascentis® RP-Amide

Separation of Histamine; Spermine; Spermidine; Tyramine; 1,4-Diaminobutane; Cadaverine

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service